<TR><TD>ABCA4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:370748">GDB:370748</A></TD><TD>1p13-1p13 1p22-1p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153800">MACULAR DEGENERATION, SENILE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248200">STARGARDT DISEASE 1; STGD1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601691">ATP BINDING CASSETTE TRANSPORTER; ABCR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601718">RETINITIS PIGMENTOSA-19; RP19</A><BR>
</TD>
</TR>
<TR><TD>ABCD3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131485">GDB:131485</A></TD><TD>1p22-1p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170995">PEROXISOMAL MEMBRANE PROTEIN 1; PXMP1</A><BR>
</TD>
</TR>
<TR><TD>ACADM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118958">GDB:118958</A></TD><TD>1p31-1p31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201450">ACYL-CoA DEHYDROGENASE, MEDIUM-CHAIN; ACADM</A><BR>
</TD>
</TR>
<TR><TD>AGL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132644">GDB:132644</A></TD><TD>1p21-1p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232400">GLYCOGEN STORAGE DISEASE III</A><BR>
</TD>
</TR>
<TR><TD>AGT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118750">GDB:118750</A></TD><TD>1q42-1q43 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106150">ANGIOTENSIN I; AGT</A><BR>
</TD>
</TR>
<TR><TD>ALDH4A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958827">GDB:9958827</A></TD><TD>1p36-1p36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=239510">HYPERPROLINEMIA, TYPE II</A><BR>
</TD>
</TR>
<TR><TD>ALPL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118730">GDB:118730</A></TD><TD>1p36.1-1p34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=171760">PHOSPHATASE, LIVER ALKALINE; ALPL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=241500">HYPOPHOSPHATASIA, INFANTILE</A><BR>
</TD>
</TR>
<TR><TD>AMPD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119677">GDB:119677</A></TD><TD>1p13-1p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=102770">ADENOSINE MONOPHOSPHATE DEAMINASE-1; AMPD1</A><BR>
</TD>
</TR>
<TR><TD>APOA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119685">GDB:119685</A></TD><TD>1q21-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107670">APOLIPOPROTEIN A-II; APOA2</A><BR>
</TD>
</TR>
<TR><TD>AVSD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265302">GDB:265302</A></TD><TD>1p31-1p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600309">ATRIOVENTRICULAR SEPTAL DEFECT; AVSD</A><BR>
</TD>
</TR>
<TR><TD>BRCD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955322">GDB:9955322</A></TD><TD>1p36-1p36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=211420">BREAST CANCER, DUCTAL, 2; BRCD2</A><BR>
</TD>
</TR>
<TR><TD>C1QA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119042">GDB:119042</A></TD><TD>1p36.3-1p34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120550">COMPLEMENT COMPONENT 1, q SUBCOMPONENT, ALPHA POLYPEPTIDE; C1QA</A><BR>
</TD>
</TR>
<TR><TD>C1QB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119043">GDB:119043</A></TD><TD>1p36.3-1p34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120570">COMPLEMENT COMPONENT 1, q SUBCOMPONENT, BETA POLYPEPTIDE; C1QB</A><BR>
</TD>
</TR>
<TR><TD>C1QG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128132">GDB:128132</A></TD><TD>1p36.3-1p34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120575">COMPLEMENT COMPONENT 1, q SUBCOMPONENT, GAMMA POLYPEPTIDE; C1QG</A><BR>
</TD>
</TR>
<TR><TD>C8A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119735">GDB:119735</A></TD><TD>1p32-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120950">COMPLEMENT COMPONENT-8, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>C8B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119736">GDB:119736</A></TD><TD>1p32-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120960">COMPLEMENT COMPONENT-8, DEFICIENCY OF, TYPE II</A><BR>
</TD>
</TR>
<TR><TD>CACNA1S</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126431">GDB:126431</A></TD><TD>1q31-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114208">CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA 1S SUBUNIT; CACNA1S</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170400">PERIODIC PARALYSIS I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601887">MALIGNANT HYPERTHERMIA SUSCEPTIBILITY-5; MHS5</A><BR>
</TD>
</TR>
<TR><TD>CCV</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1336655">GDB:1336655</A></TD><TD>1p36-1p36 1p36.3-1p36.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115665">CATARACT, CONGENITAL, VOLKMANN TYPE; CCV</A><BR>
</TD>
</TR>
<TR><TD>CD3Z</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119766">GDB:119766</A></TD><TD>1q22-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186780">CD3Z ANTIGEN, ZETA POLYPEPTIDE; CD3Z</A><BR>
</TD>
</TR>
<TR><TD>CDC2L1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127827">GDB:127827</A></TD><TD>1p36-1p36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176873">PROTEIN KINASE p58; PK58</A><BR>
</TD>
</TR>
<TR><TD>CHML</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135222">GDB:135222</A></TD><TD>1q31-1qter 1q42-1qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118825">CHOROIDEREMIA-LIKE; CHML</A><BR>
</TD>
</TR>
<TR><TD>CHS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4568202">GDB:4568202</A></TD><TD>1q42.1-1q42.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214500">CHEDIAK-HIGASHI SYNDROME; CHS1</A><BR>
</TD>
</TR>
<TR><TD>CIAS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957338">GDB:9957338</A></TD><TD>1q43-1q44 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120100">COLD HYPERSENSITIVITY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191900">URTICARIA, DEAFNESS, AND AMYLOIDOSIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606416"></A><BR>
</TD>
</TR>
<TR><TD>CLCNKB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:698472">GDB:698472</A></TD><TD>1p36-1p36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602023">CHLORIDE CHANNEL, KIDNEY, B; CLCNKB</A><BR>
</TD>
</TR>
<TR><TD>CMD1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:434478">GDB:434478</A></TD><TD>1p1-1q1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115200">CARDIOMYOPATHY, DILATED 1A; CMD1A</A><BR>
</TD>
</TR>
<TR><TD>CMH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:137324">GDB:137324</A></TD><TD>1q3-1q3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115195">CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 2; CMH2</A><BR>
</TD>
</TR>
<TR><TD>CMM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119059">GDB:119059</A></TD><TD>1p36-1p36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=155600">MELANOMA, MALIGNANT</A><BR>
</TD>
</TR>
<TR><TD>COL11A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120595">GDB:120595</A></TD><TD>1p21-1p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120280">COLLAGEN, TYPE XI, ALPHA-1; COL11A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604841"></A><BR>
</TD>
</TR>
<TR><TD>COL8A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127812">GDB:127812</A></TD><TD>1p34.3-1p32.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120252">COLLAGEN, TYPE VIII, ALPHA-2 POLYPEPTIDE; COL8A2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122000">CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR; PPCD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136800">FUCHS ENDOTHELIAL DYSTROPHY OF THE CORNEA</A><BR>
</TD>
</TR>
<TR><TD>COL9A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138310">GDB:138310</A></TD><TD>1p33-1p32.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120260">COLLAGEN, TYPE IX, ALPHA-2 CHAIN; COL9A2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600204">EPIPHYSEAL DYSPLASIA, MULTIPLE, 2; EDM2</A><BR>
</TD>
</TR>
<TR><TD>CPT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127272">GDB:127272</A></TD><TD>1p32-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=255110">MYOPATHY WITH DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE II</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600649">HYPOGLYCEMIA, HYPOKETOTIC, WITH DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600650">CARNITINE PALMITOYLTRANSFERASE II; CPT2</A><BR>
</TD>
</TR>
<TR><TD>CRB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:333930">GDB:333930</A></TD><TD>1q31-1q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600105">RETINITIS PIGMENTOSA-12; RP12</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604210"></A><BR>
</TD>
</TR>
<TR><TD>CSE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:596182">GDB:596182</A></TD><TD>1p-1p 1p31-1p31 1p33-1p32.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601042">CHOREOATHETOSIS/SPASTICITY, EPISODIC; CSE</A><BR>
</TD>
</TR>
<TR><TD>CSF3R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126430">GDB:126430</A></TD><TD>1p35-1p34.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138971">COLONY STIMULATING FACTOR 3 RECEPTOR, GRANULOCYTE; CSF3R</A><BR>
</TD>
</TR>
<TR><TD>CTPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9863168">GDB:9863168</A></TD><TD>1pter-1p36.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=116600">CATARACT, POSTERIOR POLAR</A><BR>
</TD>
</TR>
<TR><TD>CTSK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:453910">GDB:453910</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=265800">PYCNODYSOSTOSIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601105">CATHEPSIN K; CTSK</A><BR>
</TD>
</TR>
<TR><TD>DBT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118784">GDB:118784</A></TD><TD>1p31-1p31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248610">MAPLE SYRUP URINE DISEASE, TYPE 2</A><BR>
</TD>
</TR>
<TR><TD>DIO1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136449">GDB:136449</A></TD><TD>1p33-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147892">THYROXINE DEIODINASE TYPE I; TXDI1</A><BR>
</TD>
</TR>
<TR><TD>DISC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9992707">GDB:9992707</A></TD><TD>1q42.1-1q42.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181500">DISORDER-2; SCZD2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605210"></A><BR>
</TD>
</TR>
<TR><TD>DPYD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:364102">GDB:364102</A></TD><TD>1p22-1p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=274270">DIHYDROPYRIMIDINE DEHYDROGENASE; DPYD</A><BR>
</TD>
</TR>
<TR><TD>EKV</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119106">GDB:119106</A></TD><TD>1pter-1qter 1p35.1-1p35.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133200">ERYTHROKERATODERMIA VARIABILIS; EKV</A><BR>
</TD>
</TR>
<TR><TD>ENO1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119871">GDB:119871</A></TD><TD>1p36-1p36 1pter-1p36.13 1p36.3-1p36.2 1p36.2-1p36.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172430">PHOSPHOPYRUVATE HYDRATASE; PPH</A><BR>
</TD>
</TR>
<TR><TD>ENO1P</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135006">GDB:135006</A></TD><TD>1pter-1qter 1q41-1q42 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172430">PHOSPHOPYRUVATE HYDRATASE; PPH</A><BR>
</TD>
</TR>
<TR><TD>EPB41</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119865">GDB:119865</A></TD><TD>1p34.2-1p33 1p36.2-1p34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130500">ERYTHROCYTE MEMBRANE PROTEIN BAND 4.1; EPB41</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166900">HEREDITARY HEMOLYTIC</A><BR>
</TD>
</TR>
<TR><TD>EPHX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119876">GDB:119876</A></TD><TD>1p11-1qter 1q42.1-1q42.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=132810">EPOXIDE HYDROLASE 1, MICROSOMAL; EPHX1</A><BR>
</TD>
</TR>
<TR><TD>F13B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119893">GDB:119893</A></TD><TD>1q31-1q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134580">FACTOR XIII, B SUBUNIT; F13B</A><BR>
</TD>
</TR>
<TR><TD>F5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119896">GDB:119896</A></TD><TD>1q21-1q25 1q23-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227400">FACTOR V DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>FCGR2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119903">GDB:119903</A></TD><TD>1q23-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146790">Fc FRAGMENT OF IgG, LOW AFFINITY IIa, RECEPTOR FOR; FCGR2A</A><BR>
</TD>
</TR>
<TR><TD>FCGR2B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128183">GDB:128183</A></TD><TD>1q23-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146790">Fc FRAGMENT OF IgG, LOW AFFINITY IIa, RECEPTOR FOR; FCGR2A</A><BR>
</TD>
</TR>
<TR><TD>FCGR3A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119904">GDB:119904</A></TD><TD>1q23-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146740">Fc FRAGMENT OF IgG, LOW AFFINITY IIIa, RECEPTOR FOR; FCGR3A</A><BR>
</TD>
</TR>
<TR><TD>FCHL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9837503">GDB:9837503</A></TD><TD>1q21-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=144250">HYPERLIPIDEMIA, COMBINED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602491"></A><BR>
</TD>
</TR>
<TR><TD>FH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119133">GDB:119133</A></TD><TD>1q42.1-1q42.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136850">FUMARATE HYDRATASE; FH</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150800">LEIOMYOMATA, HEREDITARY MULTIPLE, OF SKIN</A><BR>
</TD>
</TR>
<TR><TD>FMO3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135136">GDB:135136</A></TD><TD>1q-1q 1q23-1q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136132">FLAVIN-CONTAINING MONOOXYGENASE 3; FMO3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602079">TRIMETHYLAMINURIA</A><BR>
</TD>
</TR>
<TR><TD>FMO4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127981">GDB:127981</A></TD><TD>1q-1q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136131">FLAVIN-CONTAINING MONOOXYGENASE 2; FMO2</A><BR>
</TD>
</TR>
<TR><TD>FUCA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119237">GDB:119237</A></TD><TD>1p34-1p34 1p35-1p34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230000">FUCOSIDOSIS</A><BR>
</TD>
</TR>
<TR><TD>FY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119242">GDB:119242</A></TD><TD>1q22-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=110700">BLOOD GROUP--DUFFY SYSTEM; Fy</A><BR>
</TD>
</TR>
<TR><TD>GALE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119245">GDB:119245</A></TD><TD>1p36-1p35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230350">GALACTOSE EPIMERASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>GBA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119262">GDB:119262</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230800">GAUCHER DISEASE, TYPE I; GD I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606463"></A><BR>
</TD>
</TR>
<TR><TD>GFND</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958222">GDB:9958222</A></TD><TD>1q32-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601894">GLOMERULAR NEPHRITIS, FAMILIAL, WITH FIBRONECTIN DEPOSITS</A><BR>
</TD>
</TR>
<TR><TD>GJA8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:696369">GDB:696369</A></TD><TD>1q21-1q25 1pter-1qter 1q21.1-1q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=116200">CATARACT, ZONULAR PULVERULENT 1; CZP1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600897">GAP JUNCTION PROTEIN, ALPHA-8, 50-KD; GJA8</A><BR>
</TD>
</TR>
<TR><TD>GJB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127820">GDB:127820</A></TD><TD>1p35-1p33 1p35.1-1p35.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133200">ERYTHROKERATODERMIA VARIABILIS; EKV</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600101">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 2; DFNA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603324"></A><BR>
</TD>
</TR>
<TR><TD>GLC3B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3801939">GDB:3801939</A></TD><TD>1p36-1p36 1p36.2-1p36.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600975">GLAUCOMA 3, PRIMARY INFANTILE, B; GLC3B</A><BR>
</TD>
</TR>
<TR><TD>HF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120041">GDB:120041</A></TD><TD>1q32-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134370">H FACTOR 1; HF1</A><BR>
</TD>
</TR>
<TR><TD>HMGCL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138445">GDB:138445</A></TD><TD>1p36.1-1p35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=246450">HYDROXYMETHYLGLUTARICACIDURIA; HMGCL</A><BR>
</TD>
</TR>
<TR><TD>HPC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5215209">GDB:5215209</A></TD><TD>1q24-1q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176807">PROSTATE CANCER; PRCA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601518">PROSTATE CANCER, HEREDITARY 1</A><BR>
</TD>
</TR>
<TR><TD>HRD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9862254">GDB:9862254</A></TD><TD>1q42-1q43 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=241410">HYPOPARATHYROIDISM WITH SHORT STATURE, MENTAL RETARDATION, AND SEIZURES</A><BR>
</TD>
</TR>
<TR><TD>HRPT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125253">GDB:125253</A></TD><TD>1q21-1q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145001">HYPERPARATHYROIDISM, FAMILIAL PRIMARY, WITH MULTIPLE OSSIFYING JAW</A><BR>
</TD>
</TR>
<TR><TD>HSD3B2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134044">GDB:134044</A></TD><TD>1p13.1-1p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201810">ADRENAL HYPERPLASIA II</A><BR>
</TD>
</TR>
<TR><TD>HSPG2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126372">GDB:126372</A></TD><TD>1p36.1-1p35 1p36.1-1p36.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142461">HEPARAN SULFATE PROTEOGLYCAN OF BASEMENT MEMBRANE; HSPG2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=255800">MYOTONIC MYOPATHY, DWARFISM, CHONDRODYSTROPHY, AND OCULAR AND FACIAL</A><BR>
</TD>
</TR>
<TR><TD>KCNQ4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439046">GDB:439046</A></TD><TD>1p-1p 1p34-1p32 1p34-1p34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600101">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 2; DFNA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603537"></A><BR>
</TD>
</TR>
<TR><TD>KCS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9848740">GDB:9848740</A></TD><TD>1q42-1q43 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=244460">KENNY-CAFFEY SYNDROME, RECESSIVE FORM</A><BR>
</TD>
</TR>
<TR><TD>KIF1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128645">GDB:128645</A></TD><TD>1p36-1p36 1p36.22-1p36.22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118210">CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, A; CMT2A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605995"></A><BR>
</TD>
</TR>
<TR><TD>LAMB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:251820">GDB:251820</A></TD><TD>1q32-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150310">LAMININ, BETA 3; LAMB3</A><BR>
</TD>
</TR>
<TR><TD>LAMC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136225">GDB:136225</A></TD><TD>1q31-1q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150292">LAMININ, GAMMA 2; LAMC2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=226700">EPIDERMOLYSIS BULLOSA LETALIS</A><BR>
</TD>
</TR>
<TR><TD>LGMD1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:231606">GDB:231606</A></TD><TD>1q11-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159001">MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B; LGMD1B</A><BR>
</TD>
</TR>
<TR><TD>LMNA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132146">GDB:132146</A></TD><TD>1q21.2-1q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150330">LAMIN A/C; LMNA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151660">LIPODYSTROPHY, FAMILIAL PARTIAL, DUNNIGAN TYPE; LDP1</A><BR>
</TD>
</TR>
<TR><TD>LOR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132049">GDB:132049</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=152445">LORICRIN; LOR</A><BR>
</TD>
</TR>
<TR><TD>MCKD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9859381">GDB:9859381</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=174000">POLYCYSTIC KIDNEYS, MEDULLARY TYPE</A><BR>
</TD>
</TR>
<TR><TD>MCL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:139137">GDB:139137</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159552">MYELOID CELL LEUKEMIA 1; MCL1</A><BR>
</TD>
</TR>
<TR><TD>MPZ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125266">GDB:125266</A></TD><TD>1q22-1q22 1q22-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145900">HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159440">MYELIN PROTEIN ZERO; MPZ</A><BR>
</TD>
</TR>
<TR><TD>MTHFR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:370882">GDB:370882</A></TD><TD>1p36.3-1p36.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=236250">5,10-@METHYLENETETRAHYDROFOLATE REDUCTASE; MTHFR</A><BR>
</TD>
</TR>
<TR><TD>MTR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119440">GDB:119440</A></TD><TD>1pter-1qter 1q43-1q43 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156570">METHYLTETRAHYDROFOLATE:L-HOMOCYSTEINE S-METHYLTRANSFERASE; MTR</A><BR>
</TD>
</TR>
<TR><TD>MUTYH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9315115">GDB:9315115</A></TD><TD>1p34.3-1p32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=175100">ADENOMATOUS POLYPOSIS OF THE COLON; APC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604933"></A><BR>
</TD>
</TR>
<TR><TD>MYOC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5584221">GDB:5584221</A></TD><TD>1q23-1q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137750">GLAUCOMA 1, OPEN ANGLE; GLC1A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601652">MYOCILIN; MYOC</A><BR>
</TD>
</TR>
<TR><TD>NB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958705">GDB:9958705</A></TD><TD>1p36.3-1p36.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256700">NEUROBLASTOMA; NB</A><BR>
</TD>
</TR>
<TR><TD>NCF2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120223">GDB:120223</A></TD><TD>1cen-1q32 1q25-1q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=233710">GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-POSITIVE FORM</A><BR>
</TD>
</TR>
<TR><TD>NEM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127387">GDB:127387</A></TD><TD>1q22-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=161800">NEMALINE MYOPATHY 1, AUTOSOMAL DOMINANT; NEM1</A><BR>
</TD>
</TR>
<TR><TD>NPHS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955617">GDB:9955617</A></TD><TD>1q25-1q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600995">ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2; ARVD2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604766"></A><BR>
</TD>
</TR>
<TR><TD>NPPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118727">GDB:118727</A></TD><TD>1p36-1p36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108780">NATRIURETIC PEPTIDE PRECURSOR A; NPPA</A><BR>
</TD>
</TR>
<TR><TD>NRAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119457">GDB:119457</A></TD><TD>1p13-1p13 1p13.1-1p13.1 1p13.2-1p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164790">ONCOGENE NRAS; NRAS; NRAS1</A><BR>
</TD>
</TR>
<TR><TD>NTRK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127897">GDB:127897</A></TD><TD>1q21-1q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164970">ONCOGENE TRK</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191315">NEUROTROPHIC TYROSINE KINASE, RECEPTOR, TYPE 1; NTRK1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256800">NEUROPATHY, CONGENITAL SENSORY, WITH ANHIDROSIS</A><BR>
</TD>
</TR>
<TR><TD>OPTA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955577">GDB:9955577</A></TD><TD>1p21-1p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166600">OSTEOPETROSIS, AUTOSOMAL DOMINANT, TYPE II; OPA2</A><BR>
</TD>
</TR>
<TR><TD>PBX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125351">GDB:125351</A></TD><TD>1q23-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176310">PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR-1; PBX1</A><BR>
</TD>
</TR>
<TR><TD>PCHC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955586">GDB:9955586</A></TD><TD>1p-1p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=171300">PHEOCHROMOCYTOMA</A><BR>
</TD>
</TR>
<TR><TD>PGD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119486">GDB:119486</A></TD><TD>1p36.2-1p36.13 1p36.3-1p36.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172200">6-@PHOSPHOGLUCONATE DEHYDROGENASE, ERYTHROCYTE</A><BR>
</TD>
</TR>
<TR><TD>PHA2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955628">GDB:9955628</A></TD><TD>1q31-1q42 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145260">PSEUDOHYPOALDOSTERONISM, TYPE II; PHA2</A><BR>
</TD>
</TR>
<TR><TD>PHGDH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958261">GDB:9958261</A></TD><TD>1-1 1p12-1p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601815">3-@PHOSPHOGLYCERATE DEHYDROGENASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>PKLR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120294">GDB:120294</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266200">PYRUVATE KINASE DEFICIENCY OF ERYTHROCYTE</A><BR>
</TD>
</TR>
<TR><TD>PKP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4249598">GDB:4249598</A></TD><TD>1q-1q 1q32-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601975">PLAKOPHILIN 1; PKP1</A><BR>
</TD>
</TR>
<TR><TD>PLA2G2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120296">GDB:120296</A></TD><TD>1p35-1p35 1p36.1-1p35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172411">PHOSPHOLIPASE A2, GROUP IIA; PLA2G2A</A><BR>
</TD>
</TR>
<TR><TD>PLOD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127821">GDB:127821</A></TD><TD>1p36.3-1p36.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153454">PROCOLLAGEN-LYSINE, 2-OXOGLUTARATE 5-DIOXYGENASE; PLOD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=225400">EHLERS-DANLOS SYNDROME, TYPE VI; E-D VI; EDS VI</A><BR>
</TD>
</TR>
<TR><TD>PPOX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118852">GDB:118852</A></TD><TD>1q22-1q22 1q23-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600923">PROTOPORPHYRINOGEN OXIDASE; PPOX</A><BR>
</TD>
</TR>
<TR><TD>PPT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125227">GDB:125227</A></TD><TD>1p32-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256730">CEROID-LIPOFUSCINOSIS, NEURONAL 1, INFANTILE; CLN1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600722">PALMITOYL-PROTEIN THIOESTERASE; PPT</A><BR>
</TD>
</TR>
<TR><TD>PRCC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3888215">GDB:3888215</A></TD><TD>1q21.2-1q21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179755">PAPILLARY RENAL CELL CARCINOMA; PRCC</A><BR>
</TD>
</TR>
<TR><TD>PRG4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955719">GDB:9955719</A></TD><TD>1q24-1q25 1q25-1q31.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=208250">ARTHROPATHY-CAMPTODACTYLY SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604283"></A><BR>
</TD>
</TR>
<TR><TD>PSEN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:633044">GDB:633044</A></TD><TD>1q31-1q42 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600759">ALZHEIMER DISEASE, FAMILIAL, TYPE 4; AD4</A><BR>
</TD>
</TR>
<TR><TD>PTOS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6279920">GDB:6279920</A></TD><TD>1p34.1-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=178300">PTOSIS, HEREDITARY CONGENITAL 1; PTOS1</A><BR>
</TD>
</TR>
<TR><TD>REN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120345">GDB:120345</A></TD><TD>1q32-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179820">RENIN; REN</A><BR>
</TD>
</TR>
<TR><TD>RFX5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6288464">GDB:6288464</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601863">REGULATORY FACTOR 5; RFX5</A><BR>
</TD>
</TR>
<TR><TD>RHD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119551">GDB:119551</A></TD><TD>1p36.2-1p34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=111680">RHESUS BLOOD GROUP, D ANTIGEN; RHD</A><BR>
</TD>
</TR>
<TR><TD>RMD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:448902">GDB:448902</A></TD><TD>1q41-1q41 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600332">RIPPLING MUSCLE DISEASE-1; RMD1</A><BR>
</TD>
</TR>
<TR><TD>RPE65</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:226519">GDB:226519</A></TD><TD>1p31-1p31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180069">RETINAL PIGMENT EPITHELIUM-SPECIFIC PROTEIN, 65-KD; RPE65</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204100">AMAUROSIS CONGENITA OF LEBER II</A><BR>
</TD>
</TR>
<TR><TD>SCCD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955558">GDB:9955558</A></TD><TD>1p36-1p34.1 1p36.3-1p36.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121800">CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER</A><BR>
</TD>
</TR>
<TR><TD>SERPINC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119024">GDB:119024</A></TD><TD>1q23-1q25.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107300">ANTITHROMBIN III DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>SJS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1381631">GDB:1381631</A></TD><TD>1p36-1p36 1p36.1-1p34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=255800">MYOTONIC MYOPATHY, DWARFISM, CHONDRODYSTROPHY, AND OCULAR AND FACIAL</A><BR>
</TD>
</TR>
<TR><TD>SLC19A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9837779">GDB:9837779</A></TD><TD>1q23.2-1q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=60394"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=249270">THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>SLC2A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120627">GDB:120627</A></TD><TD>1p35-1p31.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138140">SOLUTE CARRIER FAMILY 2, MEMBER 1; SLC2A1</A><BR>
</TD>
</TR>
<TR><TD>SPG23</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11523305">GDB:11523305</A></TD><TD>1q24-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=270750">PARAPLEGIA WITH PIGMENTARY ABNORMALITIES</A><BR>
</TD>
</TR>
<TR><TD>SPTA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119601">GDB:119601</A></TD><TD>1q21-1q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130600">ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166900">HEREDITARY HEMOLYTIC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182860">SPECTRIN, ALPHA, ERYTHROCYTIC 1; SPTA1</A><BR>
</TD>
</TR>
<TR><TD>TAL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120759">GDB:120759</A></TD><TD>1p32-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=187040">T-CELL ACUTE LYMPHOCYTIC LEUKEMIA 1; TAL1</A><BR>
</TD>
</TR>
<TR><TD>TNFSF6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:422178">GDB:422178</A></TD><TD>1q23-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134638">APOPTOSIS ANTIGEN LIGAND 1; APT1LG1</A><BR>
</TD>
</TR>
<TR><TD>TNNT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:221879">GDB:221879</A></TD><TD>1q3-1q3 1q32-1q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191045">TROPONIN-T2, CARDIAC; TNNT2</A><BR>
</TD>
</TR>
<TR><TD>TPM3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127872">GDB:127872</A></TD><TD>1q22-1q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164970">ONCOGENE TRK</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191030">TROPOMYOSIN 3; TPM3</A><BR>
</TD>
</TR>
<TR><TD>TSHB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120467">GDB:120467</A></TD><TD>1p13-1p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188540">THYROID-STIMULATING HORMONE, BETA CHAIN; TSHB</A><BR>
</TD>
</TR>
<TR><TD>UMPK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120481">GDB:120481</A></TD><TD>1p32-1p32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191710">URIDINE MONOPHOSPHATE KINASE; UMPK</A><BR>
</TD>
</TR>
<TR><TD>UOX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127539">GDB:127539</A></TD><TD>1p22-1p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191540">URATE OXIDASE; UOX</A><BR>
</TD>
</TR>
<TR><TD>UROD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119628">GDB:119628</A></TD><TD>1p34-1p34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176100">PORPHYRIA CUTANEA TARDA; PCT</A><BR>
</TD>
</TR>
<TR><TD>USH2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120483">GDB:120483</A></TD><TD>1q41-1q41 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276901">USHER SYNDROME, TYPE II; USH2</A><BR>
</TD>
</TR>
<TR><TD>VMGLOM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958134">GDB:9958134</A></TD><TD>1p22-1p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138000">GLOMUS TUMORS, MULTIPLE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601749">FKBP-ASSOCIATED 48-KD PROTEIN</A><BR>
</TD>
</TR>
<TR><TD>VWS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120532">GDB:120532</A></TD><TD>1q32-1q32 1q32-1q42 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=119300">CLEFT LIP AND/OR PALATE WITH MUCOUS CYSTS OF LOWER LIP</A><BR>
</TD>
</TR>
<TR><TD>WS2B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:407579">GDB:407579</A></TD><TD>1p21-1p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600193">WAARDENBURG SYNDROME, TYPE 2B; WS2B</A><BR>
</TD>
</TR>
<TR><TD>ABCB11</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864786">GDB:9864786</A></TD><TD>2q24-2q24 2q24.3-2q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601847">CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 2; PFIC2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603201"></A><BR>
</TD>
</TR>
<TR><TD>ABCG5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10450298">GDB:10450298</A></TD><TD>2p21-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=210250">PHYTOSTEROLEMIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605459"></A><BR>
</TD>
</TR>
<TR><TD>ABCG8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10450300">GDB:10450300</A></TD><TD>2p21-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=210250">PHYTOSTEROLEMIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605460"></A><BR>
</TD>
</TR>
<TR><TD>ACADL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118745">GDB:118745</A></TD><TD>2q34-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201460">ACYL-CoA DEHYDROGENASE, LONG-CHAIN, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>ACP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118962">GDB:118962</A></TD><TD>2p25-2p25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=171500">PHOSPHATASE, ACID, OF ERYTHROCYTE; ACP1</A><BR>
</TD>
</TR>
<TR><TD>AGXT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127113">GDB:127113</A></TD><TD>2q37.3-2q37.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=259900">OXALOSIS I</A><BR>
</TD>
</TR>
<TR><TD>AHHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118984">GDB:118984</A></TD><TD>2pter-2q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108330">CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 1; CYP1A1</A><BR>
</TD>
</TR>
<TR><TD>ALMS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9865539">GDB:9865539</A></TD><TD>2p13-2p12 2p14-2p13 2p13.1-2p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203800">ALSTROM SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>ALPP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119672">GDB:119672</A></TD><TD>2q37.1-2q37.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=171800">ALKALINE PHOSPHATASE, PLACENTAL; ALPP</A><BR>
</TD>
</TR>
<TR><TD>ALS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135696">GDB:135696</A></TD><TD>2q33-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=205100">AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE; ALS2</A><BR>
</TD>
</TR>
<TR><TD>APOB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119686">GDB:119686</A></TD><TD>2p24-2p23 2p24-2p24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107730">APOLIPOPROTEIN B; APOB</A><BR>
</TD>
</TR>
<TR><TD>BDE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955730">GDB:9955730</A></TD><TD>2q37-2q37 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113300">BRACHYDACTYLY, TYPE E; BDE</A><BR>
</TD>
</TR>
<TR><TD>BDMR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:533064">GDB:533064</A></TD><TD>2q37-2q37 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600430">BRACHYDACTYLY-MENTAL RETARDATION SYNDROME; BDMR</A><BR>
</TD>
</TR>
<TR><TD>BJS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955717">GDB:9955717</A></TD><TD>2q34-2q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=262000">TORTI AND NERVE DEAFNESS</A><BR>
</TD>
</TR>
<TR><TD>BMPR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:642243">GDB:642243</A></TD><TD>2q33-2q33 2q33-2q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=178600">PULMONARY HYPERTENSION, PRIMARY; PPH1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600799">BONE MORPHOGENETIC RECEPTOR TYPE II; BMPR2</A><BR>
</TD>
</TR>
<TR><TD>CHRNA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120586">GDB:120586</A></TD><TD>2q24-2q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100690">CHOLINERGIC RECEPTOR, NICOTINIC, ALPHA POLYPEPTIDE 1; CHRNA1</A><BR>
</TD>
</TR>
<TR><TD>CMCWTD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498919">GDB:11498919</A></TD><TD>2p22.3-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114580">FAMILIAL CHRONIC MUCOCUTANEOUS, DOMINANT TYPE</A><BR>
</TD>
</TR>
<TR><TD>CNGA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:434398">GDB:434398</A></TD><TD>2q11.2-2q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=216900">COLORBLINDNESS, TOTAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600053">CYCLIC NUCLEOTIDE GATED CHANNEL, OLFACTORY, 3; CNG3</A><BR>
</TD>
</TR>
<TR><TD>COL3A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118729">GDB:118729</A></TD><TD>2q31-2q32.3 2q32.2-2q32.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120180">COLLAGEN, TYPE III; COL3A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130050">EHLERS-DANLOS SYNDROME, TYPE IV, AUTOSOMAL DOMINANT</A><BR>
</TD>
</TR>
<TR><TD>COL4A3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128351">GDB:128351</A></TD><TD>2q36-2q37 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120070">COLLAGEN, TYPE IV, ALPHA-3 CHAIN; COL4A3</A><BR>
</TD>
</TR>
<TR><TD>COL4A4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132673">GDB:132673</A></TD><TD>2q35-2q37 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120131">COLLAGEN, TYPE IV, ALPHA-4 CHAIN; COL4A4</A><BR>
</TD>
</TR>
<TR><TD>COL6A3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119066">GDB:119066</A></TD><TD>2q37.3-2q37.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120250">COLLAGEN, TYPE VI, ALPHA-3 CHAIN; COL6A3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158810">MYOPATHY, BENIGN CONGENITAL, WITH CONTRACTURES</A><BR>
</TD>
</TR>
<TR><TD>CPS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119799">GDB:119799</A></TD><TD>2q33-2q36 2q34-2q35 2q35-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=237300">HYPERAMMONEMIA DUE TO CARBAMOYLPHOSPHATE SYNTHETASE I DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>CRYGA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119076">GDB:119076</A></TD><TD>2q33-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123660">CRYSTALLIN, GAMMA A; CRYGA</A><BR>
</TD>
</TR>
<TR><TD>CRYGEP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119808">GDB:119808</A></TD><TD>2q33-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123660">CRYSTALLIN, GAMMA A; CRYGA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604307"></A><BR>
</TD>
</TR>
<TR><TD>CYP1B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:353515">GDB:353515</A></TD><TD>2p21-2p21 2p22-2p21 2pter-2qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231300">GLAUCOMA 3, PRIMARY INFANTILE, A; GLC3A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601771">CYTOCHROME P450, SUBFAMILY I (DIOXIN-INDUCIBLE), POLYPEPTIDE 1; CYP1B1</A><BR>
</TD>
</TR>
<TR><TD>CYP27A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128129">GDB:128129</A></TD><TD>2q33-2qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=213700">CEREBROTENDINOUS XANTHOMATOSIS</A><BR>
</TD>
</TR>
<TR><TD>DBI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119837">GDB:119837</A></TD><TD>2q12-2q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125950">DIAZEPAM BINDING INHIBITOR; DBI</A><BR>
</TD>
</TR>
<TR><TD>DES</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119841">GDB:119841</A></TD><TD>2q35-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125660">DESMIN; DES</A><BR>
</TD>
</TR>
<TR><TD>DYSF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:340831">GDB:340831</A></TD><TD>2p-2p 2p13-2p13 2pter-2p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253601">MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B; LGMD2B</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254130">MUSCULAR DYSTROPHY, LATE-ONSET DISTAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603009"></A><BR>
</TD>
</TR>
<TR><TD>EDAR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9837372">GDB:9837372</A></TD><TD>2q11-2q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=129490">DYSPLASIA, HYPOHIDROTIC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=224900">ECTODERMAL DYSPLASIA, ANHIDROTIC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604095"></A><BR>
</TD>
</TR>
<TR><TD>EFEMP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1220111">GDB:1220111</A></TD><TD>2p16-2p16 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126600">DOYNE HONEYCOMB DEGENERATION OF RETINA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601548">FIBRILLIN-LIKE; FBNL</A><BR>
</TD>
</TR>
<TR><TD>EIF2AK3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956743">GDB:9956743</A></TD><TD>2p12-2p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=226980">EPIPHYSEAL DYSPLASIA, MULTIPLE, WITH EARLY-ONSET DIABETES MELLITUS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604032"></A><BR>
</TD>
</TR>
<TR><TD>ERCC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119881">GDB:119881</A></TD><TD>2q21-2q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133510">EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 3; ERCC3</A><BR>
</TD>
</TR>
<TR><TD>FSHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127510">GDB:127510</A></TD><TD>2p21-2p16 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136435">FOLLICLE-STIMULATING HORMONE RECEPTOR; FSHR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=233300">GONADAL DYSGENESIS, XX TYPE</A><BR>
</TD>
</TR>
<TR><TD>GINGF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9848875">GDB:9848875</A></TD><TD>2p21-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=135300">GINGIVAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182530">SON OF SEVENLESS (DROSOPHILA) HOMOLOG 1; SOS1</A><BR>
</TD>
</TR>
<TR><TD>GLC1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1297553">GDB:1297553</A></TD><TD>2q1-2q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137760">GLAUCOMA 1, OPEN ANGLE, B; GLC1B</A><BR>
</TD>
</TR>
<TR><TD>GPD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:354558">GDB:354558</A></TD><TD>2q24.1-2q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138430">GLYCEROL-3-PHOSPHATE DEHYDROGENASE-2; GPD2</A><BR>
</TD>
</TR>
<TR><TD>GYPC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120027">GDB:120027</A></TD><TD>2q14-2q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=110750">BLOOD GROUP--GERBICH; Ge</A><BR>
</TD>
</TR>
<TR><TD>HADHA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:434026">GDB:434026</A></TD><TD>2p23-2p23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600890">HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE,</A><BR>
</TD>
</TR>
<TR><TD>HADHB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:344953">GDB:344953</A></TD><TD>2p23-2p23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143450">HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE,</A><BR>
</TD>
</TR>
<TR><TD>HOXD13</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127225">GDB:127225</A></TD><TD>2q31-2q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142989">HOMEO BOX-D13; HOXD13</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186000">SYNDACTYLY, TYPE II</A><BR>
</TD>
</TR>
<TR><TD>HPE2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136066">GDB:136066</A></TD><TD>2p21-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157170">MIDLINE CLEFT SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>IGKC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120088">GDB:120088</A></TD><TD>2p12-2p12 2p11.2-2p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147200">IMMUNOGLOBULIN KAPPA CONSTANT REGION; IGKC</A><BR>
</TD>
</TR>
<TR><TD>IHH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:511203">GDB:511203</A></TD><TD>2q33-2q35 2q35-2q35 2pter-2qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=112500">BRACHYDACTYLY, TYPE A1; BDA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600726">INDIAN HEDGEHOG, DROSOPHILA, HOMOLOG OF; IHH</A><BR>
</TD>
</TR>
<TR><TD>IRS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:133974">GDB:133974</A></TD><TD>2q36-2q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147545">INSULIN RECEPTOR SUBSTRATE 1; IRS1</A><BR>
</TD>
</TR>
<TR><TD>ITGA6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128027">GDB:128027</A></TD><TD>2pter-2qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147556">INTEGRIN, ALPHA-6; ITGA6</A><BR>
</TD>
</TR>
<TR><TD>KHK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:391903">GDB:391903</A></TD><TD>2p23.3-2p23.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=229800">FRUCTOSURIA</A><BR>
</TD>
</TR>
<TR><TD>KYNU</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957925">GDB:9957925</A></TD><TD>2q22.2-2q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=236800"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605197"></A><BR>
</TD>
</TR>
<TR><TD>LCT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120140">GDB:120140</A></TD><TD>2q21-2q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=223000">DISACCHARIDE INTOLERANCE II</A><BR>
</TD>
</TR>
<TR><TD>LHCGR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125260">GDB:125260</A></TD><TD>2p21-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=152790">LUTEINIZING HORMONE/CHORIOGONADOTROPIN RECEPTOR; LHCGR</A><BR>
</TD>
</TR>
<TR><TD>LSFC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956219">GDB:9956219</A></TD><TD>2-2 2p16-2p16 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=220111">CYTOCHROME c OXIDASE DEFICIENCY, FRENCH-CANADIAN TYPE</A><BR>
</TD>
</TR>
<TR><TD>MSH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:203983">GDB:203983</A></TD><TD>2p16-2p16 2p22-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114500">CANCER OF COLON</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120435">COLON CANCER, FAMILIAL, NONPOLYPOSIS TYPE 1; FCC1</A><BR>
</TD>
</TR>
<TR><TD>MSH6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:632803">GDB:632803</A></TD><TD>2p16-2p16 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600678">G/T MISMATCH-BINDING PROTEIN; GTBP</A><BR>
</TD>
</TR>
<TR><TD>NEB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120224">GDB:120224</A></TD><TD>2q24.1-2q24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=161650">NEBULIN; NEB</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256030">NEMALINE MYOPATHY 2, AUTOSOMAL RECESSIVE; NEM2</A><BR>
</TD>
</TR>
<TR><TD>NMTC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498336">GDB:11498336</A></TD><TD>2q21-2q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188550">THYROID CARCINOMA, PAPILLARY</A><BR>
</TD>
</TR>
<TR><TD>NPHP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128050">GDB:128050</A></TD><TD>2q13-2q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256100">NEPHRONOPHTHISIS, FAMILIAL JUVENILE 1; NPHP1</A><BR>
</TD>
</TR>
<TR><TD>PAFAH1P1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:435099">GDB:435099</A></TD><TD>2p11.2-2p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601545">PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, GAMMA SUBUNIT</A><BR>
</TD>
</TR>
<TR><TD>PAX3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120495">GDB:120495</A></TD><TD>2q36-2q36 2q35-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148820">KLEIN-WAARDENBURG SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193500">WAARDENBURG SYNDROME; WS1</A><BR>
</TD>
</TR>
<TR><TD>PAX8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136447">GDB:136447</A></TD><TD>2q12-2q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167415">PAIRED BOX HOMEOTIC GENE 8; PAX8</A><BR>
</TD>
</TR>
<TR><TD>PMS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:386403">GDB:386403</A></TD><TD>2q31-2q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600258">POSTMEIOTIC SEGREGATION INCREASED (S. CEREVISIAE)-1; PMS1</A><BR>
</TD>
</TR>
<TR><TD>PNKD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5583973">GDB:5583973</A></TD><TD>2q33-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118800">CHOREOATHETOSIS, FAMILIAL PAROXYSMAL; FPD1</A><BR>
</TD>
</TR>
<TR><TD>PPH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1381541">GDB:1381541</A></TD><TD>2q31-2q32 2q33-2q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=178600">PULMONARY HYPERTENSION, PRIMARY; PPH1</A><BR>
</TD>
</TR>
<TR><TD>PROC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120317">GDB:120317</A></TD><TD>2q13-2q21 2q13-2q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176860">PROTEIN C DEFICIENCY, CONGENITAL THROMBOTIC DISEASE DUE TO</A><BR>
</TD>
</TR>
<TR><TD>REG1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132455">GDB:132455</A></TD><TD>2p12-2p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167770">REGENERATING ISLET-DERIVED 1-ALPHA; REG1A</A><BR>
</TD>
</TR>
<TR><TD>SAG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120365">GDB:120365</A></TD><TD>2q37.1-2q37.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181031">S-ANTIGEN; SAG</A><BR>
</TD>
</TR>
<TR><TD>SFTPB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120374">GDB:120374</A></TD><TD>2p12-2p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=178640">SURFACTANT-ASSOCIATED PROTEIN, PULMONARY-3; SFTP3</A><BR>
</TD>
</TR>
<TR><TD>SLC11A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:371444">GDB:371444</A></TD><TD>2q35-2q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109720">CIRRHOSIS, PRIMARY; PBC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600266">NATURAL RESISTANCE-ASSOCIATED MACROPHAGE PROTEIN 1; NRAMP1</A><BR>
</TD>
</TR>
<TR><TD>SLC3A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:202968">GDB:202968</A></TD><TD>2p16.3-2p16.3 2p21-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104614">SOLUTE CARRIER FAMILY 3, MEMBER 1; SLC3A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=220100">CYSTINURIA; CSNU</A><BR>
</TD>
</TR>
<TR><TD>SOS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230004">GDB:230004</A></TD><TD>2p22-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=135300">GINGIVAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182530">SON OF SEVENLESS (DROSOPHILA) HOMOLOG 1; SOS1</A><BR>
</TD>
</TR>
<TR><TD>SPG4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230127">GDB:230127</A></TD><TD>2p24-2p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182601">SPASTIC PARAPLEGIA-4, AUTOSOMAL DOMINANT; SPG4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604277"></A><BR>
</TD>
</TR>
<TR><TD>SRD5A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127343">GDB:127343</A></TD><TD>2p23-2p23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264600">PSEUDOVAGINAL PERINEOSCROTAL HYPOSPADIAS; PPSH</A><BR>
</TD>
</TR>
<TR><TD>TCL4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136378">GDB:136378</A></TD><TD>2q34-2q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186860">T-CELL LEUKEMIA/LYMPHOMA-4; TCL4</A><BR>
</TD>
</TR>
<TR><TD>TGFA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120435">GDB:120435</A></TD><TD>2p13-2p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190170">TRANSFORMING GROWTH FACTOR, ALPHA; TGFA</A><BR>
</TD>
</TR>
<TR><TD>TMD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9837196">GDB:9837196</A></TD><TD>2q31-2q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600334">TIBIAL MUSCULAR DYSTROPHY, TARDIVE</A><BR>
</TD>
</TR>
<TR><TD>TPO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120446">GDB:120446</A></TD><TD>2p25-2p25 2p25-2p24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=274500">THYROID HORMONOGENESIS, GENETIC DEFECT IN, IIA</A><BR>
</TD>
</TR>
<TR><TD>UGT1A@</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120007">GDB:120007</A></TD><TD>2q37-2q37 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191740">UDP GLUCURONOSYLTRANSFERASE 1 FAMILY, A1; UGT1A1</A><BR>
</TD>
</TR>
<TR><TD>UV24</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955737">GDB:9955737</A></TD><TD>2pter-2qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=192070">UV-DAMAGE, EXCISION REPAIR OF, UV-24</A><BR>
</TD>
</TR>
<TR><TD>WSS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955707">GDB:9955707</A></TD><TD>2q32-2q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278250">WRINKLY SKIN SYNDROME; WSS</A><BR>
</TD>
</TR>
<TR><TD>XDH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:266386">GDB:266386</A></TD><TD>2p23-2p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278300">XANTHINURIA</A><BR>
</TD>
</TR>
<TR><TD>ZAP70</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433738">GDB:433738</A></TD><TD>2q11-2q13 2q12-2q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176947">SYK-RELATED TYROSINE KINASE; SRK</A><BR>
</TD>
</TR>
<TR><TD>ZFHX1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958310">GDB:9958310</A></TD><TD>2q22-2q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=235730">DISEASE, MICROCEPHALY, AND IRIS COLOBOMA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605802"></A><BR>
</TD>
</TR>
<TR><TD>ACAA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119643">GDB:119643</A></TD><TD>3p23-3p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261510">PEROXISOMAL 3-OXOACYL-COENZYME A THIOLASE DEFICIENCY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604054"></A><BR>
</TD>
</TR>
<TR><TD>AGS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10795417">GDB:10795417</A></TD><TD>3p21-3p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=225750">ENCEPHALOPATHY, FAMILIAL INFANTILE, WITH CALCIFICATION OF BASAL GANGLIA</A><BR>
</TD>
</TR>
<TR><TD>AGTR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132359">GDB:132359</A></TD><TD>3q21-3q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106165">ANGIOTENSIN II RECEPTOR, VASCULAR TYPE 1; AT2R1</A><BR>
</TD>
</TR>
<TR><TD>AHSG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118985">GDB:118985</A></TD><TD>3q27-3q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138680">ALPHA-2-HS-GLYCOPROTEIN; AHSG</A><BR>
</TD>
</TR>
<TR><TD>AMT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132138">GDB:132138</A></TD><TD>3p21.3-3p21.2 3p21.2-3p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238310">HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE II; NKH2</A><BR>
</TD>
</TR>
<TR><TD>ARMET</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9959049">GDB:9959049</A></TD><TD>3p21.1-3p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601916">ARGININE-RICH PROTEIN</A><BR>
</TD>
</TR>
<TR><TD>BBS3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:376501">GDB:376501</A></TD><TD>3p-3p 3p12.3-3q11.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600151">BARDET-BIEDL SYNDROME, TYPE 3; BBS3</A><BR>
</TD>
</TR>
<TR><TD>BCHE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120558">GDB:120558</A></TD><TD>3q26.1-3q26.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177400">BUTYRYLCHOLINESTERASE; BCHE</A><BR>
</TD>
</TR>
<TR><TD>BCPM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433809">GDB:433809</A></TD><TD>3q21-3q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=169600">BENIGN CHRONIC PEMPHIGUS; BCPM</A><BR>
</TD>
</TR>
<TR><TD>BTD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:309078">GDB:309078</A></TD><TD>3p25-3p25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253260">BIOTINIDASE; BTD</A><BR>
</TD>
</TR>
<TR><TD>CASR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134196">GDB:134196</A></TD><TD>3q21-3q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145980">HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL; HHC1</A><BR>
</TD>
</TR>
<TR><TD>CCR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:337364">GDB:337364</A></TD><TD>3p21-3p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601267">CHEMOKINE (C-C) RECEPTOR 2; CMKBR2</A><BR>
</TD>
</TR>
<TR><TD>CCR5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1230510">GDB:1230510</A></TD><TD>3p21-3p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601373">CHEMOKINE (C-C) RECEPTOR 5; CMKBR5</A><BR>
</TD>
</TR>
<TR><TD>CDL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136344">GDB:136344</A></TD><TD>3q26.3-3q26.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122470">DE LANGE SYNDROME; CDL</A><BR>
</TD>
</TR>
<TR><TD>CMT2B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:604021">GDB:604021</A></TD><TD>3q13-3q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600882">CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, B; CMT2B</A><BR>
</TD>
</TR>
<TR><TD>COL7A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128750">GDB:128750</A></TD><TD>3p21-3p21 3p21.3-3p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120120">COLLAGEN, TYPE VII, ALPHA-1; COL7A1</A><BR>
</TD>
</TR>
<TR><TD>CP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119069">GDB:119069</A></TD><TD>3q23-3q25 3q21-3q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=117700">CERULOPLASMIN; CP</A><BR>
</TD>
</TR>
<TR><TD>CPO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119070">GDB:119070</A></TD><TD>3q12-3q12 9pter-9qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121300">COPROPORPHYRIA</A><BR>
</TD>
</TR>
<TR><TD>CRV</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498333">GDB:11498333</A></TD><TD>3p21.3-3p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=192315">VASCULOPATHY, RETINAL, WITH CEREBRAL LEUKODYSTROPHY</A><BR>
</TD>
</TR>
<TR><TD>CTNNB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:141922">GDB:141922</A></TD><TD>3p22-3p22 3p21.3-3p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114550">CANCER, HEPATOCELLULAR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=116806">CATENIN, BETA 1; CTNNB1</A><BR>
</TD>
</TR>
<TR><TD>DEM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:681157">GDB:681157</A></TD><TD>3p12-3q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600795">DEMENTIA, FAMILIAL NONSPECIFIC; DEM</A><BR>
</TD>
</TR>
<TR><TD>ETM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9732523">GDB:9732523</A></TD><TD>3q13-3q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190300">TREMOR, HEREDITARY ESSENTIAL 1; ETM1</A><BR>
</TD>
</TR>
<TR><TD>FANCD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:698345">GDB:698345</A></TD><TD>3p25.3-3p25.3 3pter-3p24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227646">FANCONI PANCYTOPENIA, COMPLEMENTATION GROUP D</A><BR>
</TD>
</TR>
<TR><TD>FIH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955790">GDB:9955790</A></TD><TD>3q13-3q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146200">HYPOPARATHYROIDISM, FAMILIAL ISOLATED; FIH</A><BR>
</TD>
</TR>
<TR><TD>FOXL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129025">GDB:129025</A></TD><TD>3q23-3q23 3q22-3q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=110100">BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS; BPES</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605597"></A><BR>
</TD>
</TR>
<TR><TD>GBE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138442">GDB:138442</A></TD><TD>3p12-3p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232500">GLYCOGEN STORAGE DISEASE IV</A><BR>
</TD>
</TR>
<TR><TD>GLB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119987">GDB:119987</A></TD><TD>3p22-3p21.33 3p21.33-3p21.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230500">GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I</A><BR>
</TD>
</TR>
<TR><TD>GLC1C</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3801941">GDB:3801941</A></TD><TD>3q21-3q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601682">GLAUCOMA 1, OPEN ANGLE, C; GLC1C</A><BR>
</TD>
</TR>
<TR><TD>GNAI2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120516">GDB:120516</A></TD><TD>3p21.3-3p21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139360">GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING, POLYPEPTIDE-2;</A><BR>
</TD>
</TR>
<TR><TD>GNAT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119277">GDB:119277</A></TD><TD>3p21.3-3p21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139330">GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-TRANSDUCING, POLYPEPTIDE</A><BR>
</TD>
</TR>
<TR><TD>GP9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126370">GDB:126370</A></TD><TD>3pter-3qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173515">PLATELET GLYCOPROTEIN IX; GP9</A><BR>
</TD>
</TR>
<TR><TD>GPX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119282">GDB:119282</A></TD><TD>3q11-3q12 3p21.3-3p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138320">GLUTATHIONE PEROXIDASE; GPX1</A><BR>
</TD>
</TR>
<TR><TD>HGD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:203935">GDB:203935</A></TD><TD>3q21-3q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203500">ALKAPTONURIA; AKU</A><BR>
</TD>
</TR>
<TR><TD>HRG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120055">GDB:120055</A></TD><TD>3q27-3q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142640">HISTIDINE-RICH GLYCOPROTEIN; HRG; HRGP</A><BR>
</TD>
</TR>
<TR><TD>ITIH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120107">GDB:120107</A></TD><TD>3p21.2-3p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147270">INTER-ALPHA-TRYPSIN INHIBITOR, HEAVY CHAIN-1; ITIH1; IATIH; ITIH</A><BR>
</TD>
</TR>
<TR><TD>KNG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125256">GDB:125256</A></TD><TD>3q27-3q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=228960">FLAUJEAC FACTOR DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>LPP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1391795">GDB:1391795</A></TD><TD>3q27-3q28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600700">LIM DOMAIN-CONTAINING PREFERRED TRANSLOCATION PARTNER IN LIPOMA; LPP</A><BR>
</TD>
</TR>
<TR><TD>LRS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:682448">GDB:682448</A></TD><TD>3p21.1-3p14.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150250">LARSEN SYNDROME, AUTOSOMAL DOMINANT; LRS1</A><BR>
</TD>
</TR>
<TR><TD>MCCC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135989">GDB:135989</A></TD><TD>3q27-3q27 3q25-3q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=210200">BETA-METHYLCROTONYLGLYCINURIA I</A><BR>
</TD>
</TR>
<TR><TD>MDS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250411">GDB:250411</A></TD><TD>3q26-3q26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600049">MYELODYSPLASIA SYNDROME 1; MDS1</A><BR>
</TD>
</TR>
<TR><TD>MHS4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:574245">GDB:574245</A></TD><TD>3q13.1-3q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600467">HYPERTHERMIA SUSCEPTIBILITY-4; MHS4</A><BR>
</TD>
</TR>
<TR><TD>MITF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:214776">GDB:214776</A></TD><TD>3p14.1-3p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156845">MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193510">WAARDENBURG SYNDROME, TYPE II; WS2</A><BR>
</TD>
</TR>
<TR><TD>MLH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:249617">GDB:249617</A></TD><TD>3p23-3p22 3p21.3-3p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120436">COLON CANCER, FAMILIAL, NONPOLYPOSIS TYPE 2; FCC2</A><BR>
</TD>
</TR>
<TR><TD>MYL3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120218">GDB:120218</A></TD><TD>3p21.3-3p21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160790">MYOSIN, LIGHT CHAIN, ALKALI, VENTRICULAR AND SKELETAL SLOW; MYL3</A><BR>
</TD>
</TR>
<TR><TD>MYMY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11500610">GDB:11500610</A></TD><TD>3p26-3p24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252350">DISEASE</A><BR>
</TD>
</TR>
<TR><TD>OPA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118848">GDB:118848</A></TD><TD>3q28-3q29 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=165500">OPTIC ATROPHY 1; OPA1</A><BR>
</TD>
</TR>
<TR><TD>P2RY12</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11513875">GDB:11513875</A></TD><TD>3q24-3q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600515">ADP-RECEPTOR DEFECT</A><BR>
</TD>
</TR>
<TR><TD>PBXP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125352">GDB:125352</A></TD><TD>3q22-3q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176310">PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR-1; PBX1</A><BR>
</TD>
</TR>
<TR><TD>PCCB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119474">GDB:119474</A></TD><TD>3q21-3q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232050">GLYCINEMIA, KETOTIC, II</A><BR>
</TD>
</TR>
<TR><TD>POU1F1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129070">GDB:129070</A></TD><TD>3p11-3p11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173110">POU DOMAIN, CLASS 1, TRANSCRIPTION FACTOR 1; POU1F1</A><BR>
</TD>
</TR>
<TR><TD>PPARG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1223810">GDB:1223810</A></TD><TD>3p25-3p25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114500">CANCER OF COLON</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601487">PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR, GAMMA; PPARG</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604367"></A><BR>
</TD>
</TR>
<TR><TD>PROS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120721">GDB:120721</A></TD><TD>3p11-3q11 3p11.1-3q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176880">PROTEIN S, ALPHA; PROS1</A><BR>
</TD>
</TR>
<TR><TD>PTHR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138128">GDB:138128</A></TD><TD>3p22-3p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156400">METAPHYSEAL CHONDRODYSPLASIA, MURK JANSEN TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168468">PARATHYROID HORMONE RECEPTOR 1; PTHR1</A><BR>
</TD>
</TR>
<TR><TD>RCA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230233">GDB:230233</A></TD><TD>3p14.2-3p14.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=144700">RENAL CARCINOMA, FAMILIAL, ASSOCIATED 1; RCA1</A><BR>
</TD>
</TR>
<TR><TD>RHO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120347">GDB:120347</A></TD><TD>3q21.3-3q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180380">RHODOPSIN; RHO</A><BR>
</TD>
</TR>
<TR><TD>SCA7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:454471">GDB:454471</A></TD><TD>3p21.1-3p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164500">SPINOCEREBELLAR ATAXIA 7; SCA7</A><BR>
</TD>
</TR>
<TR><TD>SCLC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955750">GDB:9955750</A></TD><TD>3p23-3p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182280">SMALL-CELL CANCER OF THE LUNG; SCCL</A><BR>
</TD>
</TR>
<TR><TD>SCN5A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132152">GDB:132152</A></TD><TD>3p21-3p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600163">SODIUM CHANNEL, VOLTAGE-GATED, TYPE V, ALPHA POLYPEPTIDE; SCN5A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603830"></A><BR>
</TD>
</TR>
<TR><TD>SI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120377">GDB:120377</A></TD><TD>3q25.2-3q26.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222900">DISACCHARIDE INTOLERANCE I</A><BR>
</TD>
</TR>
<TR><TD>SLC25A20</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6503297">GDB:6503297</A></TD><TD>3p21.31-3p21.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212138">CARNITINE-ACYLCARNITINE TRANSLOCASE; CACT</A><BR>
</TD>
</TR>
<TR><TD>SLC2A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119995">GDB:119995</A></TD><TD>3q26.2-3q27 3q26.1-3q26.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138160">SOLUTE CARRIER FAMILY 2, MEMBER 2; SLC2A2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227810">FANCONI-BICKEL SYNDROME; FBS</A><BR>
</TD>
</TR>
<TR><TD>TF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120432">GDB:120432</A></TD><TD>3q21-3q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190000">TRANSFERRIN; TF</A><BR>
</TD>
</TR>
<TR><TD>TGFBR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:224909">GDB:224909</A></TD><TD>3p22-3p22 3pter-3p24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190182">TRANSFORMING GROWTH FACTOR-BETA RECEPTOR, TYPE II; TGFBR2</A><BR>
</TD>
</TR>
<TR><TD>THPO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:374007">GDB:374007</A></TD><TD>3q26.3-3q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600044">THROMBOPOIETIN; THPO</A><BR>
</TD>
</TR>
<TR><TD>THRB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120731">GDB:120731</A></TD><TD>3p24.1-3p22 3p24.3-3p24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190160">THYROID HORMONE RECEPTOR, BETA; THRB</A><BR>
</TD>
</TR>
<TR><TD>TKT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132402">GDB:132402</A></TD><TD>3p14.3-3p14.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277730">WERNICKE-KORSAKOFF SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>TM4SF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250815">GDB:250815</A></TD><TD>3q21-3q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191155">TUMOR-ASSOCIATED ANTIGEN L6; TAAL6</A><BR>
</TD>
</TR>
<TR><TD>TRH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128072">GDB:128072</A></TD><TD>3pter-3qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=275120">THYROTROPIN-RELEASING HORMONE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>UMPS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120482">GDB:120482</A></TD><TD>3q13-3q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=258900">OROTICACIDURIA I</A><BR>
</TD>
</TR>
<TR><TD>UQCRC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:141850">GDB:141850</A></TD><TD>3p21.3-3p21.2 3p21.3-3p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191328">UBIQUINOL-CYTOCHROME c REDUCTASE CORE PROTEIN I; UQCRC1</A><BR>
</TD>
</TR>
<TR><TD>USH3A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:392645">GDB:392645</A></TD><TD>3q21-3q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276902">USHER SYNDROME, TYPE III; USH3</A><BR>
</TD>
</TR>
<TR><TD>VHL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120488">GDB:120488</A></TD><TD>3p26-3p25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193300">VON HIPPEL-LINDAU SYNDROME; VHL</A><BR>
</TD>
</TR>
<TR><TD>WS2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128053">GDB:128053</A></TD><TD>3p14.2-3p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156845">MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193510">WAARDENBURG SYNDROME, TYPE II; WS2</A><BR>
</TD>
</TR>
<TR><TD>XPC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134769">GDB:134769</A></TD><TD>3p25.1-3p25.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278720">XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC</A><BR>
</TD>
</TR>
<TR><TD>ZNF35</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120507">GDB:120507</A></TD><TD>3p21-3p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194533">ZINC FINGER PROTEIN-35; ZNF35</A><BR>
</TD>
</TR>
<TR><TD>ADH1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119651">GDB:119651</A></TD><TD>4q21-4q23 4q22-4q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103720">ALCOHOL DEHYDROGENASE-2; ADH2</A><BR>
</TD>
</TR>
<TR><TD>ADH1C</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119652">GDB:119652</A></TD><TD>4q21-4q23 4q22-4q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103730">ALCOHOL DEHYDROGENASE-3; ADH3</A><BR>
</TD>
</TR>
<TR><TD>AFP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119660">GDB:119660</A></TD><TD>4q11-4q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104150">ALPHA-FETOPROTEIN; AFP</A><BR>
</TD>
</TR>
<TR><TD>AGA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118981">GDB:118981</A></TD><TD>4q23-4q35 4q32-4q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=208400">ASPARTYLGLUCOSAMINURIA; AGU</A><BR>
</TD>
</TR>
<TR><TD>AIH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118751">GDB:118751</A></TD><TD>4q11-4q13 4q13.3-4q21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104500">AMELOGENESIS IMPERFECTA 2, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT;</A><BR>
</TD>
</TR>
<TR><TD>ALB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118990">GDB:118990</A></TD><TD>4q11-4q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103600">ALBUMIN; ALB</A><BR>
</TD>
</TR>
<TR><TD>ASMD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119705">GDB:119705</A></TD><TD>4q-4q 4q28-4q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107250">ANTERIOR SEGMENT OCULAR DYSGENESIS; ASOD</A><BR>
</TD>
</TR>
<TR><TD>BFHD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498907">GDB:11498907</A></TD><TD>4q34.1-4q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142669">DYSPLASIA, BEUKES TYPE</A><BR>
</TD>
</TR>
<TR><TD>CNGA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127557">GDB:127557</A></TD><TD>4p14-4q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123825">CYCLIC NUCLEOTIDE GATED CHANNEL, PHOTORECEPTOR, cGMP GATED, 1; CNCG1</A><BR>
</TD>
</TR>
<TR><TD>CRBM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958132">GDB:9958132</A></TD><TD>4p16.3-4p16.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118400">CHERUBISM</A><BR>
</TD>
</TR>
<TR><TD>DCK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126810">GDB:126810</A></TD><TD>4q13.3-4q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125450">DEOXYCYTIDINE KINASE; DCK</A><BR>
</TD>
</TR>
<TR><TD>DSPP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5560457">GDB:5560457</A></TD><TD>4pter-4qter 4q21.3-4q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125485">DENTIN PHOSPHOPROTEIN; DPP</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125490">DENTINOGENESIS IMPERFECTA; DGI1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605594"></A><BR>
</TD>
</TR>
<TR><TD>DTDP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955810">GDB:9955810</A></TD><TD>4q-4q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125420">DENTIN DYSPLASIA, TYPE II</A><BR>
</TD>
</TR>
<TR><TD>ELONG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498700">GDB:11498700</A></TD><TD>4q24-4q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=152430"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606460"></A><BR>
</TD>
</TR>
<TR><TD>ENAM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955259">GDB:9955259</A></TD><TD>4q21-4q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104500">AMELOGENESIS IMPERFECTA 2, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT;</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104530">AMELOGENESIS IMPERFECTA, HYPOPLASTIC TYPE</A><BR>
</TD>
</TR>
<TR><TD>ETFDH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135992">GDB:135992</A></TD><TD>4q32-4q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231675">GLUTARICACIDURIA IIC; GA IIC</A><BR>
</TD>
</TR>
<TR><TD>EVC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:555573">GDB:555573</A></TD><TD>4p16-4p16 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=225500">ELLIS-VAN CREVELD SYNDROME; EVC</A><BR>
</TD>
</TR>
<TR><TD>F11</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119891">GDB:119891</A></TD><TD>4q35-4q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264900">PTA DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>FABP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119127">GDB:119127</A></TD><TD>4q28-4q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134640">FATTY ACID BINDING PROTEIN 2, INTESTINAL; FABP2</A><BR>
</TD>
</TR>
<TR><TD>FGA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119129">GDB:119129</A></TD><TD>4q28-4q28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105200">AMYLOIDOSIS, FAMILIAL VISCERAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134820">FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA</A><BR>
</TD>
</TR>
<TR><TD>FGB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119130">GDB:119130</A></TD><TD>4q28-4q28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134830">FIBRINOGEN, B BETA POLYPEPTIDE; FGB</A><BR>
</TD>
</TR>
<TR><TD>FGFR3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127526">GDB:127526</A></TD><TD>4p16.3-4p16.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100800">ACHONDROPLASIA; ACH</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109800">BLADDER CANCER</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134934">FIBROBLAST GROWTH FACTOR RECEPTOR-3; FGFR3</A><BR>
</TD>
</TR>
<TR><TD>FGG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119132">GDB:119132</A></TD><TD>4q28-4q28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134850">FIBRINOGEN, G GAMMA POLYPEPTIDE; FGG</A><BR>
</TD>
</TR>
<TR><TD>FSHMD1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119914">GDB:119914</A></TD><TD>4q35-4q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158900">FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A</A><BR>
</TD>
</TR>
<TR><TD>GC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119263">GDB:119263</A></TD><TD>4q12-4q13 4q12-4q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139200">GROUP-SPECIFIC COMPONENT; GC</A><BR>
</TD>
</TR>
<TR><TD>GNPTA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119280">GDB:119280</A></TD><TD>4q21-4q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252500">MUCOLIPIDOSIS II; ML2; ML II</A><BR>
</TD>
</TR>
<TR><TD>GNRHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136456">GDB:136456</A></TD><TD>4q13-4q13 4q21.2-4q21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138850">GONADOTROPIN-RELEASING HORMONE RECEPTOR; GNRHR</A><BR>
</TD>
</TR>
<TR><TD>GYPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118890">GDB:118890</A></TD><TD>4q28-4q31 4q28.2-4q31.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=111300">BLOOD GROUP--MN LOCUS; MN</A><BR>
</TD>
</TR>
<TR><TD>HCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954675">GDB:9954675</A></TD><TD>4q33-4qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143870">HYPERCALCIURIA, FAMILIAL IDIOPATHIC</A><BR>
</TD>
</TR>
<TR><TD>HCL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119305">GDB:119305</A></TD><TD>4q28-4q31 4q-4q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266300">HAIR COLOR-2; HCL2</A><BR>
</TD>
</TR>
<TR><TD>HD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119307">GDB:119307</A></TD><TD>4p16.3-4p16.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143100">HUNTINGTON DISEASE; HD</A><BR>
</TD>
</TR>
<TR><TD>HTN3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125601">GDB:125601</A></TD><TD>4q12-4q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142702">HISTATIN-3; HTN3</A><BR>
</TD>
</TR>
<TR><TD>HVBS6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120687">GDB:120687</A></TD><TD>4q32-4q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142380">HEPATOCELLULAR CARCINOMA-2; HCC2</A><BR>
</TD>
</TR>
<TR><TD>IDUA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119327">GDB:119327</A></TD><TD>4p16.3-4p16.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252800">MUCOPOLYSACCHARIDOSIS TYPE I; MPS I</A><BR>
</TD>
</TR>
<TR><TD>IF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120077">GDB:120077</A></TD><TD>4q24-4q25 4q25-4q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217030">COMPLEMENT COMPONENT-3 INACTIVATOR, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>JPD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120113">GDB:120113</A></TD><TD>4pter-4qter 4q12-4q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170650">PERIODONTITIS, JUVENILE; JPD</A><BR>
</TD>
</TR>
<TR><TD>KIT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120117">GDB:120117</A></TD><TD>4q12-4q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164920">V-KIT HARDY-ZUCKERMAN 4 FELINE SARCOMA VIRAL ONCOGENE HOMOLOG; KIT</A><BR>
</TD>
</TR>
<TR><TD>KLKB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127575">GDB:127575</A></TD><TD>4q34-4q35 4q35-4q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=229000">FLETCHER FACTOR DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>LQT4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:682072">GDB:682072</A></TD><TD>4q25-4q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600919">SYNDROME WITHOUT PSYCHOMOTOR RETARDATION</A><BR>
</TD>
</TR>
<TR><TD>MANBA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125261">GDB:125261</A></TD><TD>4q21-4q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248510">MANNOSIDOSIS, BETA; MANB1</A><BR>
</TD>
</TR>
<TR><TD>MLLT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136792">GDB:136792</A></TD><TD>4q21-4q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159557">MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 2; MLLT2</A><BR>
</TD>
</TR>
<TR><TD>MSX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120683">GDB:120683</A></TD><TD>4p16.3-4p16.1 4p16.1-4p16.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142983">MSH, DROSOPHILA, HOMEO BOX, HOMOLOG OF, 1; MSX1</A><BR>
</TD>
</TR>
<TR><TD>MTP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:228961">GDB:228961</A></TD><TD>4q24-4q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157147">MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN, 88 KD; MTP</A><BR>
</TD>
</TR>
<TR><TD>NR3C2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120188">GDB:120188</A></TD><TD>4q31-4q31 4q31.1-4q31.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264350">PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1</A><BR>
</TD>
</TR>
<TR><TD>PBT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120260">GDB:120260</A></TD><TD>4q12-4q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172800">PIEBALD TRAIT; PBT</A><BR>
</TD>
</TR>
<TR><TD>PDE6B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125915">GDB:125915</A></TD><TD>4p16.3-4p16.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=163500">NIGHTBLINDNESS, CONGENITAL STATIONARY; CSNB3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180072">PHOSPHODIESTERASE 6B, cGMP-SPECIFIC, ROD, BETA; PDE6B</A><BR>
</TD>
</TR>
<TR><TD>PEE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:7016765">GDB:7016765</A></TD><TD>4q31-4q34 4q25-4qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=189800">1; PEE1</A><BR>
</TD>
</TR>
<TR><TD>PITX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134770">GDB:134770</A></TD><TD>4q25-4q27 4q25-4q26 4q25-4q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137600">IRIDOGONIODYSGENESIS, TYPE 2; IRID2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180500">RIEGER SYNDROME, TYPE 1; RIEG1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601542">RIEG BICOID-RELATED HOMEOBOX TRANSCRIPTION FACTOR 1; RIEG1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601765">HOMEO BOX 2</A><BR>
</TD>
</TR>
<TR><TD>PKD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118851">GDB:118851</A></TD><TD>4q21-4q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173910">POLYCYSTIC KIDNEY DISEASE 2; PKD2</A><BR>
</TD>
</TR>
<TR><TD>QDPR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120331">GDB:120331</A></TD><TD>4p15.3-4p15.3 4p15.31-4p15.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261630">PHENYLKETONURIA II</A><BR>
</TD>
</TR>
<TR><TD>SGCB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:702072">GDB:702072</A></TD><TD>4q12-4q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600900">MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E</A><BR>
</TD>
</TR>
<TR><TD>SLC25A4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119680">GDB:119680</A></TD><TD>4q35-4q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103220">ADENINE NUCLEOTIDE TRANSLOCATOR 1; ANT1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157640">PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; PEO</A><BR>
</TD>
</TR>
<TR><TD>SNCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439047">GDB:439047</A></TD><TD>4q21.3-4q22 4q21-4q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=163890">SYNUCLEIN, ALPHA; SNCA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601508">PARKINSON DISEASE, FAMILIAL, TYPE 1; PARK1</A><BR>
</TD>
</TR>
<TR><TD>SOD3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125291">GDB:125291</A></TD><TD>4p16.3-4q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=185490">SUPEROXIDE DISMUTASE, EXTRACELLULAR; SOD3</A><BR>
</TD>
</TR>
<TR><TD>STATH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120391">GDB:120391</A></TD><TD>4q11-4q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=184470">STATHERIN; STATH; STR</A><BR>
</TD>
</TR>
<TR><TD>TAPVR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:392646">GDB:392646</A></TD><TD>4p13-4q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106700">ANOMALOUS PULMONARY VENOUS RETURN; APVR</A><BR>
</TD>
</TR>
<TR><TD>TYS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119624">GDB:119624</A></TD><TD>4q-4q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181600">SCLEROTYLOSIS; TYS</A><BR>
</TD>
</TR>
<TR><TD>WBS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132426">GDB:132426</A></TD><TD>4q33-4q35.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194050">WILLIAMS-BEUREN SYNDROME; WBS</A><BR>
</TD>
</TR>
<TR><TD>WFS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:434294">GDB:434294</A></TD><TD>4p-4p 4p16-4p16 4p16.1-4p16.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222300">DIABETES MELLITUS AND INSIPIDUS WITH OPTIC ATROPHY AND DEAFNESS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600965">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 6; DFNA6</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605957"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606201"></A><BR>
</TD>
</TR>
<TR><TD>WHCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125355">GDB:125355</A></TD><TD>4p16.3-4p16.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194190">WOLF-HIRSCHHORN SYNDROME; WHS</A><BR>
</TD>
</TR>
<TR><TD>ADAMTS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957209">GDB:9957209</A></TD><TD>5q23-5q34 5q35.3-5q35.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=225410">EHLERS-DANLOS SYNDROME, TYPE VII, AUTOSOMAL RECESSIVE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604539"></A><BR>
</TD>
</TR>
<TR><TD>ADRB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120541">GDB:120541</A></TD><TD>5q31-5q32 5q32-5q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109690">BETA-2-ADRENERGIC RECEPTOR; ADRB2</A><BR>
</TD>
</TR>
<TR><TD>AMCN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9836823">GDB:9836823</A></TD><TD>5q35-5q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=208100">ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE</A><BR>
</TD>
</TR>
<TR><TD>AP3B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955590">GDB:9955590</A></TD><TD>5q12.1-5q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203300">HERMANSKY-PUDLAK SYNDROME; HPS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603401"></A><BR>
</TD>
</TR>
<TR><TD>APC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119682">GDB:119682</A></TD><TD>5q21-5q22 5q22.1-5q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=175100">ADENOMATOUS POLYPOSIS OF THE COLON; APC</A><BR>
</TD>
</TR>
<TR><TD>ARSB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119008">GDB:119008</A></TD><TD>5p11-5q13 5q11-5q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253200">MUCOPOLYSACCHARIDOSIS TYPE VI; MPS VI</A><BR>
</TD>
</TR>
<TR><TD>B4GALT7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957653">GDB:9957653</A></TD><TD>5q35.2-5q35.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130070">SYNDROME, PROGEROID FORM</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604327"></A><BR>
</TD>
</TR>
<TR><TD>BHR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956078">GDB:9956078</A></TD><TD>5q31-5q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600807">ASTHMA</A><BR>
</TD>
</TR>
<TR><TD>C6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119045">GDB:119045</A></TD><TD>5p14-5p12 5p13-5p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217050">COMPLEMENT COMPONENT-6, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>C7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119046">GDB:119046</A></TD><TD>5p14-5p12 5p13-5p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217070">COMPLEMENT COMPONENT-7, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>CCAL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5584265">GDB:5584265</A></TD><TD>5p15.2-5p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118600">CHONDROCALCINOSIS, FAMILIAL ARTICULAR</A><BR>
</TD>
</TR>
<TR><TD>CKN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128586">GDB:128586</A></TD><TD>5pter-5qter 5q12.1-5q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=216400">COCKAYNE SYNDROME, TYPE I; CKN1</A><BR>
</TD>
</TR>
<TR><TD>CMDJ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9595425">GDB:9595425</A></TD><TD>5p15.2-5p14.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123000">CRANIOMETAPHYSEAL DYSPLASIA, JACKSON TYPE; CMDJ</A><BR>
</TD>
</TR>
<TR><TD>CRHBP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127438">GDB:127438</A></TD><TD>5q-5q 5q12-5q13.3 5q12-5q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122559">CORTICOTROPIN RELEASING HORMONE-BINDING PROTEIN; CRHBP</A><BR>
</TD>
</TR>
<TR><TD>CSF1R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120600">GDB:120600</A></TD><TD>5q33.3-5q34 5q33.2-5q33.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164770">COLONY-STIMULATING FACTOR-1 RECEPTOR; CSF1R</A><BR>
</TD>
</TR>
<TR><TD>DHFR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119845">GDB:119845</A></TD><TD>5q11.2-5q13.2 5q12-5q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126060">DIHYDROFOLATE REDUCTASE; DHFR</A><BR>
</TD>
</TR>
<TR><TD>DIAPH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9835482">GDB:9835482</A></TD><TD>5q31-5q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=124900">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 1; DFNA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602121">DIAPHANOUS, DROSOPHILA, HOMOLOG OF, 1</A><BR>
</TD>
</TR>
<TR><TD>DTR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119853">GDB:119853</A></TD><TD>5q23-5q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126150">DIPHTHERIA TOXIN SENSITIVITY; DTS</A><BR>
</TD>
</TR>
<TR><TD>EOS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956083">GDB:9956083</A></TD><TD>5q31-5q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131400">EOSINOPHILIA, FAMILIAL</A><BR>
</TD>
</TR>
<TR><TD>EPD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11509746">GDB:11509746</A></TD><TD>5q31.2-5q31.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266100">PYRIDOXINE DEPENDENCY WITH SEIZURES</A><BR>
</TD>
</TR>
<TR><TD>ERVR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9835857">GDB:9835857</A></TD><TD>5q13-5q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143200">HYALOIDEORETINAL DEGENERATION OF WAGNER</A><BR>
</TD>
</TR>
<TR><TD>F12</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119892">GDB:119892</A></TD><TD>5q33-5qter 5q34-5qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=234000">HAGEMAN FACTOR DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>FBN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128122">GDB:128122</A></TD><TD>5q21-5q33 5q23-5q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121050">CONTRACTURAL ARACHNODACTYLY, CONGENITAL; CCA</A><BR>
</TD>
</TR>
<TR><TD>GDNF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:450609">GDB:450609</A></TD><TD>5p13.3-5p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600837">GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; GDNF</A><BR>
</TD>
</TR>
<TR><TD>GHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119984">GDB:119984</A></TD><TD>5p14-5p12 5p13-5p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600946">GROWTH HORMONE RECEPTOR; GHR</A><BR>
</TD>
</TR>
<TR><TD>GLRA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118801">GDB:118801</A></TD><TD>5q32-5q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138491">GLYCINE RECEPTOR, ALPHA-1 SUBUNIT; GLRA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=149400">KOK DISEASE</A><BR>
</TD>
</TR>
<TR><TD>GM2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120000">GDB:120000</A></TD><TD>5q32-5q33 5q31.3-5q33.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=272750">TAY-SACHS DISEASE, AB VARIANT</A><BR>
</TD>
</TR>
<TR><TD>HEXB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119308">GDB:119308</A></TD><TD>5q13-5q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=268800">SANDHOFF DISEASE</A><BR>
</TD>
</TR>
<TR><TD>HSD17B4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:385059">GDB:385059</A></TD><TD>5q2-5q2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601860">17-@BETA-HYDROXYSTEROID DEHYDROGENASE IV; HSD17B4</A><BR>
</TD>
</TR>
<TR><TD>ITGA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128031">GDB:128031</A></TD><TD>5q23-5q31 5q11.1-5q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=192974">INTEGRIN, ALPHA-2; ITGA2</A><BR>
</TD>
</TR>
<TR><TD>KFS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958987">GDB:9958987</A></TD><TD>5q11.2-5q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214300">VERTEBRAL FUSION</A><BR>
</TD>
</TR>
<TR><TD>LGMD1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118832">GDB:118832</A></TD><TD>5q22-5q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159000">MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1A; LGMD1A</A><BR>
</TD>
</TR>
<TR><TD>LOX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119367">GDB:119367</A></TD><TD>5q23.3-5q31.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153455">LYSYL OXIDASE; LOX</A><BR>
</TD>
</TR>
<TR><TD>LTC4S</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:384080">GDB:384080</A></TD><TD>5q35-5q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=246530">LEUKOTRIENE C4 SYNTHASE; LTC4S</A><BR>
</TD>
</TR>
<TR><TD>MAN2A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136413">GDB:136413</A></TD><TD>5q21-5q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154582">MANNOSIDASE, ALPHA, II; MANA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=224100">DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE II</A><BR>
</TD>
</TR>
<TR><TD>MCC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128163">GDB:128163</A></TD><TD>5q21-5q22 5q21-5q21 5q22.1-5q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159350">MUTATED IN COLORECTAL CANCERS; MCC</A><BR>
</TD>
</TR>
<TR><TD>MCCC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135990">GDB:135990</A></TD><TD>5q12-5q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=210210">II</A><BR>
</TD>
</TR>
<TR><TD>MSH3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:641986">GDB:641986</A></TD><TD>5q11-5q12 5q11.2-5q14 5q11.2-5q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600887">MutS, E. COLI, HOMOLOG OF, 3; MSH3</A><BR>
</TD>
</TR>
<TR><TD>MSX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138766">GDB:138766</A></TD><TD>5q34-5q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123101">MSH (DROSOPHILA) HOMEO BOX HOMOLOG 2; MSX2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168500">PARIETAL FORAMINA, SYMMETRIC; PFM</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604757"></A><BR>
</TD>
</TR>
<TR><TD>NR3C1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120017">GDB:120017</A></TD><TD>5q31-5q32 5q31-5q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138040">GLUCOCORTICOID RECEPTOR; GRL</A><BR>
</TD>
</TR>
<TR><TD>PCSK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128033">GDB:128033</A></TD><TD>5q15-5q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162150">PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 1; PCSK1</A><BR>
</TD>
</TR>
<TR><TD>PDE6A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120265">GDB:120265</A></TD><TD>5q31-5q33 5q31.2-5q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180071">PHOSPHODIESTERASE 6A, cGMP-SPECIFIC, ROD, ALPHA; PDE6A</A><BR>
</TD>
</TR>
<TR><TD>PFBI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956096">GDB:9956096</A></TD><TD>5q31-5q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248310">INTENSITY OF INFECTION IN</A><BR>
</TD>
</TR>
<TR><TD>RASA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120339">GDB:120339</A></TD><TD>5q13-5q13 5q13.3-5q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139150">RAS p21 PROTEIN ACTIVATOR 1; RASA1</A><BR>
</TD>
</TR>
<TR><TD>SCZD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120370">GDB:120370</A></TD><TD>5q11.2-5q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181510">DISORDER-1; SCZD1</A><BR>
</TD>
</TR>
<TR><TD>SDHA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:378037">GDB:378037</A></TD><TD>5p15-5p15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600857">SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT A, FLAVOPROTEIN; SDHA</A><BR>
</TD>
</TR>
<TR><TD>SGCD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5886421">GDB:5886421</A></TD><TD>5q33-5q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601411">SARCOGLYCAN, DELTA; SGCD</A><BR>
</TD>
</TR>
<TR><TD>SLC22A5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9863277">GDB:9863277</A></TD><TD>5q31-5q31 5q31.1-5q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212140">CARNITINE DEFICIENCY, SYSTEMIC, DUE TO DEFECT IN RENAL REABSORPTION</A><BR>
</TD>
</TR>
<TR><TD>SLC26A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125421">GDB:125421</A></TD><TD>5q31-5q34 5q32-5q33.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222600">DIASTROPHIC DYSPLASIA; DTD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=226900">EPIPHYSEAL DYSPLASIA, MULTIPLE; MED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256050">NEONATAL OSSEOUS DYSPLASIA I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600972">ACHONDROGENESIS, TYPE IB; ACG1B</A><BR>
</TD>
</TR>
<TR><TD>SLC6A3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132445">GDB:132445</A></TD><TD>5p15.3-5p15.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126455">SOLUTE CARRIER FAMILY 6, MEMBER 3; SLC6A3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143465">DEFICIT-HYPERACTIVITY DISORDER; ADHD</A><BR>
</TD>
</TR>
<TR><TD>SM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9834488">GDB:9834488</A></TD><TD>5q31-5q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181460">SCHISTOSOMA MANSONI SUSCEPTIBILITY/RESISTANCE</A><BR>
</TD>
</TR>
<TR><TD>SMA@</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120378">GDB:120378</A></TD><TD>5q12.2-5q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253300">SPINAL MUSCULAR ATROPHY I; SMA I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600354">SURVIVAL OF MOTOR NEURON 1, TELOMERIC; SMN1</A><BR>
</TD>
</TR>
<TR><TD>SMN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5215173">GDB:5215173</A></TD><TD>5q13-5q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253300">SPINAL MUSCULAR ATROPHY I; SMA I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600354">SURVIVAL OF MOTOR NEURON 1, TELOMERIC; SMN1</A><BR>
</TD>
</TR>
<TR><TD>SMN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5215175">GDB:5215175</A></TD><TD>5q13-5q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253300">SPINAL MUSCULAR ATROPHY I; SMA I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601627">SURVIVAL OF MOTOR NEURON 2, CENTROMERIC; SMN2</A><BR>
</TD>
</TR>
<TR><TD>SPINK5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956114">GDB:9956114</A></TD><TD>5q31-5q32 5q32-5q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256500">NETHERTON DISEASE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605010"></A><BR>
</TD>
</TR>
<TR><TD>TCOF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127390">GDB:127390</A></TD><TD>5q32-5q33.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154500">TREACHER COLLINS-FRANCESCHETTI SYNDROME 1; TCOF1</A><BR>
</TD>
</TR>
<TR><TD>TELAB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11515361">GDB:11515361</A></TD><TD>5q14-5q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=187260">TELANGIECTASIA, HEREDITARY BENIGN</A><BR>
</TD>
</TR>
<TR><TD>TGFBI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:597601">GDB:597601</A></TD><TD>5q31-5q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121900">CORNEAL DYSTROPHY, GRANULAR TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122200">CORNEAL DYSTROPHY, LATTICE TYPE I; CDL1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601692">TRANSFORMING GROWTH FACTOR, BETA-INDUCED, 68 KD; TGFBI</A><BR>
</TD>
</TR>
<TR><TD>ALDH5A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:454767">GDB:454767</A></TD><TD>6p22-6p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=271980">SUCCINIC SEMIALDEHYDE DEHYDROGENASE, NAD(+)-DEPENDENT; SSADH</A><BR>
</TD>
</TR>
<TR><TD>ARG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119006">GDB:119006</A></TD><TD>6q23-6q23 6q22.3-6q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=207800">ARGININEMIA</A><BR>
</TD>
</TR>
<TR><TD>AS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135697">GDB:135697</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106300">ANKYLOSING SPONDYLITIS; AS</A><BR>
</TD>
</TR>
<TR><TD>ASSP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119017">GDB:119017</A></TD><TD>6pter-6qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215700">CITRULLINEMIA</A><BR>
</TD>
</TR>
<TR><TD>BCKDHB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118759">GDB:118759</A></TD><TD>6p22-6p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248611">MAPLE SYRUP URINE DISEASE, TYPE IB</A><BR>
</TD>
</TR>
<TR><TD>BF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119726">GDB:119726</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138470">GLYCINE-RICH BETA-GLYCOPROTEIN; GBG</A><BR>
</TD>
</TR>
<TR><TD>C2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119731">GDB:119731</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217000">COMPLEMENT COMPONENT-2, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>C4A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119732">GDB:119732</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120810">COMPLEMENT COMPONENT 4A; C4A</A><BR>
</TD>
</TR>
<TR><TD>CDKN1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:266550">GDB:266550</A></TD><TD>6p21.2-6p21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=116899">CYCLIN-DEPENDENT KINASE INHIBITOR 1A; CDKN1A</A><BR>
</TD>
</TR>
<TR><TD>COL10A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128635">GDB:128635</A></TD><TD>6q21-6q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120110">COLLAGEN, TYPE X, ALPHA 1; COL10A1</A><BR>
</TD>
</TR>
<TR><TD>COL11A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119788">GDB:119788</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120290">COLLAGEN, TYPE XI, ALPHA-2; COL11A2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=184840">STICKLER SYNDROME, TYPE II; STL2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601868">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 13; DFNA13</A><BR>
</TD>
</TR>
<TR><TD>CYP21A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120605">GDB:120605</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201910">ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>DYX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:437584">GDB:437584</A></TD><TD>6p22-6p21.3 6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600202">DYSLEXIA, SPECIFIC, 2; DYX2</A><BR>
</TD>
</TR>
<TR><TD>EJM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119864">GDB:119864</A></TD><TD>6p21.1-6p11 6p21.2-6q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254770">MYOCLONIC EPILEPSY, JUVENILE; EJM1</A><BR>
</TD>
</TR>
<TR><TD>ELOVL4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11499609">GDB:11499609</A></TD><TD>6q14-6q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600110">STARGARDT DISEASE 3; STGD3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605512"></A><BR>
</TD>
</TR>
<TR><TD>EPM2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3763331">GDB:3763331</A></TD><TD>6q23-6q25 6q23.3-6q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254780">EPILEPSY, PROGRESSIVE MYOCLONIC 2; EPM2</A><BR>
</TD>
</TR>
<TR><TD>ESR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119120">GDB:119120</A></TD><TD>6q25.1-6q25.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133430">ESTROGEN RECEPTOR; ESR</A><BR>
</TD>
</TR>
<TR><TD>EYA4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:700062">GDB:700062</A></TD><TD>6q22.3-6q23.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601316">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 10; DFNA10</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603550"></A><BR>
</TD>
</TR>
<TR><TD>F13A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120614">GDB:120614</A></TD><TD>6p25.1-6p24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134570">FACTOR XIII, A1 SUBUNIT; F13A1</A><BR>
</TD>
</TR>
<TR><TD>FANCE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1220236">GDB:1220236</A></TD><TD>6p22-6p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600901">FANCONI ANEMIA, COMPLEMENTATION GROUP E; FACE</A><BR>
</TD>
</TR>
<TR><TD>GCLC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132915">GDB:132915</A></TD><TD>6p12-6p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230450">GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE</A><BR>
</TD>
</TR>
<TR><TD>GJA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125196">GDB:125196</A></TD><TD>6q21-6q23.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121014">GAP JUNCTION PROTEIN, ALPHA-1, 43 KD; GJA1</A><BR>
</TD>
</TR>
<TR><TD>GLYS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136421">GDB:136421</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=233100">GLYCOSURIA, RENAL</A><BR>
</TD>
</TR>
<TR><TD>GMPR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127058">GDB:127058</A></TD><TD>6p23-6p23 6pter-6qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139265">GUANINE MONOPHOSPHATE REDUCTASE</A><BR>
</TD>
</TR>
<TR><TD>GSE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956235">GDB:9956235</A></TD><TD>6p-6p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212750">DISEASE; CD</A><BR>
</TD>
</TR>
<TR><TD>HCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9993306">GDB:9993306</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177900">PSORIASIS, SUSCEPTIBILITY TO</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605310"></A><BR>
</TD>
</TR>
<TR><TD>HFE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119309">GDB:119309</A></TD><TD>6p22-6p22 6p22.1-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=235200">HEMOCHROMATOSIS; HFE</A><BR>
</TD>
</TR>
<TR><TD>HLA-A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119310">GDB:119310</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142800">HLA-A HISTOCOMPATIBILITY TYPE; HLAA</A><BR>
</TD>
</TR>
<TR><TD>HLA-DPB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120636">GDB:120636</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142858">HLA-DP HISTOCOMPATIBILITY TYPE, BETA-1 SUBUNIT</A><BR>
</TD>
</TR>
<TR><TD>HLA-DRA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120641">GDB:120641</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142860">HLA-DR HISTOCOMPATIBILITY TYPE; HLA-DRA</A><BR>
</TD>
</TR>
<TR><TD>HPFH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9849006">GDB:9849006</A></TD><TD>6q23-6q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142470">HETEROCELLULAR HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN</A><BR>
</TD>
</TR>
<TR><TD>ICS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136433">GDB:136433</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=242650">IMMOTILE CILIA SYNDROME-1; ICS1</A><BR>
</TD>
</TR>
<TR><TD>IDDM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9953173">GDB:9953173</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222100">DIABETES MELLITUS, JUVENILE-ONSET INSULIN-DEPENDENT; IDDM</A><BR>
</TD>
</TR>
<TR><TD>IFNGR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120688">GDB:120688</A></TD><TD>6q23-6q24 6q24.1-6q24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107470">INTERFERON, GAMMA, RECEPTOR-1; IFNGR1</A><BR>
</TD>
</TR>
<TR><TD>IGAD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6929077">GDB:6929077</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137100">SELECTIVE DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>IGF2R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120083">GDB:120083</A></TD><TD>6q26-6q26 6q25.3-6q25.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147280">INSULIN-LIKE GROWTH FACTOR 2 RECEPTOR; IGF2R</A><BR>
</TD>
</TR>
<TR><TD>ISCW</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956158">GDB:9956158</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146850">SUPPRESSION; IS</A><BR>
</TD>
</TR>
<TR><TD>LAMA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132362">GDB:132362</A></TD><TD>6q22-6q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156225">LAMININ, ALPHA 2; LAMA2</A><BR>
</TD>
</TR>
<TR><TD>LAP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958992">GDB:9958992</A></TD><TD>6p21.3-6p21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150270">LARYNGEAL ADDUCTOR PARALYSIS; LAP</A><BR>
</TD>
</TR>
<TR><TD>LCA5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498764">GDB:11498764</A></TD><TD>6q11-6q16 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204000">AMAUROSIS CONGENITA OF LEBER I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604537"></A><BR>
</TD>
</TR>
<TR><TD>LPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120699">GDB:120699</A></TD><TD>6q26-6q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=152200">APOLIPOPROTEIN(a); LPA</A><BR>
</TD>
</TR>
<TR><TD>MCDR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131406">GDB:131406</A></TD><TD>6q14-6q16.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136550">MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE; MCDR1</A><BR>
</TD>
</TR>
<TR><TD>MOCS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9862235">GDB:9862235</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252150">MOLYBDENUM COFACTOR DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>MUT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120204">GDB:120204</A></TD><TD>6p21.2-6p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=251000">METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>MYB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119441">GDB:119441</A></TD><TD>6q22-6q22 6q23.3-6q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=189990">V-MYB AVIAN MYELOBLASTOSIS VIRAL ONCOGENE HOMOLOG; MYB</A><BR>
</TD>
</TR>
<TR><TD>NEU1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120230">GDB:120230</A></TD><TD>10pter-10q23 6p21-6p21 6pter-6qter 6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256550">NEURAMINIDASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>NKS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128100">GDB:128100</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=272370">SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS; EC1</A><BR>
</TD>
</TR>
<TR><TD>NYS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9848763">GDB:9848763</A></TD><TD>6p12-6p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164100">NYSTAGMUS, CONGENITAL</A><BR>
</TD>
</TR>
<TR><TD>OA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136429">GDB:136429</A></TD><TD>6q13-6q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203310">ALBINISM, OCULAR, AUTOSOMAL RECESSIVE; OAR</A><BR>
</TD>
</TR>
<TR><TD>ODDD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6392584">GDB:6392584</A></TD><TD>6q22-6q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164200">OCULODENTODIGITAL DYSPLASIA; ODDD</A><BR>
</TD>
</TR>
<TR><TD>OFC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120247">GDB:120247</A></TD><TD>6p24-6p24 6p23-6p23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=119530">OROFACIAL CLEFT 1; OFC1</A><BR>
</TD>
</TR>
<TR><TD>PARK2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6802742">GDB:6802742</A></TD><TD>6q25.2-6q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600116">PARKINSONISM, JUVENILE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602544"></A><BR>
</TD>
</TR>
<TR><TD>PBCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956321">GDB:9956321</A></TD><TD>6pter-6qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600089">BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS</A><BR>
</TD>
</TR>
<TR><TD>PBCRA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3763333">GDB:3763333</A></TD><TD>6q12-6q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600790">CHORIORETINAL ATROPHY, PROGRESSIVE BIFOCAL; CRAPB</A><BR>
</TD>
</TR>
<TR><TD>PDB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136349">GDB:136349</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167250">DISEASE OF BONE; PDB</A><BR>
</TD>
</TR>
<TR><TD>PEX3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955507">GDB:9955507</A></TD><TD>6q23-6q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214100">ZELLWEGER SYNDROME; ZS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603164"></A><BR>
</TD>
</TR>
<TR><TD>PEX6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5592414">GDB:5592414</A></TD><TD>6p22-6p11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214100">ZELLWEGER SYNDROME; ZS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601498">PEROXIN-6; PEX6</A><BR>
</TD>
</TR>
<TR><TD>PEX7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6155803">GDB:6155803</A></TD><TD>6q22-6q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215100">RHIZOMELIC CHONDRODYSPLASIA PUNCTATA; RCDP</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601757">PEROXIN-7; PEX7</A><BR>
</TD>
</TR>
<TR><TD>PKHD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433910">GDB:433910</A></TD><TD>6p21.2-6p12 6p12.3-6p12.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=263200">POLYCYSTIC KIDNEY AND HEPATIC DISEASE-1; PKHD1</A><BR>
</TD>
</TR>
<TR><TD>PLA2G7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958829">GDB:9958829</A></TD><TD>6p21.2-6p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601690">PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, SUBUNIT</A><BR>
</TD>
</TR>
<TR><TD>PLG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119498">GDB:119498</A></TD><TD>6q26-6q27 6q26-6q26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173350">PLASMINOGEN; PLG</A><BR>
</TD>
</TR>
<TR><TD>POLH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6963323">GDB:6963323</A></TD><TD>6p21.1-6p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278750">PIGMENTOSUM WITH NORMAL DNA REPAIR RATES</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603968"></A><BR>
</TD>
</TR>
<TR><TD>PPAC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956248">GDB:9956248</A></TD><TD>6q-6q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=208230">ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD</A><BR>
</TD>
</TR>
<TR><TD>PSORS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6381310">GDB:6381310</A></TD><TD>6p21-6p21 6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177900">PSORIASIS, SUSCEPTIBILITY TO</A><BR>
</TD>
</TR>
<TR><TD>PUJO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956231">GDB:9956231</A></TD><TD>6p-6p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143400">MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MRD</A><BR>
</TD>
</TR>
<TR><TD>RCD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:333929">GDB:333929</A></TD><TD>6q26-6q26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180020">RETINAL CONE DEGENERATION</A><BR>
</TD>
</TR>
<TR><TD>RDS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118863">GDB:118863</A></TD><TD>6p21.2-6cen 6p21.1-6cen </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179605">RETINAL DEGENERATION, SLOW; RDS</A><BR>
</TD>
</TR>
<TR><TD>RHAG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136011">GDB:136011</A></TD><TD>6p21-6qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180297">RHESUS BLOOD GROUP-ASSOCIATED GLYCOPROTEIN; RHAG</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=268150">RH-NULL, REGULATOR TYPE; RHN</A><BR>
</TD>
</TR>
<TR><TD>RP14</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433713">GDB:433713</A></TD><TD>6p21.3-6p21.2 6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600132">RETINITIS PIGMENTOSA-14; RP14</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602280">TUBBY-LIKE PROTEIN 1; TULP1</A><BR>
</TD>
</TR>
<TR><TD>RUNX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:392082">GDB:392082</A></TD><TD>6p21-6p21 6p21.1-6p12.3 6p21.2-6p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=119600">CLEIDOCRANIAL DYSPLASIA; CCD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600211">CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 1; CBFA1</A><BR>
</TD>
</TR>
<TR><TD>RWS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956195">GDB:9956195</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179450">SENSITIVITY</A><BR>
</TD>
</TR>
<TR><TD>SCA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119588">GDB:119588</A></TD><TD>6p23-6p23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164400">SPINOCEREBELLAR ATAXIA 1; SCA1</A><BR>
</TD>
</TR>
<TR><TD>SCZD3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:635974">GDB:635974</A></TD><TD>6p24-6p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600511">DISORDER-3; SCZD3</A><BR>
</TD>
</TR>
<TR><TD>SIASD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433552">GDB:433552</A></TD><TD>6q14-6q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=269920">SIALIC ACID STORAGE DISEASE; SIASD</A><BR>
</TD>
</TR>
<TR><TD>SOD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119597">GDB:119597</A></TD><TD>6q25.2-6q25.2 6q25.3-6q25.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147460">SUPEROXIDE DISMUTASE 2, MITOCHONDRIAL; SOD2</A><BR>
</TD>
</TR>
<TR><TD>ST8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6118456">GDB:6118456</A></TD><TD>6q26-6q27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167000">OVARIAN TUMOR</A><BR>
</TD>
</TR>
<TR><TD>TAP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132668">GDB:132668</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170260">TRANSPORTER 1, ABC; TAP1</A><BR>
</TD>
</TR>
<TR><TD>TAP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132669">GDB:132669</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170261">TRANSPORTER 2, ABC; TAP2</A><BR>
</TD>
</TR>
<TR><TD>TFAP2B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:681506">GDB:681506</A></TD><TD>6p12-6p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=169100">DUCTUS ARTERIOSUS; PDA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601601">TRANSCRIPTION FACTOR AP-2 BETA; TFAP2B</A><BR>
</TD>
</TR>
<TR><TD>TNDM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956265">GDB:9956265</A></TD><TD>6q22-6q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601410">DIABETES MELLITUS, TRANSIENT NEONATAL</A><BR>
</TD>
</TR>
<TR><TD>TNF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120441">GDB:120441</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191160">TUMOR NECROSIS FACTOR; TNF</A><BR>
</TD>
</TR>
<TR><TD>TPBG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125568">GDB:125568</A></TD><TD>6q14-6q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190920">TROPHOBLAST GLYCOPROTEIN; TPBG; M6P1</A><BR>
</TD>
</TR>
<TR><TD>TPMT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:209025">GDB:209025</A></TD><TD>6p22.3-6p22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=187680">THIOPURINE S-METHYLTRANSFERASE; TPMT</A><BR>
</TD>
</TR>
<TR><TD>TULP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6199353">GDB:6199353</A></TD><TD>6p21.3-6p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602280">TUBBY-LIKE PROTEIN 1; TULP1</A><BR>
</TD>
</TR>
<TR><TD>WISP3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957361">GDB:9957361</A></TD><TD>6q22-6q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=208230">ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603400"></A><BR>
</TD>
</TR>
<TR><TD>AASS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11502144">GDB:11502144</A></TD><TD>7q31.3-7q31.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238700">HYPERLYSINEMIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605113"></A><BR>
</TD>
</TR>
<TR><TD>ABCB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120712">GDB:120712</A></TD><TD>7q21-7q21 7q21.1-7q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=171050">P-GLYCOPROTEIN-1; PGY1</A><BR>
</TD>
</TR>
<TR><TD>ABCB4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120713">GDB:120713</A></TD><TD>7q21-7q21 7q21.1-7q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=171060">P-GLYCOPROTEIN-3; PGY3</A><BR>
</TD>
</TR>
<TR><TD>ACHE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118746">GDB:118746</A></TD><TD>7q22-7q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100740">ACETYLCHOLINESTERASE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=112100">BLOOD GROUP--Yt SYSTEM; YT</A><BR>
</TD>
</TR>
<TR><TD>AQP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129082">GDB:129082</A></TD><TD>7p14-7p14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107776">AQUAPORIN-1; AQP1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=110450">BLOOD GROUP--COLTON; CO</A><BR>
</TD>
</TR>
<TR><TD>ASL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119703">GDB:119703</A></TD><TD>7q21.3-7q22 7cen-7q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=207900">ARGININOSUCCINICACIDURIA</A><BR>
</TD>
</TR>
<TR><TD>ASNS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119706">GDB:119706</A></TD><TD>7q21-7q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108370">ASPARAGINE SYNTHETASE; ASNS; AS</A><BR>
</TD>
</TR>
<TR><TD>AUTS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864226">GDB:9864226</A></TD><TD>7q32-7q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=209850">DISORDER</A><BR>
</TD>
</TR>
<TR><TD>BPGM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119039">GDB:119039</A></TD><TD>7q31-7q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222800">DIPHOSPHOGLYCERATE MUTASE DEFICIENCY OF ERYTHROCYTE</A><BR>
</TD>
</TR>
<TR><TD>BRAF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127513">GDB:127513</A></TD><TD>7q34-7q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114500">CANCER OF COLON</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164757">V-RAF MURINE SARCOMA VIRAL ONCOGENE HOMOLOG B1; BRAF</A><BR>
</TD>
</TR>
<TR><TD>C7orf2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10794644">GDB:10794644</A></TD><TD>7q36-7q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=200500">ACHEIROPODY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605522"></A><BR>
</TD>
</TR>
<TR><TD>CACNA2D1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132010">GDB:132010</A></TD><TD>7q21-7q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114204">CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-2/DELTA SUBUNIT;</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154276">MALIGNANT HYPERTHERMIA SUSCEPTIBILITY-3</A><BR>
</TD>
</TR>
<TR><TD>CCM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:580824">GDB:580824</A></TD><TD>7q11.2-7q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=116860">CEREBRAL CAVERNOUS MALFORMATIONS 1; CCM1</A><BR>
</TD>
</TR>
<TR><TD>CD36</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138800">GDB:138800</A></TD><TD>7q11.2-7q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173510">CD36 ANTIGEN; CD36</A><BR>
</TD>
</TR>
<TR><TD>CFTR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120584">GDB:120584</A></TD><TD>7q31.3-7q31.3 7q31.2-7q31.3 7q31.2-7q31.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167800">PANCREATITIS, HEREDITARY; PCTT</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=219700">CYSTIC FIBROSIS; CF</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277180">DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD; CAVD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602421"></A><BR>
</TD>
</TR>
<TR><TD>CHORDOMA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498328">GDB:11498328</A></TD><TD>7q33-7q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215400"></A><BR>
</TD>
</TR>
<TR><TD>CLCN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134688">GDB:134688</A></TD><TD>7q32-7qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118425">CHLORIDE CHANNEL 1, SKELETAL MUSCLE; CLCN1</A><BR>
</TD>
</TR>
<TR><TD>CMH6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956392">GDB:9956392</A></TD><TD>7q3-7q3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600858">CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, WITH WOLFF-PARKINSON-WHITE</A><BR>
</TD>
</TR>
<TR><TD>CMT2D</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9953232">GDB:9953232</A></TD><TD>7p14-7p14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601472">CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, D</A><BR>
</TD>
</TR>
<TR><TD>COL1A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119062">GDB:119062</A></TD><TD>7q21.3-7q22.1 7q22.1-7q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120160">COLLAGEN, TYPE I, ALPHA-2 POLYPEPTIDE; COL1A2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166200">OSTEOGENESIS IMPERFECTA TYPE I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166220">OSTEOGENESIS IMPERFECTA TYPE IV; OI4</A><BR>
</TD>
</TR>
<TR><TD>CRS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119073">GDB:119073</A></TD><TD>7p21-7p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123100">CRANIOSYNOSTOSIS, TYPE 1; CRS1</A><BR>
</TD>
</TR>
<TR><TD>CYMD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:366594">GDB:366594</A></TD><TD>7p21-7p15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153880">MACULAR EDEMA, CYSTOID</A><BR>
</TD>
</TR>
<TR><TD>DFNA5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:636174">GDB:636174</A></TD><TD>7p15-7p15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600994">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 5; DFNA5</A><BR>
</TD>
</TR>
<TR><TD>DLD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120608">GDB:120608</A></TD><TD>7q31-7q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=246900">LIPOAMIDE DEHYDROGENASE DEFICIENCY, LACTIC ACIDOSIS DUE TO</A><BR>
</TD>
</TR>
<TR><TD>DYT11</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10013754">GDB:10013754</A></TD><TD>7q21-7q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159900">MYOCLONUS, HEREDITARY ESSENTIAL</A><BR>
</TD>
</TR>
<TR><TD>EEC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136338">GDB:136338</A></TD><TD>7q11.2-7q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=129900">ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE; EEC</A><BR>
</TD>
</TR>
<TR><TD>ELN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119107">GDB:119107</A></TD><TD>7q11.23-7q11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130160">ELASTIN; ELN</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194050">WILLIAMS-BEUREN SYNDROME; WBS</A><BR>
</TD>
</TR>
<TR><TD>ETV1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:335229">GDB:335229</A></TD><TD>7p22-7p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600541">ETS VARIANT GENE 1; ETV1</A><BR>
</TD>
</TR>
<TR><TD>FKBP6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955215">GDB:9955215</A></TD><TD>7q11.23-7q11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194050">WILLIAMS-BEUREN SYNDROME; WBS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604839"></A><BR>
</TD>
</TR>
<TR><TD>GCK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127550">GDB:127550</A></TD><TD>7p-7p 7p15-7p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125851">DIABETES MELLITUS, AUTOSOMAL DOMINANT, TYPE II</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125853">DIABETES MELLITUS, TYPE II</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138079">GLUCOKINASE; GCK</A><BR>
</TD>
</TR>
<TR><TD>GHRHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138465">GDB:138465</A></TD><TD>7p14-7p14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139191">GROWTH HORMONE-RELEASING HORMONE RECEPTOR; GHRHR</A><BR>
</TD>
</TR>
<TR><TD>GHS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956363">GDB:9956363</A></TD><TD>7p-7p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141400">MICROSOMIA WITH RADIAL DEFECTS</A><BR>
</TD>
</TR>
<TR><TD>GLI3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119990">GDB:119990</A></TD><TD>7p13-7p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146510">PALLISTER-HALL SYNDROME; PHS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=165240">GLI-KRUPPEL FAMILY MEMBER 3; GLI3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=174200">POSTAXIAL POLYDACTYLY, TYPE A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=175700">GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS</A><BR>
</TD>
</TR>
<TR><TD>GPDS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956410">GDB:9956410</A></TD><TD>7q35-7q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600510">GLAUCOMA, PIGMENT-DISPERSION TYPE</A><BR>
</TD>
</TR>
<TR><TD>GUSB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120025">GDB:120025</A></TD><TD>7q11.21-7q11.22 7q21.11-7q21.11 7q22-7q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253220">MUCOPOLYSACCHARIDOSIS TYPE VII</A><BR>
</TD>
</TR>
<TR><TD>HLXB9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136411">GDB:136411</A></TD><TD>1q41-1q42.1 7q36-7q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142994">HOMEO BOX GENE HB9; HLXB9</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176450">SACRAL AGENESIS, HEREDITARY, WITH PRESACRAL MASS, ANTERIOR MENINGOCELE,</A><BR>
</TD>
</TR>
<TR><TD>HOXA13</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120656">GDB:120656</A></TD><TD>7p15-7p14 7p15.3-7p15.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142959">HOMEO BOX A13; HOXA13</A><BR>
</TD>
</TR>
<TR><TD>HPFH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128071">GDB:128071</A></TD><TD>7q36-7q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142335">HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, HETEROCELLULAR, INDIAN</A><BR>
</TD>
</TR>
<TR><TD>HRX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958999">GDB:9958999</A></TD><TD>7q-7q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145290">HRX</A><BR>
</TD>
</TR>
<TR><TD>IAB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498909">GDB:11498909</A></TD><TD>7q11-7q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105800">ANEURYSM, INTRACRANIAL BERRY</A><BR>
</TD>
</TR>
<TR><TD>IMMP2L</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11499195">GDB:11499195</A></TD><TD>7q31-7q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137580">GILLES DE LA TOURETTE SYNDROME; GTS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605977"></A><BR>
</TD>
</TR>
<TR><TD>KCNH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138126">GDB:138126</A></TD><TD>7q35-7q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=152427">LONG QT SYNDROME, TYPE 2; LQT2</A><BR>
</TD>
</TR>
<TR><TD>LAMB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119357">GDB:119357</A></TD><TD>7q22-7q22 7q31.1-7q31.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150240">LAMININ BETA 1; LAMB1</A><BR>
</TD>
</TR>
<TR><TD>LEP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136420">GDB:136420</A></TD><TD>7q31.3-7q31.3 7q32.1-7q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164160">LEPTIN; LEP</A><BR>
</TD>
</TR>
<TR><TD>MET</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120178">GDB:120178</A></TD><TD>7q31-7q31 7q31.2-7q31.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114550">CANCER, HEPATOCELLULAR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164860">MET PROTO-ONCOGENE; MET</A><BR>
</TD>
</TR>
<TR><TD>NCF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120222">GDB:120222</A></TD><TD>7q11.23-7q11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=233700">GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-POSITIVE FORM</A><BR>
</TD>
</TR>
<TR><TD>NM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119454">GDB:119454</A></TD><TD>7q22-7qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162820">NEUTROPHIL CHEMOTACTIC RESPONSE; NCR</A><BR>
</TD>
</TR>
<TR><TD>OGDH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118847">GDB:118847</A></TD><TD>7p13-7p11.2 7p14-7p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203740">ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>OPN1SW</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119032">GDB:119032</A></TD><TD>7q31.3-7q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190900">TRITANOPIA</A><BR>
</TD>
</TR>
<TR><TD>PEX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9787110">GDB:9787110</A></TD><TD>7q21-7q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214100">ZELLWEGER SYNDROME; ZS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602136">PEROXIN-1; PEX1</A><BR>
</TD>
</TR>
<TR><TD>PGAM2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120280">GDB:120280</A></TD><TD>7p13-7p12 7p13-7p12.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261670">PHOSPHOGLYCERATE MUTASE, DEFICIENCY OF M SUBUNIT OF</A><BR>
</TD>
</TR>
<TR><TD>PMS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:386406">GDB:386406</A></TD><TD>7p22-7p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600259">POSTMEIOTIC SEGREGATION INCREASED (S. CEREVISIAE)-2; PMS2</A><BR>
</TD>
</TR>
<TR><TD>PON1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120308">GDB:120308</A></TD><TD>7q21-7q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168820">PARAOXONASE 1; PON1</A><BR>
</TD>
</TR>
<TR><TD>PPP1R3A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136797">GDB:136797</A></TD><TD>7q31.2-7q31.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600917">PROTEIN PHOSPHATASE 1, REGULATORY (INHIBITOR) SUBUNIT 3; PPP1R3</A><BR>
</TD>
</TR>
<TR><TD>PRSS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119620">GDB:119620</A></TD><TD>7q32-7qter 7q35-7q35 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167800">PANCREATITIS, HEREDITARY; PCTT</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276000">PROTEASE, SERINE, 1; PRSS1</A><BR>
</TD>
</TR>
<TR><TD>PTC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118744">GDB:118744</A></TD><TD>7q-7q 7q33-7q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=171200">PHENYLTHIOCARBAMIDE TASTING</A><BR>
</TD>
</TR>
<TR><TD>PTPN12</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136846">GDB:136846</A></TD><TD>7q11.23-7q11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600079">PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR TYPE, 12; PTPN12</A><BR>
</TD>
</TR>
<TR><TD>RP10</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138786">GDB:138786</A></TD><TD>7q-7q 7q31-7q33 7q31-7q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180105">RETINITIS PIGMENTOSA-10; RP10</A><BR>
</TD>
</TR>
<TR><TD>RP9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:333931">GDB:333931</A></TD><TD>7p-7p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180104">RETINITIS PIGMENTOSA-9; RP9</A><BR>
</TD>
</TR>
<TR><TD>SERPINE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120297">GDB:120297</A></TD><TD>7q22.1-7q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173360">PLASMINOGEN ACTIVATOR INHIBITOR, TYPE I; PAI1</A><BR>
</TD>
</TR>
<TR><TD>SGCE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958714">GDB:9958714</A></TD><TD>7q21-7q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159900">MYOCLONUS, HEREDITARY ESSENTIAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604149"></A><BR>
</TD>
</TR>
<TR><TD>SHFM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128195">GDB:128195</A></TD><TD>7q21.3-7q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=183600">SPLIT-HAND/FOOT DEFORMITY, TYPE I; SHFD1</A><BR>
</TD>
</TR>
<TR><TD>SHH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:456309">GDB:456309</A></TD><TD>7q36-7q36 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142945">HOLOPROSENCEPHALY, TYPE 3; HPE3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600725">SONIC HEDGEHOG, DROSOPHILA, HOMOLOG OF; SHH</A><BR>
</TD>
</TR>
<TR><TD>SLC26A3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138165">GDB:138165</A></TD><TD>7q22-7q31.1 7q31-7q31 7q22.3-7q31.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126650">DOWN-REGULATED IN ADENOMA; DRA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214700">CHLORIDE DIARRHEA, FAMILIAL; CLD</A><BR>
</TD>
</TR>
<TR><TD>SLC26A4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5584511">GDB:5584511</A></TD><TD>7q21-7q34 7q31-7q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=274600">PENDRED SYNDROME; PDS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600791">DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 4; DFNB4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603545"></A><BR>
</TD>
</TR>
<TR><TD>SLOS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:385950">GDB:385950</A></TD><TD>7q32-7q32 7q32.1-7q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=270400">SMITH-LEMLI-OPITZ SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>SMAD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3763345">GDB:3763345</A></TD><TD>7p14-7p14 7pter-7pter 7p15.2-7p14.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600794">SPINAL MUSCULAR ATROPHY, DISTAL, WITH UPPER LIMB PREDOMINANCE; SMAD1</A><BR>
</TD>
</TR>
<TR><TD>TBXAS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128744">GDB:128744</A></TD><TD>7q34-7q35 7q33-7q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=274180">THROMBOXANE A SYNTHASE 1; TBXAS1</A><BR>
</TD>
</TR>
<TR><TD>TWIST</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135694">GDB:135694</A></TD><TD>7p21.2-7p21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101400">ACROCEPHALOSYNDACTYLY TYPE III</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601622">TWIST, DROSOPHILA, HOMOLOG OF; TWIST</A><BR>
</TD>
</TR>
<TR><TD>ZWS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120511">GDB:120511</A></TD><TD>7q11-7q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214100">ZELLWEGER SYNDROME; ZS</A><BR>
</TD>
</TR>
<TR><TD>ACHM3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9120558">GDB:9120558</A></TD><TD>8q21-8q22 8q21-8q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=262300">PINGELAPESE BLINDNESS</A><BR>
</TD>
</TR>
<TR><TD>ADRB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:203869">GDB:203869</A></TD><TD>8p12-8p11.1 8p12-8p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109691">BETA-3-ADRENERGIC RECEPTOR; ADRB3</A><BR>
</TD>
</TR>
<TR><TD>ANK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118737">GDB:118737</A></TD><TD>8p11.2-8p11.2 8p12-8p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182900">SPHEROCYTOSIS, HEREDITARY; HS</A><BR>
</TD>
</TR>
<TR><TD>CA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119047">GDB:119047</A></TD><TD>8q22-8q22 8q13-8q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114800">CARBONIC ANHYDRASE I, ERYTHROCYTE, ELECTROPHORETIC VARIANTS OF; CA1</A><BR>
</TD>
</TR>
<TR><TD>CA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119739">GDB:119739</A></TD><TD>8q22-8q22 8q13-8q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=259730">OSTEOPETROSIS WITH RENAL TUBULAR ACIDOSIS</A><BR>
</TD>
</TR>
<TR><TD>CCAL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:512892">GDB:512892</A></TD><TD>8q-8q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600668">CHONDROCALCINOSIS WITH EARLY-ONSET OSTEOARTHRITIS; CCAL2</A><BR>
</TD>
</TR>
<TR><TD>CLN8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:252118">GDB:252118</A></TD><TD>8p23-8p23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600143">EPILEPSY, PROGRESSIVE, WITH MENTAL RETARDATION; EPMR</A><BR>
</TD>
</TR>
<TR><TD>CMT4A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138755">GDB:138755</A></TD><TD>8q-8q 8q13-8q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214400">CHARCOT-MARIE-TOOTH NEUROPATHY 4A; CMT4A</A><BR>
</TD>
</TR>
<TR><TD>CNGB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9993286">GDB:9993286</A></TD><TD>8q21-8q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=262300">PINGELAPESE BLINDNESS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605080"></A><BR>
</TD>
</TR>
<TR><TD>COH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:252122">GDB:252122</A></TD><TD>8q22-8q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=216550">COHEN SYNDROME; COH1</A><BR>
</TD>
</TR>
<TR><TD>CPP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119798">GDB:119798</A></TD><TD>8q21.13-8q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=117700">CERULOPLASMIN; CP</A><BR>
</TD>
</TR>
<TR><TD>CRH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119804">GDB:119804</A></TD><TD>8q13-8q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122560">CORTICOTROPIN-RELEASING HORMONE; CRH</A><BR>
</TD>
</TR>
<TR><TD>CYP11B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120603">GDB:120603</A></TD><TD>8q21-8q21 8q21-8q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=202010">ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 11-@BETA-HYDROXYLASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>CYP11B2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120514">GDB:120514</A></TD><TD>8q21-8q21 8q21-8q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=124080">CYTOCHROME P450, SUBFAMILY XIB, POLYPEPTIDE 2; CYP11B2</A><BR>
</TD>
</TR>
<TR><TD>DECR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:453934">GDB:453934</A></TD><TD>8q21.3-8q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222745">2,4-@DIENOYL-CoA REDUCTASE; DECR</A><BR>
</TD>
</TR>
<TR><TD>DPYS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5885803">GDB:5885803</A></TD><TD>8q22-8q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222748">DIHYDROPYRIMIDINASE; DPYS</A><BR>
</TD>
</TR>
<TR><TD>DURS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958126">GDB:9958126</A></TD><TD>8q13-8q13 8q13.1-8q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126800">DUANE SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>EBS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119856">GDB:119856</A></TD><TD>8q24-8qter 8pter-8qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131950">EPIDERMOLYSIS BULLOSA SIMPLEX, OGNA TYPE</A><BR>
</TD>
</TR>
<TR><TD>ECA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10796318">GDB:10796318</A></TD><TD>8q24-8q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600131">JUVENILE ABSENCE</A><BR>
</TD>
</TR>
<TR><TD>EGI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128830">GDB:128830</A></TD><TD>8q24-8q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600669">EPILEPSY, GENERALIZED, IDIOPATHIC; EGI</A><BR>
</TD>
</TR>
<TR><TD>EXT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135994">GDB:135994</A></TD><TD>8q24.11-8q24.11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133700">EXOSTOSES, MULTIPLE, TYPE I; EXT1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215300">CHONDROSARCOMA</A><BR>
</TD>
</TR>
<TR><TD>EYA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5215167">GDB:5215167</A></TD><TD>8q13.3-8q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113650">BRANCHIOOTORENAL DYSPLASIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601653">EYES ABSENT 1; EYA1</A><BR>
</TD>
</TR>
<TR><TD>FGFR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119913">GDB:119913</A></TD><TD>8p12-8p12 8p11.2-8p11.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101600">ACROCEPHALOSYNDACTYLY TYPE V</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136350">FIBROBLAST GROWTH FACTOR RECEPTOR-1; FGFR1</A><BR>
</TD>
</TR>
<TR><TD>GNRH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:133746">GDB:133746</A></TD><TD>8p21-8p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=152760">GONADOTROPIN-RELEASING HORMONE 1; GNRH1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227200">FAMILIAL HYPOGONADOTROPHIC</A><BR>
</TD>
</TR>
<TR><TD>GSR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119288">GDB:119288</A></TD><TD>8p21.1-8p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138300">GLUTATHIONE REDUCTASE; GSR</A><BR>
</TD>
</TR>
<TR><TD>GULOP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128078">GDB:128078</A></TD><TD>8p21.1-8p21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=240400">SCURVY</A><BR>
</TD>
</TR>
<TR><TD>HR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:595499">GDB:595499</A></TD><TD>8p12-8p12 8p21.2-8p21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203655">ALOPECIA UNIVERSALIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=209500">ATRICHIA WITH PAPULAR LESIONS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602302">HAIRLESS, MOUSE, HOMOLOG OF</A><BR>
</TD>
</TR>
<TR><TD>KCNQ3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9787230">GDB:9787230</A></TD><TD>8q24.22-8q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121201">CONVULSIONS, BENIGN FAMILIAL NEONATAL, TYPE 2; BFNC2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602232">POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY Q, MEMBER 3</A><BR>
</TD>
</TR>
<TR><TD>KFM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265291">GDB:265291</A></TD><TD>8q22.2-8q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148900">KLIPPEL-FEIL SYNDROME; KFS; KFM</A><BR>
</TD>
</TR>
<TR><TD>KWE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9315120">GDB:9315120</A></TD><TD>8p23-8p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148370">KERATOLYTIC WINTER ERYTHEMA</A><BR>
</TD>
</TR>
<TR><TD>LGCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120698">GDB:120698</A></TD><TD>8q24.11-8q24.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150230">LANGER-GIEDION SYNDROME; LGS</A><BR>
</TD>
</TR>
<TR><TD>LPL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120700">GDB:120700</A></TD><TD>8p22-8p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238600">HYPERLIPOPROTEINEMIA, TYPE I</A><BR>
</TD>
</TR>
<TR><TD>MCPH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9834525">GDB:9834525</A></TD><TD>8p23-8p23 8pter-8p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=251200">MICROCEPHALY; MCT</A><BR>
</TD>
</TR>
<TR><TD>MOS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119396">GDB:119396</A></TD><TD>8q11-8q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190060">TRANSFORMATION GENE: ONCOGENE MOS</A><BR>
</TD>
</TR>
<TR><TD>MYC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120208">GDB:120208</A></TD><TD>8q24.12-8q24.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190080">TRANSFORMATION GENE: ONCOGENE MYC; MYC</A><BR>
</TD>
</TR>
<TR><TD>NAT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125364">GDB:125364</A></TD><TD>8p23.1-8p21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108345">ARYLAMIDE ACETYLASE 1; AAC1</A><BR>
</TD>
</TR>
<TR><TD>NAT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125365">GDB:125365</A></TD><TD>8p22-8p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=243400">ISONIAZID INACTIVATION</A><BR>
</TD>
</TR>
<TR><TD>NBS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9598211">GDB:9598211</A></TD><TD>8q21-8q21 8q21-8q24 8q21.3-8q21.3 8q21.13-8q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=251260">NIJMEGEN BREAKAGE SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602667"></A><BR>
</TD>
</TR>
<TR><TD>PLAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119496">GDB:119496</A></TD><TD>8p12-8p11 8p12-8p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173370">PLASMINOGEN ACTIVATOR, TISSUE; PLAT</A><BR>
</TD>
</TR>
<TR><TD>PLEC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4119073">GDB:4119073</A></TD><TD>8q24-8q24 8q24.13-8qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=226670">EPIDERMOLYSIS BULLOSA SIMPLEX AND LIMB-GIRDLE MUSCULAR DYSTROPHY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601282">PLECTIN 1; PLEC1</A><BR>
</TD>
</TR>
<TR><TD>PRKDC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:234702">GDB:234702</A></TD><TD>8q11-8q11 8q12-8q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=202500">SEVERE COMBINED IMMUNODEFICIENCY DISEASE-1; SCID1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600899">PROTEIN KINASE, DNA-ACTIVATED, CATALYTIC SUBUNIT; PRKDC</A><BR>
</TD>
</TR>
<TR><TD>PXMP3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131487">GDB:131487</A></TD><TD>8q21.1-8q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170993">PEROXIN-2; PEX2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214100">ZELLWEGER SYNDROME; ZS</A><BR>
</TD>
</TR>
<TR><TD>RP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120352">GDB:120352</A></TD><TD>8p11-8q21 8q12-8q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180100">RETINITIS PIGMENTOSA-1; RP1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603937"></A><BR>
</TD>
</TR>
<TR><TD>SCZD6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864736">GDB:9864736</A></TD><TD>8p21-8p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181500">DISORDER-2; SCZD2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603013"></A><BR>
</TD>
</TR>
<TR><TD>SFTPC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120373">GDB:120373</A></TD><TD>8p21-8p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=178620">PULMONARY SURFACTANT APOPROTEIN PSP-C</A><BR>
</TD>
</TR>
<TR><TD>SGM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135350">GDB:135350</A></TD><TD>8q-8q 8q22.2-8q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148900">KLIPPEL-FEIL SYNDROME; KFS; KFM</A><BR>
</TD>
</TR>
<TR><TD>SPG5A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250332">GDB:250332</A></TD><TD>8p11-8q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=270800">SPASTIC PARAPLEGIA-5A, AUTOSOMAL RECESSIVE; SPG5A</A><BR>
</TD>
</TR>
<TR><TD>STAR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:635457">GDB:635457</A></TD><TD>8p11.2-8p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600617">STEROIDOGENIC ACUTE REGULATORY PROTEIN; STAR</A><BR>
</TD>
</TR>
<TR><TD>TG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120434">GDB:120434</A></TD><TD>8q24-8q24 8q24.2-8q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188450">THYROGLOBULIN; TG</A><BR>
</TD>
</TR>
<TR><TD>TRPS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:594960">GDB:594960</A></TD><TD>8q24.1-8q24.1 8q24.12-8q24.12 8q24.11-8q24.11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190350">TRICHORHINOPHALANGEAL SYNDROME, TYPE I; TRPS1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604386"></A><BR>
</TD>
</TR>
<TR><TD>TTPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:512364">GDB:512364</A></TD><TD>8q13-8q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277460">VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF; VED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600415">TOCOPHEROL (ALPHA) TRANSFER PROTEIN; TTPA</A><BR>
</TD>
</TR>
<TR><TD>VMD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119631">GDB:119631</A></TD><TD>8q-8q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153840">MACULAR DYSTROPHY, ATYPICAL VITELLIFORM; VMD1</A><BR>
</TD>
</TR>
<TR><TD>WRN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128446">GDB:128446</A></TD><TD>8p12-8p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277700">WERNER SYNDROME; WRN</A><BR>
</TD>
</TR>
<TR><TD>ABCA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:305294">GDB:305294</A></TD><TD>9q22-9q31 9q31.1-9q31.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=205400">ANALPHALIPOPROTEINEMIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600046">ATP-BINDING CASSETTE 1; ABC1</A><BR>
</TD>
</TR>
<TR><TD>ABL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119640">GDB:119640</A></TD><TD>9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=189980">ABELSON MURINE LEUKEMIA VIRAL ONCOGENE HOMOLOG 1; ABL1</A><BR>
</TD>
</TR>
<TR><TD>ABO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118956">GDB:118956</A></TD><TD>9q34.1-9q34.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=110300">ABO BLOOD GROUP; ABO</A><BR>
</TD>
</TR>
<TR><TD>ADAMTS13</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956467">GDB:9956467</A></TD><TD>9q34-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=274150">THROMBOCYTOPENIC PURPURA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604134"></A><BR>
</TD>
</TR>
<TR><TD>AK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119664">GDB:119664</A></TD><TD>9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103000">ADENYLATE KINASE-1; AK1</A><BR>
</TD>
</TR>
<TR><TD>ALAD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119665">GDB:119665</A></TD><TD>9q32-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125270">DELTA-AMINOLEVULINATE DEHYDRATASE; ALAD</A><BR>
</TD>
</TR>
<TR><TD>ALDH1A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119667">GDB:119667</A></TD><TD>9q21-9q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100640">ALDEHYDE DEHYDROGENASE-1; ALDH1</A><BR>
</TD>
</TR>
<TR><TD>ALDOB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119669">GDB:119669</A></TD><TD>9q22-9q22 9q22.3-9q22.3 9q22.3-9q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=229600">FRUCTOSE INTOLERANCE, HEREDITARY</A><BR>
</TD>
</TR>
<TR><TD>AMBP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120696">GDB:120696</A></TD><TD>9q32-9q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176870">PROTEIN HC; HCP</A><BR>
</TD>
</TR>
<TR><TD>AMCD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:437519">GDB:437519</A></TD><TD>9p22-9q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108120">ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE 1; AMCD1</A><BR>
</TD>
</TR>
<TR><TD>ASS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119010">GDB:119010</A></TD><TD>9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215700">CITRULLINEMIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603470"></A><BR>
</TD>
</TR>
<TR><TD>BDMF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954424">GDB:9954424</A></TD><TD>9p22-9p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=112250">BONE DYSPLASIA WITH MEDULLARY FIBROSARCOMA</A><BR>
</TD>
</TR>
<TR><TD>BSCL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957720">GDB:9957720</A></TD><TD>9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=269700">SEIP SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606166"></A><BR>
</TD>
</TR>
<TR><TD>C5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119734">GDB:119734</A></TD><TD>9q33-9q33 9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120900">COMPLEMENT COMPONENT-5, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>CDKN2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:335362">GDB:335362</A></TD><TD>9p21-9p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=155601">MELANOMA, CUTANEOUS MALIGNANT, 2; CMM2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600160">CYCLIN-DEPENDENT KINASE INHIBITOR 2A; CDKN2A</A><BR>
</TD>
</TR>
<TR><TD>CHAC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6268491">GDB:6268491</A></TD><TD>9q21-9q21 9q21.32-9q21.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=200150">CHOREOACANTHOCYTOSIS; CHAC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605978"></A><BR>
</TD>
</TR>
<TR><TD>CLA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119781">GDB:119781</A></TD><TD>9q34.2-9qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=213200">CEREBELLOPARENCHYMAL DISORDER III</A><BR>
</TD>
</TR>
<TR><TD>CMD1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:677147">GDB:677147</A></TD><TD>9q13-9q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600884">CARDIOMYOPATHY, DILATED 1B; CMD1B</A><BR>
</TD>
</TR>
<TR><TD>COL5A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131457">GDB:131457</A></TD><TD>9q34.3-9q34.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120215">COLLAGEN, TYPE V, ALPHA-1 POLYPEPTIDE; COL5A1</A><BR>
</TD>
</TR>
<TR><TD>CRAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:359759">GDB:359759</A></TD><TD>9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600184">CARNITINE ACETYLTRANSFERASE; CRAT</A><BR>
</TD>
</TR>
<TR><TD>DBH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119836">GDB:119836</A></TD><TD>9q34.3-9q34.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=223360">DOPAMINE BETA-HYDROXYLASE, PLASMA; DBH</A><BR>
</TD>
</TR>
<TR><TD>DNAI1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11500297">GDB:11500297</A></TD><TD>9p21-9p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=242650">IMMOTILE CILIA SYNDROME-1; ICS1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604366"></A><BR>
</TD>
</TR>
<TR><TD>DYS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:137085">GDB:137085</A></TD><TD>9q31-9q33 9q31-9q31 9q31.2-9q31.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=223900">DYSAUTONOMIA, FAMILIAL; DYS</A><BR>
</TD>
</TR>
<TR><TD>DYT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119854">GDB:119854</A></TD><TD>9q34-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=128100">DYSTONIA 1, TORSION; DYT1</A><BR>
</TD>
</TR>
<TR><TD>ENG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:137193">GDB:137193</A></TD><TD>9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131195">ENDOGLIN; ENG</A><BR>
</TD>
</TR>
<TR><TD>FANCC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132672">GDB:132672</A></TD><TD>9q22.3-9q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227645">FANCONI ANEMIA, COMPLEMENTATION GROUP C; FACC</A><BR>
</TD>
</TR>
<TR><TD>FBP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:141539">GDB:141539</A></TD><TD>9q22.3-9q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=229700">FRUCTOSE-1,6-BISPHOPHATASE 1; FBP1</A><BR>
</TD>
</TR>
<TR><TD>FCMD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250412">GDB:250412</A></TD><TD>9q31-9q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253800">FUKUYAMA-TYPE CONGENITAL MUSCULAR DYSTROPHY; FCMD</A><BR>
</TD>
</TR>
<TR><TD>FRDA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119951">GDB:119951</A></TD><TD>9q13-9q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=229300">FRIEDREICH ATAXIA 1; FRDA1</A><BR>
</TD>
</TR>
<TR><TD>GALT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119971">GDB:119971</A></TD><TD>9p13-9p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230400">GALACTOSEMIA</A><BR>
</TD>
</TR>
<TR><TD>GLDC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128611">GDB:128611</A></TD><TD>9p24-9p23 9p22-9p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238300">HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE I; NKH1</A><BR>
</TD>
</TR>
<TR><TD>GNE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954891">GDB:9954891</A></TD><TD>9p13-9p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600737">INCLUSION BODY MYOPATHY; IBM2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603824"></A><BR>
</TD>
</TR>
<TR><TD>GSM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9784210">GDB:9784210</A></TD><TD>9q13-9q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190100">GENIOSPASM 1; GSM1</A><BR>
</TD>
</TR>
<TR><TD>GSN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120019">GDB:120019</A></TD><TD>9q33-9q33 9q34-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105120">AMYLOIDOSIS V</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137350">GELSOLIN; GSN</A><BR>
</TD>
</TR>
<TR><TD>HSD17B3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:347487">GDB:347487</A></TD><TD>9q22-9q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264300">PSEUDOHERMAPHRODITISM, MALE, WITH GYNECOMASTIA</A><BR>
</TD>
</TR>
<TR><TD>HSN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3853677">GDB:3853677</A></TD><TD>9q22.1-9q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162400">NEUROPATHY, HEREDITARY SENSORY, TYPE 1</A><BR>
</TD>
</TR>
<TR><TD>IBM2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3801447">GDB:3801447</A></TD><TD>9p1-9q1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600737">INCLUSION BODY MYOPATHY; IBM2</A><BR>
</TD>
</TR>
<TR><TD>INVS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11508405">GDB:11508405</A></TD><TD>9q31-9q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=243305">OF EMBRYONIC TURNING; INV</A><BR>
</TD>
</TR>
<TR><TD>JBTS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11517688">GDB:11517688</A></TD><TD>9q34.3-9q34.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=213300">CEREBELLOPARENCHYMAL DISORDER IV; CPD IV</A><BR>
</TD>
</TR>
<TR><TD>LALL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954426">GDB:9954426</A></TD><TD>9p22-9p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=247640">LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES; LALL</A><BR>
</TD>
</TR>
<TR><TD>LCCS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11517724">GDB:11517724</A></TD><TD>9q34-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253310">LETHAL CONGENITAL CONTRACTURE SYNDROME; LCCS</A><BR>
</TD>
</TR>
<TR><TD>LCCS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:386141">GDB:386141</A></TD><TD>9q33-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253310">LETHAL CONGENITAL CONTRACTURE SYNDROME; LCCS</A><BR>
</TD>
</TR>
<TR><TD>LGMD2H</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9862233">GDB:9862233</A></TD><TD>9q31-9q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254110">DYSTROPHY, HUTTERITE TYPE</A><BR>
</TD>
</TR>
<TR><TD>LMX1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9834526">GDB:9834526</A></TD><TD>9q32-9q34.1 9q34.1-9q34.1 9q33.3-9q34.12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=161200">NAIL-PATELLA SYNDROME; NPS1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602575"></A><BR>
</TD>
</TR>
<TR><TD>MLLT3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138172">GDB:138172</A></TD><TD>9p22-9p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159558">MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 3; MLLT3</A><BR>
</TD>
</TR>
<TR><TD>MROS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954430">GDB:9954430</A></TD><TD>9p11-9p11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=155900">MELKERSSON SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>MSSE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128019">GDB:128019</A></TD><TD>9q22.2-9q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=132800">EPITHELIOMA, SELF-HEALING SQUAMOUS</A><BR>
</TD>
</TR>
<TR><TD>NOTCH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131400">GDB:131400</A></TD><TD>9q34.3-9q34.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190198">NOTCH, DROSOPHILA, HOMOLOG OF, 1; NOTCH1</A><BR>
</TD>
</TR>
<TR><TD>ORM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120250">GDB:120250</A></TD><TD>9q32-9q32 9q34.1-9q34.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138600">OROSOMUCOID 1; ORM1</A><BR>
</TD>
</TR>
<TR><TD>PAPPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134729">GDB:134729</A></TD><TD>9q33.1-9q33.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176385">PREGNANCY-ASSOCIATED PLASMA PROTEIN A; PAPPA</A><BR>
</TD>
</TR>
<TR><TD>PIP5K1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:686238">GDB:686238</A></TD><TD>9q13-9q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=229300">FRIEDREICH ATAXIA 1; FRDA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602745"></A><BR>
</TD>
</TR>
<TR><TD>PTCH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119447">GDB:119447</A></TD><TD>9q22.1-9q22.3 9q22.3-9q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109400">BASAL CELL NEVUS SYNDROME; BCNS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601309">PATCHED, DROSOPHILA, HOMOLOG OF; PTCH</A><BR>
</TD>
</TR>
<TR><TD>PTGS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128070">GDB:128070</A></TD><TD>9q32-9q33.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176805">PROSTAGLANDIN-ENDOPEROXIDASE SYNTHASE 1; PTGS1</A><BR>
</TD>
</TR>
<TR><TD>RLN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119552">GDB:119552</A></TD><TD>9pter-9q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179730">RELAXIN; RLN1</A><BR>
</TD>
</TR>
<TR><TD>RLN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119553">GDB:119553</A></TD><TD>9pter-9q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179740">RELAXIN, OVARIAN, OF PREGNANCY</A><BR>
</TD>
</TR>
<TR><TD>RMRP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120348">GDB:120348</A></TD><TD>9p21-9p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157660">MITOCHONDRIAL RNA-PROCESSING ENDORIBONUCLEASE, RNA COMPONENT OF; RMRP;</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250250">CARTILAGE-HAIR HYPOPLASIA; CHH</A><BR>
</TD>
</TR>
<TR><TD>ROR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136454">GDB:136454</A></TD><TD>9q22.1-9q22.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113000">BRACHYDACTYLY, TYPE B; BDB</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=268310">ROBINOW SYNDROME, RECESSIVE FORM</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602337">NEUROTROPHIC TYROSINE KINASE, RECEPTOR-RELATED 2; NTRKR2</A><BR>
</TD>
</TR>
<TR><TD>RPD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954440">GDB:9954440</A></TD><TD>9q34-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601850">RETINITIS PIGMENTOSA-DEAFNESS SYNDROME 1, AUTOSOMAL DOMINANT</A><BR>
</TD>
</TR>
<TR><TD>SARDH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9835149">GDB:9835149</A></TD><TD>9q33-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=268900">SARCOSINEMIA</A><BR>
</TD>
</TR>
<TR><TD>SPTLC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957656">GDB:9957656</A></TD><TD>9q22.1-9q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162400">NEUROPATHY, HEREDITARY SENSORY, TYPE 1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605712"></A><BR>
</TD>
</TR>
<TR><TD>STOM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128993">GDB:128993</A></TD><TD>9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133090">ERYTHROCYTE SURFACE PROTEIN BAND 7.2; EPB72</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=185000">STOMATOCYTOSIS I</A><BR>
</TD>
</TR>
<TR><TD>TDFA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954420">GDB:9954420</A></TD><TD>9pter-9p22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154230">FACTOR, AUTOSOMAL</A><BR>
</TD>
</TR>
<TR><TD>TEK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:344185">GDB:344185</A></TD><TD>9p21-9p21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600195">VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL; VMCM</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600221">TEK TYROSINE KINASE, ENDOTHELIAL; TEK</A><BR>
</TD>
</TR>
<TR><TD>TMC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:636178">GDB:636178</A></TD><TD>9q13-9q21 9q21-9q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600974">DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 7; DFNB7</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606705"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606706"></A><BR>
</TD>
</TR>
<TR><TD>TRIM32</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957765">GDB:9957765</A></TD><TD>9q33.1-9q33.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254110">DYSTROPHY, HUTTERITE TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602290">TAT INTERACTIVE PROTEIN, 72 KD</A><BR>
</TD>
</TR>
<TR><TD>TSC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120735">GDB:120735</A></TD><TD>9q34-9q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191100">TUBEROUS SCLEROSIS-1; TSC1</A><BR>
</TD>
</TR>
<TR><TD>TYRP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126337">GDB:126337</A></TD><TD>9p23-9p23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115501">TYROSINASE-RELATED PROTEIN 1; TYRP1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203290">ALBINISM III</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278400">XANTHISM</A><BR>
</TD>
</TR>
<TR><TD>XPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125363">GDB:125363</A></TD><TD>9q22.3-9q22.3 9q34.1-9q34.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278700">XERODERMA PIGMENTOSUM I</A><BR>
</TD>
</TR>
<TR><TD>CACNB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132014">GDB:132014</A></TD><TD>10p12-10p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600003">CALCIUM CHANNEL, VOLTAGE-DEPENDENT, BETA-2 SUBUNIT; CACNB2</A><BR>
</TD>
</TR>
<TR><TD>COL17A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131396">GDB:131396</A></TD><TD>10q24.3-10q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113811">COLLAGEN, TYPE XVII, ALPHA-1 POLYPEPTIDE; COL17A1</A><BR>
</TD>
</TR>
<TR><TD>CUBN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:636049">GDB:636049</A></TD><TD>10p12.1-10p12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261100">MEGALOBLASTIC ANEMIA 1; MGA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602997"></A><BR>
</TD>
</TR>
<TR><TD>CXCL12</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433267">GDB:433267</A></TD><TD>10q11.1-10q11.1 10q11.2-10q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600835">STROMAL CELL-DERIVED FACTOR 1; SDF1</A><BR>
</TD>
</TR>
<TR><TD>CYP17</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119829">GDB:119829</A></TD><TD>10q24.3-10q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=202110">ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>CYP2C19</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119831">GDB:119831</A></TD><TD>10q24.1-10q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=124020">CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19</A><BR>
</TD>
</TR>
<TR><TD>CYP2C9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131455">GDB:131455</A></TD><TD>10q24.1-10q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601130">CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 9; CYP2C9</A><BR>
</TD>
</TR>
<TR><TD>EGR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120611">GDB:120611</A></TD><TD>10q21.1-10q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=129010">EARLY GROWTH RESPONSE-2; EGR2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145900">HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS</A><BR>
</TD>
</TR>
<TR><TD>EMX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:277886">GDB:277886</A></TD><TD>10q26.1-10q26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600035">EMPTY SPIRACLES, DROSOPHILA, 2, HOMOLOG OF; EMX2</A><BR>
</TD>
</TR>
<TR><TD>ERCC6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119882">GDB:119882</A></TD><TD>10q11-10q21 10q11-10q11 10q21.1-10q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133540">EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION</A><BR>
</TD>
</TR>
<TR><TD>FGFR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127273">GDB:127273</A></TD><TD>10q25.3-10q26 10q26-10q26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101600">ACROCEPHALOSYNDACTYLY TYPE V</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176943">FIBROBLAST GROWTH FACTOR RECEPTOR-2; FGFR2</A><BR>
</TD>
</TR>
<TR><TD>HK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120044">GDB:120044</A></TD><TD>10q22-10q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142600">HEXOKINASE-1; HK1</A><BR>
</TD>
</TR>
<TR><TD>HPS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127359">GDB:127359</A></TD><TD>10q23.1-10q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203300">HERMANSKY-PUDLAK SYNDROME; HPS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604982"></A><BR>
</TD>
</TR>
<TR><TD>IL2RA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119345">GDB:119345</A></TD><TD>10p15-10p14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147730">INTERLEUKIN-2 RECEPTOR, ALPHA; IL2RA</A><BR>
</TD>
</TR>
<TR><TD>LGI1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864936">GDB:9864936</A></TD><TD>10q24-10q24 10q23.33-10q23.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600512">EPILEPSY, PARTIAL; EPT</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604619"></A><BR>
</TD>
</TR>
<TR><TD>LIPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120153">GDB:120153</A></TD><TD>10q24-10q25 10q23.2-10q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278000">WOLMAN DISEASE</A><BR>
</TD>
</TR>
<TR><TD>MAT1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129077">GDB:129077</A></TD><TD>10q-10q 10q22-10q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250850">METHIONINE ADENOSYLTRANSFERASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>MBL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120167">GDB:120167</A></TD><TD>10q11.2-10q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154545">MANNOSE-BINDING PROTEIN, SERUM; MBP1</A><BR>
</TD>
</TR>
<TR><TD>MKI67</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120185">GDB:120185</A></TD><TD>10q25-10qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176741">PROLIFERATION-RELATED Ki-67 ANTIGEN; MKI67</A><BR>
</TD>
</TR>
<TR><TD>MXI1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:137182">GDB:137182</A></TD><TD>10q25-10q25 10q24-10q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600020">MAX INTERACTING PROTEIN 1; MXI1</A><BR>
</TD>
</TR>
<TR><TD>NODAL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9848762">GDB:9848762</A></TD><TD>10q22.1-10q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601265">NODAL, MOUSE, HOMOLOG OF</A><BR>
</TD>
</TR>
<TR><TD>OAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120246">GDB:120246</A></TD><TD>10q26-10q26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=258870">ORNITHINE AMINOTRANSFERASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>OATL3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:215803">GDB:215803</A></TD><TD>10q26-10q26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=258870">ORNITHINE AMINOTRANSFERASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>PAX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138771">GDB:138771</A></TD><TD>10q24-10q24 10q25-10q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167409">PAIRED BOX HOMEOTIC GENE 2; PAX2</A><BR>
</TD>
</TR>
<TR><TD>PCBD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138478">GDB:138478</A></TD><TD>10q22-10q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126090">PTERIN-4-ALPHA-CARBINOLAMINE DEHYDRATASE; PCBD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264070">PRIMAPTERINURIA</A><BR>
</TD>
</TR>
<TR><TD>PEO1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:632784">GDB:632784</A></TD><TD>10q24-10q24 10q23.3-10q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157640">PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; PEO</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606075"></A><BR>
</TD>
</TR>
<TR><TD>PHYH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9263423">GDB:9263423</A></TD><TD>10p15.3-10p12.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266500">REFSUM DISEASE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602026">PHYTANOYL-CoA HYDROXYLASE; PHYH</A><BR>
</TD>
</TR>
<TR><TD>PNLIP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127916">GDB:127916</A></TD><TD>10q24-10q26 10q26.1-10q26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=246600">LIPASE, CONGENITAL ABSENCE OF PANCREATIC</A><BR>
</TD>
</TR>
<TR><TD>PSAP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120366">GDB:120366</A></TD><TD>10q21-10q22 10q22.1-10q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176801">PROSAPOSIN; PSAP</A><BR>
</TD>
</TR>
<TR><TD>PTEN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6022948">GDB:6022948</A></TD><TD>10q23-10q23 10q23.3-10q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114500">CANCER OF COLON</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153480">MACROCEPHALY, MULTIPLE LIPOMAS AND HEMANGIOMATA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158350">MULTIPLE HAMARTOMA SYNDROME; MHAM</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=174900">POLYPOSIS, JUVENILE INTESTINAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601728">PHOSPHATASE AND TENSIN HOMOLOG; PTEN</A><BR>
</TD>
</TR>
<TR><TD>RBP4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120342">GDB:120342</A></TD><TD>10q23-10q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180250">RETINOL-BINDING PROTEIN, PLASMA; RBP4</A><BR>
</TD>
</TR>
<TR><TD>RDPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954445">GDB:9954445</A></TD><TD>10pter-10p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600964">REFSUM DISEASE WITH INCREASED PIPECOLICACIDEMIA; RDPA</A><BR>
</TD>
</TR>
<TR><TD>RET</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120346">GDB:120346</A></TD><TD>10q11.2-10q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164761">RET PROTO-ONCOGENE; RET</A><BR>
</TD>
</TR>
<TR><TD>SFTPA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119593">GDB:119593</A></TD><TD>10q22-10q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=178630">PULMONARY SURFACTANT APOPROTEIN PSP-A; PSAP</A><BR>
</TD>
</TR>
<TR><TD>SFTPD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132674">GDB:132674</A></TD><TD>10q22.2-10q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=178635">PULMONARY SURFACTANT APOPROTEIN PSP-D; PSP-D</A><BR>
</TD>
</TR>
<TR><TD>SHFM3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:386030">GDB:386030</A></TD><TD>10q24-10q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600095">SPLIT-HAND/FOOT MALFORMATION, TYPE 3; SHFM3</A><BR>
</TD>
</TR>
<TR><TD>SIAL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6549924">GDB:6549924</A></TD><TD>10pter-10q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256550">NEURAMINIDASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>THC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10794765">GDB:10794765</A></TD><TD>10p12-10p11.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188000">THROMBOCYTOPENIA</A><BR>
</TD>
</TR>
<TR><TD>TLX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119607">GDB:119607</A></TD><TD>10q24-10q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186770">HOMEO BOX-11; HOX11</A><BR>
</TD>
</TR>
<TR><TD>TNFRSF6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132671">GDB:132671</A></TD><TD>10q24.1-10q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134637">APOPTOSIS ANTIGEN 1; APT1</A><BR>
</TD>
</TR>
<TR><TD>UFS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6380714">GDB:6380714</A></TD><TD>10q23-10q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=236730">UROFACIAL SYNDROME; UFS</A><BR>
</TD>
</TR>
<TR><TD>UROS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128112">GDB:128112</A></TD><TD>10q25.2-10q26.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=263700">PORPHYRIA, CONGENITAL ERYTHROPOIETIC; CEP</A><BR>
</TD>
</TR>
<TR><TD>AA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:568984">GDB:568984</A></TD><TD>11p15-11p15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108985">ATROPHIA AREATA; AA</A><BR>
</TD>
</TR>
<TR><TD>ABCC8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:591370">GDB:591370</A></TD><TD>11p15.1-11p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600509">SULFONYLUREA RECEPTOR; SUR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601820">PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY</A><BR>
</TD>
</TR>
<TR><TD>ACAT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126861">GDB:126861</A></TD><TD>11q22.3-11q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203750">ALPHA-METHYLACETOACETICACIDURIA</A><BR>
</TD>
</TR>
<TR><TD>ALX4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10450304">GDB:10450304</A></TD><TD>11p11.2-11p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168500">PARIETAL FORAMINA, SYMMETRIC; PFM</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605420"></A><BR>
</TD>
</TR>
<TR><TD>AMPD3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136013">GDB:136013</A></TD><TD>11p15-11p15 11pter-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=102772">ADENOSINE MONOPHOSPHATE DEAMINASE-3; AMPD3</A><BR>
</TD>
</TR>
<TR><TD>ANC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954484">GDB:9954484</A></TD><TD>11q22-11qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105580">CANAL CARCINOMA</A><BR>
</TD>
</TR>
<TR><TD>APOA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119684">GDB:119684</A></TD><TD>11q23.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105200">AMYLOIDOSIS, FAMILIAL VISCERAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107680">APOLIPOPROTEIN A-I OF HIGH DENSITY LIPOPROTEIN; APOA1</A><BR>
</TD>
</TR>
<TR><TD>APOA4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119000">GDB:119000</A></TD><TD>11q23-11q23 11q23-11qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107690">APOLIPOPROTEIN A-IV; APOA4</A><BR>
</TD>
</TR>
<TR><TD>APOC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119001">GDB:119001</A></TD><TD>11q23.1-11q23.2 11q23.2-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107720">APOLIPOPROTEIN C-III; APOC3</A><BR>
</TD>
</TR>
<TR><TD>ATM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:593364">GDB:593364</A></TD><TD>11q22-11q23 11q22.3-11q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=208900">ATAXIA-TELANGIECTASIA; AT</A><BR>
</TD>
</TR>
<TR><TD>BSCL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9963996">GDB:9963996</A></TD><TD>11q13.1-11q13.5 11q13.1-11q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=269700">SEIP SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606158"></A><BR>
</TD>
</TR>
<TR><TD>BWS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120567">GDB:120567</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130650">BECKWITH-WIEDEMANN SYNDROME; BWS</A><BR>
</TD>
</TR>
<TR><TD>CALCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120571">GDB:120571</A></TD><TD>11p15.2-11p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114130">CALCITONIN/CALCITONIN-RELATED POLYPEPTIDE, ALPHA; CALCA</A><BR>
</TD>
</TR>
<TR><TD>CAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119049">GDB:119049</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115500">CATALASE; CAT</A><BR>
</TD>
</TR>
<TR><TD>CCND1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128222">GDB:128222</A></TD><TD>11q13.1-11q13.1 11q13.3-11q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151400">LEUKEMIA, CHRONIC LYMPHATIC; CLL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168461">CYCLIN D1; CCND1</A><BR>
</TD>
</TR>
<TR><TD>CD3E</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119764">GDB:119764</A></TD><TD>11q23-11q23 11q23.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186830">CD3E ANTIGEN, EPSILON POLYPEPTIDE; CD3E</A><BR>
</TD>
</TR>
<TR><TD>CD3G</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119765">GDB:119765</A></TD><TD>11q23-11q23 11q23.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186740">T3 T-CELL ANTIGEN, GAMMA CHAIN; T3G; CD3G</A><BR>
</TD>
</TR>
<TR><TD>CD59</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119769">GDB:119769</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107271">CD59 ANTIGEN P18-20; CD59</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143065">HUMAN LEUKOCYTE ANTIGEN MIC11; MIC11</A><BR>
</TD>
</TR>
<TR><TD>CDKN1C</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:593296">GDB:593296</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600856">CYCLIN-DEPENDENT KINASE INHIBITOR 1C; CDKN1C</A><BR>
</TD>
</TR>
<TR><TD>CLN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125228">GDB:125228</A></TD><TD>11p15-11p15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204500">CEROID-LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2</A><BR>
</TD>
</TR>
<TR><TD>CNTF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125919">GDB:125919</A></TD><TD>11q12-11q12 11q12.2-11q12.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118945">CILIARY NEUROTROPHIC FACTOR; CNTF</A><BR>
</TD>
</TR>
<TR><TD>CPT1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:597642">GDB:597642</A></TD><TD>11q-11q 11q13.1-11q13.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=255120">HYPOGLYCEMIA, HYPOKETOTIC, WITH DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600528">CARNITINE PALMITOYLTRANSFERASE I, LIVER; CPT1A</A><BR>
</TD>
</TR>
<TR><TD>CTSC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:642234">GDB:642234</A></TD><TD>11q14.1-11q14.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245000">KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245010">KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA AND ONYCHOGRYPOSIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602365">CATHEPSIN C; CTSC</A><BR>
</TD>
</TR>
<TR><TD>DDB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:595014">GDB:595014</A></TD><TD>11q12-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600045">DNA DAMAGE-BINDING PROTEIN; DDB1</A><BR>
</TD>
</TR>
<TR><TD>DDB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:595015">GDB:595015</A></TD><TD>11p12-11p11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600811">DNA DAMAGE-BINDING PROTEIN-2; DDB2</A><BR>
</TD>
</TR>
<TR><TD>DHCR7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9835302">GDB:9835302</A></TD><TD>11q13.2-11q13.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=270400">SMITH-LEMLI-OPITZ SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602858"></A><BR>
</TD>
</TR>
<TR><TD>DLAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118785">GDB:118785</A></TD><TD>11q23.1-11q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109720">CIRRHOSIS, PRIMARY; PBC</A><BR>
</TD>
</TR>
<TR><TD>DRD4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127782">GDB:127782</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126452">DOPAMINE RECEPTOR D4; DRD4</A><BR>
</TD>
</TR>
<TR><TD>ECB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958955">GDB:9958955</A></TD><TD>11q23-11q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=263400">POLYCYTHEMIA, BENIGN FAMILIAL</A><BR>
</TD>
</TR>
<TR><TD>ED4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9837373">GDB:9837373</A></TD><TD>11q23-11q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=225060">DYSPLASIA, MARGARITA TYPE</A><BR>
</TD>
</TR>
<TR><TD>EVR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134029">GDB:134029</A></TD><TD>11q13-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133780">EXUDATIVE VITREORETINOPATHY, FAMILIAL; EVR</A><BR>
</TD>
</TR>
<TR><TD>EXT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:344921">GDB:344921</A></TD><TD>11p12-11p11 11p12-11q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133701">EXOSTOSES, MULTIPLE, TYPE II; EXT2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215300">CHONDROSARCOMA</A><BR>
</TD>
</TR>
<TR><TD>F2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119894">GDB:119894</A></TD><TD>11p11-11q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176930">COAGULATION FACTOR II; F2</A><BR>
</TD>
</TR>
<TR><TD>FSHB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119955">GDB:119955</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136530">FOLLICLE-STIMULATING HORMONE, BETA POLYPEPTIDE; FSHB</A><BR>
</TD>
</TR>
<TR><TD>FTH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120617">GDB:120617</A></TD><TD>11q13-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134770">FERRITIN HEAVY CHAIN 1; FTH1</A><BR>
</TD>
</TR>
<TR><TD>G6PT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9862966">GDB:9862966</A></TD><TD>11q23-11q23 11q23.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232220">GLYCOGEN STORAGE DISEASE Ib</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602671"></A><BR>
</TD>
</TR>
<TR><TD>G6PT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9862967">GDB:9862967</A></TD><TD>11q23.3-11q24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232240">STORAGE DISEASE Ic</A><BR>
</TD>
</TR>
<TR><TD>GIF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118800">GDB:118800</A></TD><TD>11q12-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261000">PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR</A><BR>
</TD>
</TR>
<TR><TD>HBB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119297">GDB:119297</A></TD><TD>11p15.4-11p15.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900">HEMOGLOBIN--BETA LOCUS; HBB</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603903"></A><BR>
</TD>
</TR>
<TR><TD>HBBP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120035">GDB:120035</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141900">HEMOGLOBIN--BETA LOCUS; HBB</A><BR>
</TD>
</TR>
<TR><TD>HBD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119298">GDB:119298</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142000">HEMOGLOBIN--DELTA LOCUS; HBD</A><BR>
</TD>
</TR>
<TR><TD>HBE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119299">GDB:119299</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142100">HEMOGLOBIN--EPSILON LOCUS; HBE1</A><BR>
</TD>
</TR>
<TR><TD>HBG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119300">GDB:119300</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142200">HEMOGLOBIN, GAMMA A; HBG1</A><BR>
</TD>
</TR>
<TR><TD>HBG2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119301">GDB:119301</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142250">HEMOGLOBIN, GAMMA G; HBG2</A><BR>
</TD>
</TR>
<TR><TD>HMBS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120528">GDB:120528</A></TD><TD>11q23.3-11q23.3 11q22.3-11q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176000">PORPHYRIA, ACUTE INTERMITTENT; AIP</A><BR>
</TD>
</TR>
<TR><TD>HND</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954478">GDB:9954478</A></TD><TD>11q13-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=234500">HARTNUP DISORDER</A><BR>
</TD>
</TR>
<TR><TD>HOMG2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956484">GDB:9956484</A></TD><TD>11q23-11q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154020">MAGNESIUM WASTING, RENAL</A><BR>
</TD>
</TR>
<TR><TD>HRAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120684">GDB:120684</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109800">BLADDER CANCER</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190020">V-HA-RAS HARVEY RAT SARCOMA VIRAL ONCOGENE HOMOLOG; HRAS</A><BR>
</TD>
</TR>
<TR><TD>HVBS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120069">GDB:120069</A></TD><TD>11p14-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114550">CANCER, HEPATOCELLULAR</A><BR>
</TD>
</TR>
<TR><TD>IDDM2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128530">GDB:128530</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125852">DIABETES MELLITUS, INSULIN-DEPENDENT, 2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222100">DIABETES MELLITUS, JUVENILE-ONSET INSULIN-DEPENDENT; IDDM</A><BR>
</TD>
</TR>
<TR><TD>IGER</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119696">GDB:119696</A></TD><TD>11q12-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147050">IgE RESPONSIVENESS, ATOPIC; IGER</A><BR>
</TD>
</TR>
<TR><TD>INS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119349">GDB:119349</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176730">INSULIN; INS</A><BR>
</TD>
</TR>
<TR><TD>JBS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120111">GDB:120111</A></TD><TD>11q24.1-11q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147791">JACOBSEN SYNDROME; JBS</A><BR>
</TD>
</TR>
<TR><TD>KCNJ11</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:7009893">GDB:7009893</A></TD><TD>11p15.1-11p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600937">POTASSIUM CHANNEL, INWARDLY-RECTIFYING, SUBFAMILY J, MEMBER 11; KCNJ11</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601820">PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY</A><BR>
</TD>
</TR>
<TR><TD>KCNJ1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:204206">GDB:204206</A></TD><TD>11q24-11q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600359">POTASSIUM CHANNEL, INWARDLY-RECTIFYING, SUBFAMILY J, MEMBER 1; KCNJ1</A><BR>
</TD>
</TR>
<TR><TD>KCNQ1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:741244">GDB:741244</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=192500">LONG QT SYNDROME, TYPE 1; LQT1</A><BR>
</TD>
</TR>
<TR><TD>LDHA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120141">GDB:120141</A></TD><TD>11p15.1-11p15.1 11p15.4-11p15.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150000">LACTATE DEHYDROGENASE-A; LDHA</A><BR>
</TD>
</TR>
<TR><TD>LRP5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9836818">GDB:9836818</A></TD><TD>11q13.4-11q13.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=259770">OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601884">HIGH BONE MASS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603506"></A><BR>
</TD>
</TR>
<TR><TD>MEN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120173">GDB:120173</A></TD><TD>11q13-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131100">MULTIPLE ENDOCRINE NEOPLASIA, TYPE 1; MEN1</A><BR>
</TD>
</TR>
<TR><TD>MLL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128819">GDB:128819</A></TD><TD>11q23-11q23 11q23.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159555">MYELOID/LYMPHOID OR MIXED-LINEAGE LEUKEMIA; MLL</A><BR>
</TD>
</TR>
<TR><TD>MYBPC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:579615">GDB:579615</A></TD><TD>11p11.2-11p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115197">CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600958">MYOSIN-BINDING PROTEIN C, CARDIAC; MYBPC3</A><BR>
</TD>
</TR>
<TR><TD>MYO7A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132543">GDB:132543</A></TD><TD>11q13.5-11q13.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276903">MYOSIN VIIA; MYO7A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600060">DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 2; DFNB2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601317">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 11; DFNA11</A><BR>
</TD>
</TR>
<TR><TD>NNO1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10450513">GDB:10450513</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600165">SIMPLE, AUTOSOMAL DOMINANT</A><BR>
</TD>
</TR>
<TR><TD>OPPG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3789438">GDB:3789438</A></TD><TD>11q12-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=259770">OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG</A><BR>
</TD>
</TR>
<TR><TD>OPTB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954474">GDB:9954474</A></TD><TD>11q12-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=259700">OSTEOPETROSIS, AUTOSOMAL RECESSIVE</A><BR>
</TD>
</TR>
<TR><TD>PAX6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118997">GDB:118997</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106210">PAIRED BOX HOMEOTIC GENE 6; PAX6</A><BR>
</TD>
</TR>
<TR><TD>PC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119472">GDB:119472</A></TD><TD>11q11-11q13.1 11q13-11q13 11q13.4-11q13.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266150">PYRUVATE CARBOXYLASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>PDX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9836634">GDB:9836634</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245349">PYRUVATE DEHYDROGENASE COMPLEX, COMPONENT X</A><BR>
</TD>
</TR>
<TR><TD>PGL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:511177">GDB:511177</A></TD><TD>11q13.1-11q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601650">PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 2; PGL2</A><BR>
</TD>
</TR>
<TR><TD>PGR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119493">GDB:119493</A></TD><TD>11q22.1-11q22.3 11q22.2-11q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264080">PROGESTERONE RESISTANCE</A><BR>
</TD>
</TR>
<TR><TD>PORC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128610">GDB:128610</A></TD><TD>11q23.1-11q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176010">PORPHYRIA, CHESTER TYPE; PORC</A><BR>
</TD>
</TR>
<TR><TD>PTH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119522">GDB:119522</A></TD><TD>11p15.2-11p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168450">PARATHYROID HORMONE; PTH</A><BR>
</TD>
</TR>
<TR><TD>PTS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118856">GDB:118856</A></TD><TD>11q22.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261640">6-@PYRUVOYLTETRAHYDROPTERIN SYNTHASE; PTS</A><BR>
</TD>
</TR>
<TR><TD>PVRL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:583951">GDB:583951</A></TD><TD>11q23-11q24 11q23-11q23 11q23.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=225000">ECTODERMAL DYSPLASIA, CLEFT LIP AND PALATE, HAND AND FOOT DEFORMITY,</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=225060">DYSPLASIA, MARGARITA TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600644">POLIOVIRUS RECEPTOR RELATED; PVRR</A><BR>
</TD>
</TR>
<TR><TD>PYGM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120329">GDB:120329</A></TD><TD>11q13.1-11q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232600">GLYCOGEN STORAGE DISEASE V</A><BR>
</TD>
</TR>
<TR><TD>RAG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120334">GDB:120334</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179615">RECOMBINATION ACTIVATING GENE-1; RAG1</A><BR>
</TD>
</TR>
<TR><TD>RAG2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125186">GDB:125186</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179616">RECOMBINATION ACTIVATING GENE-2; RAG2</A><BR>
</TD>
</TR>
<TR><TD>ROM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120350">GDB:120350</A></TD><TD>11q13-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180721">ROD OUTER SEGMENT PROTEIN-1; ROM1</A><BR>
</TD>
</TR>
<TR><TD>RRAS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5573831">GDB:5573831</A></TD><TD>11p15.2-11p15.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600098">ONCOGENE TC21</A><BR>
</TD>
</TR>
<TR><TD>SAA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120364">GDB:120364</A></TD><TD>11p15.1-11p14 11p15.1-11p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104750">SERUM AMYLOID A1; SAA1</A><BR>
</TD>
</TR>
<TR><TD>SCA5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:378219">GDB:378219</A></TD><TD>11p12-11q12 11q13.1-11q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600224">SPINOCEREBELLAR ATAXIA 5; SCA5</A><BR>
</TD>
</TR>
<TR><TD>SCZD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118874">GDB:118874</A></TD><TD>11q14-11q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181500">DISORDER-2; SCZD2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603342"></A><BR>
</TD>
</TR>
<TR><TD>SDHD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132456">GDB:132456</A></TD><TD>11q23-11q23 11q22-11q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168000">PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 1; PGL1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602690"></A><BR>
</TD>
</TR>
<TR><TD>SERPING1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119041">GDB:119041</A></TD><TD>11q12.1-11q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106100">ANGIONEUROTIC EDEMA, HEREDITARY; HANE</A><BR>
</TD>
</TR>
<TR><TD>SMPD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128144">GDB:128144</A></TD><TD>11p15.3-11p15.3 11p15.4-11p15.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=257200">NIEMANN-PICK DISEASE</A><BR>
</TD>
</TR>
<TR><TD>TCIRG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9956269">GDB:9956269</A></TD><TD>11q13.4-11q13.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=259700">OSTEOPETROSIS, AUTOSOMAL RECESSIVE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604592"></A><BR>
</TD>
</TR>
<TR><TD>TCL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954468">GDB:9954468</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151390">LEUKEMIA, ACUTE T-CELL; ATL</A><BR>
</TD>
</TR>
<TR><TD>TECTA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6837718">GDB:6837718</A></TD><TD>11q22-11q24 11q23-11q24 11pter-11qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601543">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 8; DFNA8</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601842">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 12; DFNA12</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602574"></A><BR>
</TD>
</TR>
<TR><TD>TH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119612">GDB:119612</A></TD><TD>11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191290">TYROSINE HYDROXYLASE; TH</A><BR>
</TD>
</TR>
<TR><TD>TREH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958953">GDB:9958953</A></TD><TD>11q23.3-11q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=275360">TREHALASE</A><BR>
</TD>
</TR>
<TR><TD>TSG101</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1313414">GDB:1313414</A></TD><TD>11p15-11p15 11p15.2-11p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601387">TUMOR SUSCEPTIBILITY GENE 101; TSG101</A><BR>
</TD>
</TR>
<TR><TD>TYR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120476">GDB:120476</A></TD><TD>11q21-11q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203100">ALBINISM I</A><BR>
</TD>
</TR>
<TR><TD>USH1C</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132544">GDB:132544</A></TD><TD>11p14-11p14 11p15.2-11p14 11p15.1-11p15.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276904">USHER SYNDROME, TYPE IC; USH1C</A><BR>
</TD>
</TR>
<TR><TD>VMD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:133795">GDB:133795</A></TD><TD>11q13-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153700">VITELLIFORM MACULAR DYSTROPHY; VMD2</A><BR>
</TD>
</TR>
<TR><TD>VRNI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135662">GDB:135662</A></TD><TD>11q13-11q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193235">VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY; VRNI</A><BR>
</TD>
</TR>
<TR><TD>WT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120496">GDB:120496</A></TD><TD>11p13-11p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136680">FRASIER SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194070">WILMS TUMOR; WT1</A><BR>
</TD>
</TR>
<TR><TD>WT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118886">GDB:118886</A></TD><TD>11p15-11p15 11p15.5-11p15.5 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194071">MULTIPLE TUMOR ASSOCIATED CHROMOSOME REGION 1; MTACR1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=202300">ADRENOCORTICAL CARCINOMA, HEREDITARY; ADCC</A><BR>
</TD>
</TR>
<TR><TD>ZNF145</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230064">GDB:230064</A></TD><TD>11q23-11q23 11q23.1-11q23.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176797">PROMYELOCYTIC LEUKEMIA ZINC FINGER; PLZF</A><BR>
</TD>
</TR>
<TR><TD>A2M</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119639">GDB:119639</A></TD><TD>12p13.3-12p12.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103950">ALPHA-2-MACROGLOBULIN; A2M</A><BR>
</TD>
</TR>
<TR><TD>AAAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954498">GDB:9954498</A></TD><TD>12q13-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231550">GLUCOCORTICOID DEFICIENCY AND ACHALASIA</A><BR>
</TD>
</TR>
<TR><TD>ACADS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118959">GDB:118959</A></TD><TD>12q22-12qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201470">ACYL-CoA DEHYDROGENASE, SHORT-CHAIN; ACADS</A><BR>
</TD>
</TR>
<TR><TD>ACLS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136346">GDB:136346</A></TD><TD>12p13.3-12p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=200990">ACROCALLOSAL SYNDROME; ACLS</A><BR>
</TD>
</TR>
<TR><TD>ACVRL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230240">GDB:230240</A></TD><TD>12q11-12q14 12cen-12qter 12q13.12-12q13.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600376">OSLER-RENDU-WEBER SYNDROME 2; ORW2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601284">ACTIVIN A RECEPTOR, TYPE II-LIKE KINASE 1; ACVRL1</A><BR>
</TD>
</TR>
<TR><TD>ALDH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119668">GDB:119668</A></TD><TD>12q24.2-12q24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100650">ALDEHYDE DEHYDROGENASE-2; ALDH2</A><BR>
</TD>
</TR>
<TR><TD>AMHR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:696210">GDB:696210</A></TD><TD>12q13-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600956">ANTI-MULLERIAN HORMONE TYPE II RECEPTOR; AMHR2</A><BR>
</TD>
</TR>
<TR><TD>AOM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118998">GDB:118998</A></TD><TD>12q12-12q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108300">STICKLER SYNDROME, TYPE I; STL1</A><BR>
</TD>
</TR>
<TR><TD>AQP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:141853">GDB:141853</A></TD><TD>12q13-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107777">AQUAPORIN-2; AQP2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125800">DIABETES INSIPIDUS, RENAL TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222000">DIABETES INSIPIDUS, RENAL TYPE, AUTOSOMAL RECESSIVE</A><BR>
</TD>
</TR>
<TR><TD>ATD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:696353">GDB:696353</A></TD><TD>12p12.2-12p11.21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=208500">ASPHYXIATING THORACIC DYSTROPHY; ATD</A><BR>
</TD>
</TR>
<TR><TD>ATP2A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119717">GDB:119717</A></TD><TD>12q23-12q24.1 12q24.1-12q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108740">ATPase, Ca(2+)-TRANSPORTING, SLOW-TWITCH; ATP2A2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=124200">DARIER-WHITE DISEASE; DAR</A><BR>
</TD>
</TR>
<TR><TD>BDC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5584359">GDB:5584359</A></TD><TD>12q24-12q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113100">BRACHYDACTYLY, TYPE C; BDC</A><BR>
</TD>
</TR>
<TR><TD>C1R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119729">GDB:119729</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=216950">COMPLEMENT COMPONENT-C1r, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>CD4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119767">GDB:119767</A></TD><TD>12p12-12p12 12pter-12p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186940">T-CELL ANTIGEN T4/LEU3; CD4</A><BR>
</TD>
</TR>
<TR><TD>CDK4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:204022">GDB:204022</A></TD><TD>12q13-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123829">CYCLIN-DEPENDENT KINASE 4; CDK4</A><BR>
</TD>
</TR>
<TR><TD>CNA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:252119">GDB:252119</A></TD><TD>12q21.31-12q21.32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121400">CORNEA PLANA 1; CNA1</A><BR>
</TD>
</TR>
<TR><TD>COL2A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119063">GDB:119063</A></TD><TD>12q12-12q13.2 12q13.11-12q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108300">STICKLER SYNDROME, TYPE I; STL1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120140">COLLAGEN, TYPE II, ALPHA-1 CHAIN; COL2A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=200610">ACHONDROGENESIS, TYPE II; ACG2</A><BR>
</TD>
</TR>
<TR><TD>CYP27B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9835730">GDB:9835730</A></TD><TD>12q12-12q13 12q13.3-12q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264700">PSEUDOVITAMIN D DEFICIENCY RICKETS; PDDR</A><BR>
</TD>
</TR>
<TR><TD>DRPLA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:270336">GDB:270336</A></TD><TD>12p13.31-12p13.31 12p-12p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125370">DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY; DRPLA</A><BR>
</TD>
</TR>
<TR><TD>ENUR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:666422">GDB:666422</A></TD><TD>12q13-12q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600808">ENURESIS, NOCTURNAL, 2; ENUR2</A><BR>
</TD>
</TR>
<TR><TD>FEOM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:345037">GDB:345037</A></TD><TD>12p11.2-12q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=135700">FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL; FEOM</A><BR>
</TD>
</TR>
<TR><TD>FGF23</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10450034">GDB:10450034</A></TD><TD>12p13.3-12p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193100">VITAMIN D-RESISTANT RICKETS, AUTOSOMAL DOMINANT</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605380"></A><BR>
</TD>
</TR>
<TR><TD>FPF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9848880">GDB:9848880</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142680">PERIODIC FEVER, AUTOSOMAL DOMINANT</A><BR>
</TD>
</TR>
<TR><TD>GNB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120005">GDB:120005</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139130">GUANINE NUCLEOTIDE-BINDING PROTEIN, BETA POLYPEPTIDE-3; GNB3</A><BR>
</TD>
</TR>
<TR><TD>GNS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120006">GDB:120006</A></TD><TD>12q14-12q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252940">MUCOPOLYSACCHARIDOSIS TYPE IIID</A><BR>
</TD>
</TR>
<TR><TD>HAL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120746">GDB:120746</A></TD><TD>12q22-12q23 12q22-12q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=235800">HISTIDINEMIA</A><BR>
</TD>
</TR>
<TR><TD>HBP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:701889">GDB:701889</A></TD><TD>12q13-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=112410">BRACHYDACTYLY WITH HYPERTENSION</A><BR>
</TD>
</TR>
<TR><TD>HMGA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:362658">GDB:362658</A></TD><TD>12q15-12q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600698">HIGH MOBILITY GROUP PROTEIN ISOFORM I-C; HMGIC</A><BR>
</TD>
</TR>
<TR><TD>HMN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954508">GDB:9954508</A></TD><TD>12q24.3-12q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158590">MUSCULAR ATROPHY, ADULT SPINAL</A><BR>
</TD>
</TR>
<TR><TD>HPD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135978">GDB:135978</A></TD><TD>12q14-12qter 12q24-12qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276710">TYROSINEMIA, TYPE III</A><BR>
</TD>
</TR>
<TR><TD>IGF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120081">GDB:120081</A></TD><TD>12q22-12q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147440">INSULINLIKE GROWTH FACTOR 1; IGF1</A><BR>
</TD>
</TR>
<TR><TD>KCNA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127903">GDB:127903</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176260">POTASSIUM VOLTAGE-GATED CHANNEL, SHAKER-RELATED SUBFAMILY, MEMBER</A><BR>
</TD>
</TR>
<TR><TD>KERA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:252121">GDB:252121</A></TD><TD>12q21-12q21 12q21.31-12q21.32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217300">CORNEA PLANA 2; CNA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603288"></A><BR>
</TD>
</TR>
<TR><TD>KRAS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120120">GDB:120120</A></TD><TD>12p12.1-12p12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114500">CANCER OF COLON</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190070">V-KI-RAS2 KIRSTEN RAT SARCOMA 2 VIRAL ONCOGENE HOMOLOG; KRAS2</A><BR>
</TD>
</TR>
<TR><TD>KRT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128198">GDB:128198</A></TD><TD>12q11-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139350">KERATIN 1; KRT1</A><BR>
</TD>
</TR>
<TR><TD>KRT2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:407640">GDB:407640</A></TD><TD>12q11-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146800">ICHTHYOSIS, BULLOUS TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600194">KERATIN 2A; KRT2A</A><BR>
</TD>
</TR>
<TR><TD>KRT3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136276">GDB:136276</A></TD><TD>12q12-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148043">KERATIN 3; KRT3</A><BR>
</TD>
</TR>
<TR><TD>KRT4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120697">GDB:120697</A></TD><TD>12p12.2-12q11 12p11.2-12q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123940">KERATIN 4; KRT4</A><BR>
</TD>
</TR>
<TR><TD>KRT5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128110">GDB:128110</A></TD><TD>12q-12q 12q11-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131760">EPIDERMOLYSIS BULLOSA HERPETIFORMIS, DOWLING-MEARA TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148040">KERATIN 5; KRT5</A><BR>
</TD>
</TR>
<TR><TD>KRT6A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128111">GDB:128111</A></TD><TD>12q12-12q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148041">KERATIN 6A; KRT6A</A><BR>
</TD>
</TR>
<TR><TD>KRT6B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128113">GDB:128113</A></TD><TD>12pter-12qter 12q12-12q13.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148042">KERATIN 6B; KRT6B</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167210">PACHYONYCHIA CONGENITA, JACKSON-LAWLER TYPE</A><BR>
</TD>
</TR>
<TR><TD>KRTHB6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:702078">GDB:702078</A></TD><TD>12q13-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158000">MONILETHRIX</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601928">KERATIN, HAIR BASIC (TYPE II) 6</A><BR>
</TD>
</TR>
<TR><TD>LDHB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120147">GDB:120147</A></TD><TD>12p12.2-12p12.1 12p12.1-12p12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150100">LACTATE DEHYDROGENASE-B; LDHB</A><BR>
</TD>
</TR>
<TR><TD>LYZ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120160">GDB:120160</A></TD><TD>12pter-12qter 12q14.2-12q14.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105200">AMYLOIDOSIS, FAMILIAL VISCERAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=153450">LYSOZYME; LYZ</A><BR>
</TD>
</TR>
<TR><TD>MGCT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954504">GDB:9954504</A></TD><TD>12q22-12q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=273300">TESTICULAR TUMORS</A><BR>
</TD>
</TR>
<TR><TD>MPE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120191">GDB:120191</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131440">MALIGNANT PROLIFERATION OF</A><BR>
</TD>
</TR>
<TR><TD>MVK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134189">GDB:134189</A></TD><TD>12pter-12qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=251170">MEVALONICACIDURIA</A><BR>
</TD>
</TR>
<TR><TD>MYL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128829">GDB:128829</A></TD><TD>12q23-12q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160781">MYOSIN, LIGHT CHAIN, REGULATORY VENTRICULAR; MYL2</A><BR>
</TD>
</TR>
<TR><TD>OAP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120245">GDB:120245</A></TD><TD>12q12-12q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=165720">OSTEOARTHROSIS, PRECOCIOUS; OAP</A><BR>
</TD>
</TR>
<TR><TD>PAH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119470">GDB:119470</A></TD><TD>12q22-12q24.2 12q24.1-12q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261600">PHENYLKETONURIA; PKU1</A><BR>
</TD>
</TR>
<TR><TD>PPKB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:696352">GDB:696352</A></TD><TD>12q11-12q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600231">PALMOPLANTAR KERATODERMA, BOTHNIAN TYPE; PPKB</A><BR>
</TD>
</TR>
<TR><TD>PRB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119513">GDB:119513</A></TD><TD>12p13.2-12p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168840">PAROTID SALIVARY GLYCOPROTEIN; G1</A><BR>
</TD>
</TR>
<TR><TD>PTPN11</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:137093">GDB:137093</A></TD><TD>12q24.1-12q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=163950">NOONAN SYNDROME 1; NS1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176876">PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR TYPE, 11; PTPN11</A><BR>
</TD>
</TR>
<TR><TD>PXR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433739">GDB:433739</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214100">ZELLWEGER SYNDROME; ZS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600414">PEROXISOME RECEPTOR 1; PXR1</A><BR>
</TD>
</TR>
<TR><TD>RLS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11501392">GDB:11501392</A></TD><TD>12q13-12q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=102300">ACROMELALGIA, HEREDITARY</A><BR>
</TD>
</TR>
<TR><TD>RSN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:139158">GDB:139158</A></TD><TD>12q24.3-12q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179838">RESTIN; RSN</A><BR>
</TD>
</TR>
<TR><TD>SAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128054">GDB:128054</A></TD><TD>12q13-12q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181035">SARCOMA AMPLIFIED SEQUENCE; SAS</A><BR>
</TD>
</TR>
<TR><TD>SAX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11507787">GDB:11507787</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108600">ATAXIA, SPASTIC</A><BR>
</TD>
</TR>
<TR><TD>SCA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128034">GDB:128034</A></TD><TD>12q24-12q24 12q23-12q24.1 12q24.1-12q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=183090">SPINOCEREBELLAR ATAXIA 2; SCA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601517">ATAXIN-2; ATX2</A><BR>
</TD>
</TR>
<TR><TD>SCNN1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:366596">GDB:366596</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600228">SODIUM CHANNEL, NONVOLTAGE-GATED, 1; SCNN1A</A><BR>
</TD>
</TR>
<TR><TD>SMAL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954506">GDB:9954506</A></TD><TD>12q23-12q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600175">SPINAL MUSCULAR ATROPHY, CONGENITAL NONPROGRESSIVE, OF LOWER LIMBS</A><BR>
</TD>
</TR>
<TR><TD>SPPM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954502">GDB:9954502</A></TD><TD>12q13.3-12q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181430">SCAPULOPERONEAL MYOPATHY; SPM</A><BR>
</TD>
</TR>
<TR><TD>SPSMA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954510">GDB:9954510</A></TD><TD>12q24.1-12q24.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181405">SCAPULOPERONEAL AMYOTROPHY, NEUROGENIC, NEW ENGLAND TYPE</A><BR>
</TD>
</TR>
<TR><TD>TBX3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:681969">GDB:681969</A></TD><TD>12q23-12q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181450">ULNAR-MAMMARY SYNDROME; UMS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601621">T-BOX 3; TBX3</A><BR>
</TD>
</TR>
<TR><TD>TBX5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6175917">GDB:6175917</A></TD><TD>12q21-12qter 12q23-12q24.1 12q24.1-12q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142900">HOLT-ORAM SYNDROME; HOS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601620">T-BOX 5; TBX5</A><BR>
</TD>
</TR>
<TR><TD>TCF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125297">GDB:125297</A></TD><TD>12q24.3-12q24.3 12q24.2-12q24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142410">TRANSCRIPTION FACTOR 1, HEPATIC; TCF1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600496">MATURITY-ONSET DIABETES OF THE YOUNG, TYPE III; MODY3</A><BR>
</TD>
</TR>
<TR><TD>TPI1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119617">GDB:119617</A></TD><TD>12p13-12p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190450">TRIOSEPHOSPHATE ISOMERASE 1; TPI1</A><BR>
</TD>
</TR>
<TR><TD>TSC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127930">GDB:127930</A></TD><TD>12q22-12q24.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191091">SCLEROSIS-3; TSC3</A><BR>
</TD>
</TR>
<TR><TD>ULR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:594089">GDB:594089</A></TD><TD>12q14-12q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150699">UTERINE</A><BR>
</TD>
</TR>
<TR><TD>VDR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120487">GDB:120487</A></TD><TD>12q12-12q14 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277440">VITAMIN D-RESISTANT RICKETS WITH END-ORGAN UNRESPONSIVENESS TO 1,25-DIHYDROXYCHOLECALCIFEROL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601769">VITAMIN D RECEPTOR; VDR</A><BR>
</TD>
</TR>
<TR><TD>VWF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119125">GDB:119125</A></TD><TD>12p13.3-12p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193400">VON WILLEBRAND DISEASE; VWD</A><BR>
</TD>
</TR>
<TR><TD>ATP7B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120494">GDB:120494</A></TD><TD>13q14.3-13q21.1 13q14.3-13q14.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277900">WILSON DISEASE; WND</A><BR>
</TD>
</TR>
<TR><TD>BRCA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:387848">GDB:387848</A></TD><TD>13q12-13q13 13q12.3-13q12.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600185">BREAST CANCER 2, EARLY-ONSET; BRCA2</A><BR>
</TD>
</TR>
<TR><TD>BRCD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954522">GDB:9954522</A></TD><TD>13pter-13qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=211410">BREAST CANCER, DUCTAL, 1; BRCD1</A><BR>
</TD>
</TR>
<TR><TD>CLN5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230991">GDB:230991</A></TD><TD>13q21.2-13q32 13q22-13q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256731">CEROID-LIPOFUSCNOSIS, NEURONAL 5; CLN5</A><BR>
</TD>
</TR>
<TR><TD>CPB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129546">GDB:129546</A></TD><TD>13pter-13qter 13q14.1-13q14.1 13q14.11-13q14.11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212070">CARBOXYPEPTIDASE B2, PLASMA; CPB2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603101"></A><BR>
</TD>
</TR>
<TR><TD>ED2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9834522">GDB:9834522</A></TD><TD>13q11-13q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=129500">ECTODERMAL DYSPLASIA, HIDROTIC; HED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604418"></A><BR>
</TD>
</TR>
<TR><TD>EDNRB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129075">GDB:129075</A></TD><TD>13q22-13q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131244">ENDOTHELIN-B RECEPTOR; EDNRB</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600155">HIRSCHSPRUNG DISEASE-2; HSCR2</A><BR>
</TD>
</TR>
<TR><TD>ENUR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:594516">GDB:594516</A></TD><TD>13q13-13q14.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600631">ENURESIS, NOCTURNAL, 1; ENUR1</A><BR>
</TD>
</TR>
<TR><TD>ERCC5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120515">GDB:120515</A></TD><TD>13q32-13q32 13q33-13q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133530">EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 5; ERCC5</A><BR>
</TD>
</TR>
<TR><TD>F10</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119890">GDB:119890</A></TD><TD>13q34-13q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134530">X, QUANTITATIVE VARIATION IN</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227600">FACTOR X DEFICIENCY; F10</A><BR>
</TD>
</TR>
<TR><TD>F7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119897">GDB:119897</A></TD><TD>13q34-13q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227500">FACTOR VII DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>GJB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125247">GDB:125247</A></TD><TD>13q11-13q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121011">GAP JUNCTION PROTEIN, BETA-2, 26 KD; GJB2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=220290">DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 1; DFNB1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601544">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 3; DFNA3</A><BR>
</TD>
</TR>
<TR><TD>GJB6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958357">GDB:9958357</A></TD><TD>13q12-13q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=129500">ECTODERMAL DYSPLASIA, HIDROTIC; HED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601544">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 3; DFNA3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604418"></A><BR>
</TD>
</TR>
<TR><TD>IPF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:448899">GDB:448899</A></TD><TD>13q12.1-13q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600733">INSULIN PROMOTER FACTOR 1; IPF1</A><BR>
</TD>
</TR>
<TR><TD>MBS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128365">GDB:128365</A></TD><TD>13q12.2-13q12.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157900">MOEBIUS SYNDROME; MBS</A><BR>
</TD>
</TR>
<TR><TD>MCOR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954520">GDB:9954520</A></TD><TD>13q31-13q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156600">CONGENITAL</A><BR>
</TD>
</TR>
<TR><TD>NYS4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11519111">GDB:11519111</A></TD><TD>13q31-13q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=193003">DISORDER WITH PREDOMINANT OCULAR SIGNS</A><BR>
</TD>
</TR>
<TR><TD>PCCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119473">GDB:119473</A></TD><TD>13q32-13q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232000">GLYCINEMIA, KETOTIC, I</A><BR>
</TD>
</TR>
<TR><TD>RB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118734">GDB:118734</A></TD><TD>13q14.12-13q14.2 13q14.2-13q14.2 13q14.3-13q14.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109800">BLADDER CANCER</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180200">RETINOBLASTOMA; RB1</A><BR>
</TD>
</TR>
<TR><TD>RHOK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:371598">GDB:371598</A></TD><TD>13q34-13q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180381">RHODOPSIN KINASE; RHOK</A><BR>
</TD>
</TR>
<TR><TD>SCZD7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864734">GDB:9864734</A></TD><TD>13q32-13q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=181500">DISORDER-2; SCZD2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603176"></A><BR>
</TD>
</TR>
<TR><TD>SGCG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3763329">GDB:3763329</A></TD><TD>13q12-13q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253700">MUSCULAR DYSTROPHY, LIMB GIRDLE, TYPE 2C; LGMD2C</A><BR>
</TD>
</TR>
<TR><TD>SLC10A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:677534">GDB:677534</A></TD><TD>13q33-13q33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601295">SOLUTE CARRIER FAMILY 10, MEMBER 2; SLC10A2</A><BR>
</TD>
</TR>
<TR><TD>SLC25A15</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120042">GDB:120042</A></TD><TD>13q34-13q34 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238970">HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603861"></A><BR>
</TD>
</TR>
<TR><TD>STARP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:635459">GDB:635459</A></TD><TD>13pter-13qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600617">STEROIDOGENIC ACUTE REGULATORY PROTEIN; STAR</A><BR>
</TD>
</TR>
<TR><TD>ZNF198</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6382650">GDB:6382650</A></TD><TD>13q11-13q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602221">ZINC FINGER PROTEIN-198; ZNF198</A><BR>
</TD>
</TR>
<TR><TD>ACHM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132458">GDB:132458</A></TD><TD>14pter-14qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=216900">COLORBLINDNESS, TOTAL</A><BR>
</TD>
</TR>
<TR><TD>ARVD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:371339">GDB:371339</A></TD><TD>14q23-14q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107970">ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1</A><BR>
</TD>
</TR>
<TR><TD>BCH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118758">GDB:118758</A></TD><TD>14q13.1-14q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118700">CHOREA, HEREDITARY BENIGN; BCH</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600635">THYROID TRANSCRIPTION FACTOR 1; TITF1</A><BR>
</TD>
</TR>
<TR><TD>CTAA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265299">GDB:265299</A></TD><TD>14q24-14qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115650">CATARACT, ANTERIOR POLAR 1; CTAA1</A><BR>
</TD>
</TR>
<TR><TD>DAD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:407505">GDB:407505</A></TD><TD>14q11-14q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600243">DEFENDER AGAINST CELL DEATH; DAD1</A><BR>
</TD>
</TR>
<TR><TD>DFNB5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:636176">GDB:636176</A></TD><TD>14q12-14q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600792">DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 5; DFNB5</A><BR>
</TD>
</TR>
<TR><TD>EML1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6328385">GDB:6328385</A></TD><TD>14q32-14q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276900">USHER SYNDROME, TYPE IA; USH1A</A><BR>
</TD>
</TR>
<TR><TD>GALC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119970">GDB:119970</A></TD><TD>14q31-14q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245200">KRABBE DISEASE</A><BR>
</TD>
</TR>
<TR><TD>GCH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118798">GDB:118798</A></TD><TD>14q22.1-14q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=128230">DYSTONIA, PROGRESSIVE, WITH DIURNAL VARIATION</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=233910">GTP CYCLOHYDROLASE I DEFICIENCY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600225">GTP CYCLOHYDROLASE I; GCH1</A><BR>
</TD>
</TR>
<TR><TD>IBGC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10450404">GDB:10450404</A></TD><TD>14q12-14q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=213600">CEREBRAL CALCIFICATION, NONARTERIOSCLEROTIC</A><BR>
</TD>
</TR>
<TR><TD>IGH@</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118731">GDB:118731</A></TD><TD>14q32.33-14q32.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146900">IgA CONSTANT HEAVY CHAIN 1; IGHA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146910">IMMUNOGLOBULIN: D (DIVERSITY) REGION OF HEAVY CHAIN</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147000">IgA CONSTANT HEAVY CHAIN 2; IGHA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147010">IMMUNOGLOBULIN: J (JOINING) LOCI OF HEAVY CHAIN; IGHJ</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147020">IMMUNOGLOBULIN: HEAVY Mu CHAIN; Mu1; IGHM1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147070">IMMUNOGLOBULIN: VARIABLE REGION OF HEAVY CHAINS--Hv1; IGHV</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147100">IgG HEAVY CHAIN LOCUS; IGHG1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147110">IMMUNOGLOBULIN Gm-2; IGHG2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147120">IMMUNOGLOBULIN Gm-3; IGHG3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147130">IMMUNOGLOBULIN Gm-4; IGHG4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147170">IMMUNOGLOBULIN: HEAVY DELTA CHAIN; IGHD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147180">IMMUNOGLOBULIN: HEAVY EPSILON CHAIN; IGHE</A><BR>
</TD>
</TR>
<TR><TD>IGHC group</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9992632">GDB:9992632</A></TD><TD>14q32.33-14q32.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146900">IgA CONSTANT HEAVY CHAIN 1; IGHA1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147000">IgA CONSTANT HEAVY CHAIN 2; IGHA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147020">IMMUNOGLOBULIN: HEAVY Mu CHAIN; Mu1; IGHM1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147100">IgG HEAVY CHAIN LOCUS; IGHG1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147110">IMMUNOGLOBULIN Gm-2; IGHG2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147120">IMMUNOGLOBULIN Gm-3; IGHG3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147130">IMMUNOGLOBULIN Gm-4; IGHG4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147170">IMMUNOGLOBULIN: HEAVY DELTA CHAIN; IGHD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147180">IMMUNOGLOBULIN: HEAVY EPSILON CHAIN; IGHE</A><BR>
</TD>
</TR>
<TR><TD>IGHG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120085">GDB:120085</A></TD><TD>14q32.33-14q32.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147100">IgG HEAVY CHAIN LOCUS; IGHG1</A><BR>
</TD>
</TR>
<TR><TD>IGHM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120086">GDB:120086</A></TD><TD>14q32.33-14q32.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147020">IMMUNOGLOBULIN: HEAVY Mu CHAIN; Mu1; IGHM1</A><BR>
</TD>
</TR>
<TR><TD>IGHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954529">GDB:9954529</A></TD><TD>14q32.33-14q32.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=144120">G1(A1) SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>IV</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:139274">GDB:139274</A></TD><TD>14q32-14q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=270100">INVERSUS VISCERUM</A><BR>
</TD>
</TR>
<TR><TD>LTBP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:453890">GDB:453890</A></TD><TD>14q24-14q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602091">LATENT TRANSFORMING GROWTH FACTOR-BETA BINDING PROTEIN 2; LTBP2</A><BR>
</TD>
</TR>
<TR><TD>MCOP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954527">GDB:9954527</A></TD><TD>14q32-14q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=251600">MICROPHTHALMOS</A><BR>
</TD>
</TR>
<TR><TD>MJD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118840">GDB:118840</A></TD><TD>14q21-14q21 14q32.1-14q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109150">MACHADO-JOSEPH DISEASE; MJD</A><BR>
</TD>
</TR>
<TR><TD>MNG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6540062">GDB:6540062</A></TD><TD>14q-14q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138800">GOITER, MULTINODULAR 1; MNG1</A><BR>
</TD>
</TR>
<TR><TD>MPD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230271">GDB:230271</A></TD><TD>14q11-14q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160500">MYOPATHY, LATE DISTAL HEREDITARY</A><BR>
</TD>
</TR>
<TR><TD>MPS3C</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954532">GDB:9954532</A></TD><TD>14pter-14qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252930">MUCOPOLYSACCHARIDOSIS TYPE IIIC</A><BR>
</TD>
</TR>
<TR><TD>MYH6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120214">GDB:120214</A></TD><TD>14q11.2-14q13 14q12-14q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160710">MYOSIN, HEAVY POLYPEPTIDE 6; MYH6</A><BR>
</TD>
</TR>
<TR><TD>MYH7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120215">GDB:120215</A></TD><TD>14q11.2-14q12 14q12-14q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160760">MYOSIN, CARDIAC, HEAVY CHAIN, BETA; MYH7</A><BR>
</TD>
</TR>
<TR><TD>NP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120239">GDB:120239</A></TD><TD>14q11.2-14q11.2 14q13.1-14q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164050">NUCLEOSIDE PHOSPHORYLASE; NP</A><BR>
</TD>
</TR>
<TR><TD>NPC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957680">GDB:9957680</A></TD><TD>14q24.3-14q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601015">MALFORMATIONS, MULTIPLE, WITH LIMB ABNORMALITIES AND HYPOPITUITARISM</A><BR>
</TD>
</TR>
<TR><TD>PABPN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:567135">GDB:567135</A></TD><TD>14q11.2-14q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164300">OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=257950">OCULOPHARYNGEAL MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602279">POLYADENYLATE-BINDING PROTEIN-2; PABP2</A><BR>
</TD>
</TR>
<TR><TD>PSEN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135682">GDB:135682</A></TD><TD>14q24.3-14q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104311">ALZHEIMER DISEASE, FAMILIAL, TYPE 3; AD3</A><BR>
</TD>
</TR>
<TR><TD>PYGL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120328">GDB:120328</A></TD><TD>14q21-14q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232700">GLYCOGEN STORAGE DISEASE VI</A><BR>
</TD>
</TR>
<TR><TD>RPGRIP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498766">GDB:11498766</A></TD><TD>14q11-14q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204000">AMAUROSIS CONGENITA OF LEBER I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605446"></A><BR>
</TD>
</TR>
<TR><TD>SERPINA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120289">GDB:120289</A></TD><TD>14q32.1-14q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107400">PROTEASE INHIBITOR 1; PI</A><BR>
</TD>
</TR>
<TR><TD>SERPINA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118955">GDB:118955</A></TD><TD>14q32.1-14q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107280">ALPHA-1-ANTICHYMOTRYPSIN; AACT</A><BR>
</TD>
</TR>
<TR><TD>SERPINA6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127865">GDB:127865</A></TD><TD>14q32.1-14q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122500">CORTICOSTEROID-BINDING GLOBULIN; CBG</A><BR>
</TD>
</TR>
<TR><TD>SLC7A7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9863033">GDB:9863033</A></TD><TD>14q11.2-14q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=222700">DIBASICAMINOACIDURIA II</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603593"></A><BR>
</TD>
</TR>
<TR><TD>SPG3A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230126">GDB:230126</A></TD><TD>14q12-14q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182600">SPASTIC PARAPLEGIA-3, AUTOSOMAL DOMINANT; SPG3A</A><BR>
</TD>
</TR>
<TR><TD>SPTB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119602">GDB:119602</A></TD><TD>14q23-14q23 14q22-14q23.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130600">ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166900">HEREDITARY HEMOLYTIC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182870">SPECTRIN, BETA, ERYTHROCYTIC; SPTB</A><BR>
</TD>
</TR>
<TR><TD>TCL1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250785">GDB:250785</A></TD><TD>14q32.1-14q32.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186960">T-CELL LYMPHOMA OR LEUKEMIA</A><BR>
</TD>
</TR>
<TR><TD>TGM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125299">GDB:125299</A></TD><TD>14q11.2-14q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190195">TRANSGLUTAMINASE 1; TGM1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=242300">ICHTHYOSIS CONGENITA</A><BR>
</TD>
</TR>
<TR><TD>TITF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132588">GDB:132588</A></TD><TD>14q13-14q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600635">THYROID TRANSCRIPTION FACTOR 1; TITF1</A><BR>
</TD>
</TR>
<TR><TD>TMIP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954523">GDB:9954523</A></TD><TD>14q13-14q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=135750">AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUS</A><BR>
</TD>
</TR>
<TR><TD>TRA@</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120404">GDB:120404</A></TD><TD>14q11.2-14q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186880">T-CELL ANTIGEN RECEPTOR, ALPHA SUBUNIT; TCRA</A><BR>
</TD>
</TR>
<TR><TD>TSHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125313">GDB:125313</A></TD><TD>14q31-14q31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=275200">THYROTROPIN, UNRESPONSIVENESS TO</A><BR>
</TD>
</TR>
<TR><TD>USH1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118885">GDB:118885</A></TD><TD>14q32-14q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276900">USHER SYNDROME, TYPE IA; USH1A</A><BR>
</TD>
</TR>
<TR><TD>VP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120492">GDB:120492</A></TD><TD>14q31-14q32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176200">PORPHYRIA VARIEGATA</A><BR>
</TD>
</TR>
<TR><TD>ACCPN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5457725">GDB:5457725</A></TD><TD>15q13-15q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=218000">CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY</A><BR>
</TD>
</TR>
<TR><TD>AHO2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954535">GDB:9954535</A></TD><TD>15q11-15q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103581">HEREDITARY OSTEODYSTROPHY-2; AHO2</A><BR>
</TD>
</TR>
<TR><TD>ANCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119678">GDB:119678</A></TD><TD>15q11-15q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105830">ANGELMAN SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>B2M</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119028">GDB:119028</A></TD><TD>15q21-15q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109700">BETA-2-MICROGLOBULIN; B2M</A><BR>
</TD>
</TR>
<TR><TD>BBS4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:511199">GDB:511199</A></TD><TD>15q22.3-15q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600374">BARDET-BIEDL SYNDROME, TYPE 4; BBS4</A><BR>
</TD>
</TR>
<TR><TD>BLM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135698">GDB:135698</A></TD><TD>15q26.1-15q26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114500">CANCER OF COLON</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=210900">BLOOM SYNDROME; BLM</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604610"></A><BR>
</TD>
</TR>
<TR><TD>CAPN3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119751">GDB:119751</A></TD><TD>15q15-15q15 15pter-15qter 15q15.1-15q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114240">CALPAIN, LARGE POLYPEPTIDE L3; CAPN3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253600">MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2; LGMD2</A><BR>
</TD>
</TR>
<TR><TD>CDAN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9823267">GDB:9823267</A></TD><TD>15q15.1-15q15.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=224120">DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE I</A><BR>
</TD>
</TR>
<TR><TD>CDAN3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:386192">GDB:386192</A></TD><TD>15q21-15q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105600">DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE III; CDAN3</A><BR>
</TD>
</TR>
<TR><TD>CLN6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4073043">GDB:4073043</A></TD><TD>15q21-15q21 15q21-15q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601780">CEROID-LIPOFUSCINOSIS, NEURONAL 6, LATE INFANTILE, VARIANT; CLN6</A><BR>
</TD>
</TR>
<TR><TD>CMH3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138299">GDB:138299</A></TD><TD>15q2-15q2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115196">CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3</A><BR>
</TD>
</TR>
<TR><TD>CYP19</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119830">GDB:119830</A></TD><TD>15q21-15q21 15q21.1-15q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107910">CYTOCHROME P450, SUBFAMILY XIX; CYP19</A><BR>
</TD>
</TR>
<TR><TD>CYP1A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120604">GDB:120604</A></TD><TD>15q22-15q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108330">CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 1; CYP1A1</A><BR>
</TD>
</TR>
<TR><TD>CYP1A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118780">GDB:118780</A></TD><TD>15pter-15qter 15q22-15qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=124060">CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 2; CYP1A2</A><BR>
</TD>
</TR>
<TR><TD>DYX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1391796">GDB:1391796</A></TD><TD>15q21-15q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=127700">DYSLEXIA, SPECIFIC, 1; DYX1</A><BR>
</TD>
</TR>
<TR><TD>EPB42</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127385">GDB:127385</A></TD><TD>15q15-15q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166900">HEREDITARY HEMOLYTIC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177070">PROTEIN 4.2, ERYTHROCYTIC; EPB42</A><BR>
</TD>
</TR>
<TR><TD>ETFA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119121">GDB:119121</A></TD><TD>15q23-15q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231680">GLUTARICACIDURIA IIA; GA IIA</A><BR>
</TD>
</TR>
<TR><TD>EYCL3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4590306">GDB:4590306</A></TD><TD>15q11-15q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227220">EYE COLOR-3; EYCL3</A><BR>
</TD>
</TR>
<TR><TD>FAH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119901">GDB:119901</A></TD><TD>15q23-15q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276700">TYROSINEMIA, TYPE I</A><BR>
</TD>
</TR>
<TR><TD>FBN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127115">GDB:127115</A></TD><TD>15q21.1-15q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134797">FIBRILLIN-1; FBN1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154700">MARFAN SYNDROME; MFS</A><BR>
</TD>
</TR>
<TR><TD>FES</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119906">GDB:119906</A></TD><TD>15q26.1-15q26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190030">V-FES FELINE SARCOMA VIRAL/V-FPS FUJINAMI AVIAN SARCOMA VIRAL ONCOGENE</A><BR>
</TD>
</TR>
<TR><TD>HCVS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119306">GDB:119306</A></TD><TD>15q11-15qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122460">CORONAVIRUS 229E SUSCEPTIBILITY; CVS</A><BR>
</TD>
</TR>
<TR><TD>HEXA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120040">GDB:120040</A></TD><TD>15q23-15q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=272800">TAY-SACHS DISEASE; TSD</A><BR>
</TD>
</TR>
<TR><TD>IVD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119354">GDB:119354</A></TD><TD>15q14-15q15 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=243500">ISOVALERICACIDEMIA; IVA</A><BR>
</TD>
</TR>
<TR><TD>LCS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11500552">GDB:11500552</A></TD><TD>15q-15q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214900">CHOLESTASIS-LYMPHEDEMA SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>LIPC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119366">GDB:119366</A></TD><TD>15q21-15q22 15q21-15q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151670">LIPASE, HEPATIC; LIPC</A><BR>
</TD>
</TR>
<TR><TD>MYO5A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:218824">GDB:218824</A></TD><TD>15q21-15q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160777">MYOSIN VA; MYO5A</A><BR>
</TD>
</TR>
<TR><TD>OCA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136820">GDB:136820</A></TD><TD>15q11.2-15q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203200">ALBINISM II</A><BR>
</TD>
</TR>
<TR><TD>OTSC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9860473">GDB:9860473</A></TD><TD>15q25-15q26 15q26.1-15q26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166800">OTOSCLEROSIS</A><BR>
</TD>
</TR>
<TR><TD>PWCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120325">GDB:120325</A></TD><TD>15q11-15q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176270">PRADER-WILLI SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>RLBP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127341">GDB:127341</A></TD><TD>15q26-15q26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180090">RETINALDEHYDE-BINDING PROTEIN 1,; RLBP1</A><BR>
</TD>
</TR>
<TR><TD>SLC12A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:386121">GDB:386121</A></TD><TD>15q15-15q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600839">SOLUTE CARRIER FAMILY 12, MEMBER 1; SLC12A1</A><BR>
</TD>
</TR>
<TR><TD>SPG6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:511201">GDB:511201</A></TD><TD>15q11.2-15q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600363">SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6</A><BR>
</TD>
</TR>
<TR><TD>TPM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127875">GDB:127875</A></TD><TD>15q22-15q22 15q22.1-15q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191010">TROPOMYOSIN 1; TPM1</A><BR>
</TD>
</TR>
<TR><TD>UBE3A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:228487">GDB:228487</A></TD><TD>15q11-15q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105830">ANGELMAN SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601623">UBIQUITIN-PROTEIN LIGASE E3A; UBE3A</A><BR>
</TD>
</TR>
<TR><TD>WMS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5583902">GDB:5583902</A></TD><TD>15q21.1-15q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277600">WEILL-MARCHESANI SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>ABCC6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9315106">GDB:9315106</A></TD><TD>16p13.1-16p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177850">PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL DOMINANT; PXE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264800">PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL RECESSIVE; PXE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603234"></A><BR>
</TD>
</TR>
<TR><TD>ALDOA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118993">GDB:118993</A></TD><TD>16q22.2-16q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103850">ALDOLASE A, FRUCTOSE-BISPHOSPHATE; ALDOA</A><BR>
</TD>
</TR>
<TR><TD>APRT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119003">GDB:119003</A></TD><TD>16q24.2-16qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=102600">ADENINE PHOSPHORIBOSYLTRANSFERASE; APRT</A><BR>
</TD>
</TR>
<TR><TD>ATP2A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119716">GDB:119716</A></TD><TD>16p12.1-16p12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108730">ATPase, Ca(2+)-TRANSPORTING, FAST-TWITCH 1; ATP2A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601003">BRODY MYOPATHY</A><BR>
</TD>
</TR>
<TR><TD>BBS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:229992">GDB:229992</A></TD><TD>16q21-16q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=209900">BARDET-BIEDL SYNDROME, TYPE 2; BBS2</A><BR>
</TD>
</TR>
<TR><TD>CARD15</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11026232">GDB:11026232</A></TD><TD>16q12-16q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186580">SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266600">REGIONAL ENTERITIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605956"></A><BR>
</TD>
</TR>
<TR><TD>CATM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:701219">GDB:701219</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156850">MICROPHTHALMIA-CATARACT</A><BR>
</TD>
</TR>
<TR><TD>CDH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120484">GDB:120484</A></TD><TD>16q22.1-16q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=192090">CADHERIN 1; CDH1</A><BR>
</TD>
</TR>
<TR><TD>CETP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119773">GDB:119773</A></TD><TD>16q21-16q21 16q13-16q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118470">CHOLESTERYL ESTER TRANSFER PROTEIN, PLASMA; CETP</A><BR>
</TD>
</TR>
<TR><TD>CHST6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131407">GDB:131407</A></TD><TD>16q22-16q22 16q22.1-16q23.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217800">CORNEAL DYSTROPHY, MACULAR TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605294"></A><BR>
</TD>
</TR>
<TR><TD>CLN3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120593">GDB:120593</A></TD><TD>16p12.1-16p12.1 16p12.1-16p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204200">CEROID-LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3</A><BR>
</TD>
</TR>
<TR><TD>CREBBP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:437159">GDB:437159</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180849">RUBINSTEIN SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600140">CREB-BINDING PROTEIN; CREBBP</A><BR>
</TD>
</TR>
<TR><TD>CTH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119086">GDB:119086</A></TD><TD>16pter-16qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=219500">CYSTATHIONINURIA</A><BR>
</TD>
</TR>
<TR><TD>CTM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119819">GDB:119819</A></TD><TD>16q22.1-16q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=116800">CATARACT, ZONULAR</A><BR>
</TD>
</TR>
<TR><TD>CYBA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125238">GDB:125238</A></TD><TD>16q24-16q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=233690">GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-NEGATIVE FORM</A><BR>
</TD>
</TR>
<TR><TD>CYLD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:701216">GDB:701216</A></TD><TD>16q12-16q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=132700">EPITHELIOMA, HEREDITARY MULTIPLE BENIGN CYSTIC</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605018"></A><BR>
</TD>
</TR>
<TR><TD>DHS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958268">GDB:9958268</A></TD><TD>16q23-16q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194380">XEROCYTOSIS, HEREDITARY</A><BR>
</TD>
</TR>
<TR><TD>DNASE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132846">GDB:132846</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125505">DEOXYRIBONUCLEASE I; DNASE1</A><BR>
</TD>
</TR>
<TR><TD>DPEP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128059">GDB:128059</A></TD><TD>16q24-16q24 16q24.3-16q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179780">RENAL DIPEPTIDASE</A><BR>
</TD>
</TR>
<TR><TD>ERCC4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119113">GDB:119113</A></TD><TD>16p13.13-16p13.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133520">EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 4; ERCC4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278760">XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF</A><BR>
</TD>
</TR>
<TR><TD>FANCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:701221">GDB:701221</A></TD><TD>16q24.3-16q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650">FANCONI ANEMIA, COMPLEMENTATION GROUP A; FACA</A><BR>
</TD>
</TR>
<TR><TD>GALNS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129085">GDB:129085</A></TD><TD>16q24-16q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253000">MUCOPOLYSACCHARIDOSIS TYPE IVA</A><BR>
</TD>
</TR>
<TR><TD>GAN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864885">GDB:9864885</A></TD><TD>16q24.1-16q24.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256850">NEUROPATHY, GIANT AXONAL; GAN</A><BR>
</TD>
</TR>
<TR><TD>HAGH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119292">GDB:119292</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138760">HYDROXYACYL GLUTATHIONE HYDROLASE; HAGH</A><BR>
</TD>
</TR>
<TR><TD>HBA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119293">GDB:119293</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141800">HEMOGLOBIN--ALPHA LOCUS-1; HBA1</A><BR>
</TD>
</TR>
<TR><TD>HBA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119294">GDB:119294</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141850">HEMOGLOBIN--ALPHA LOCUS-2; HBA2</A><BR>
</TD>
</TR>
<TR><TD>HBHR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954541">GDB:9954541</A></TD><TD>16pter-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141750">HEMOGLOBIN H-RELATED MENTAL RETARDATION</A><BR>
</TD>
</TR>
<TR><TD>HBQ1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120036">GDB:120036</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142240">HEMOGLOBIN--THETA-1 LOCUS; HBQ1</A><BR>
</TD>
</TR>
<TR><TD>HBZ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119302">GDB:119302</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142310">HEMOGLOBIN--ZETA LOCUS; HBZ</A><BR>
</TD>
</TR>
<TR><TD>HBZP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120037">GDB:120037</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142310">HEMOGLOBIN--ZETA LOCUS; HBZ</A><BR>
</TD>
</TR>
<TR><TD>HP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119314">GDB:119314</A></TD><TD>16q22.2-16q22.2 16q22.1-16q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=140100">HAPTOGLOBIN; HP</A><BR>
</TD>
</TR>
<TR><TD>HSD11B2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:409951">GDB:409951</A></TD><TD>16q22-16q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=218030">CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>IL4R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118823">GDB:118823</A></TD><TD>16p12.1-16p12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147781">INTERLEUKIN-4 RECEPTOR; IL4R</A><BR>
</TD>
</TR>
<TR><TD>LIPB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119365">GDB:119365</A></TD><TD>16pter-16qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=247980">LIPASE B, LYSOSOMAL ACID; LIPB</A><BR>
</TD>
</TR>
<TR><TD>MC1R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135162">GDB:135162</A></TD><TD>16q24.3-16q24.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=155555">MELANOCORTIN-1 RECEPTOR; MC1R</A><BR>
</TD>
</TR>
<TR><TD>MEFV</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125263">GDB:125263</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=249100">MEDITERRANEAN FEVER, FAMILIAL; MEFV</A><BR>
</TD>
</TR>
<TR><TD>MHC2TA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6268475">GDB:6268475</A></TD><TD>16p13.3-16p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600005">MHC CLASS II TRANSACTIVATOR; MHC2TA</A><BR>
</TD>
</TR>
<TR><TD>MLYCD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11500940">GDB:11500940</A></TD><TD>16q24-16q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248360">MALONYL CoA DECARBOXYLASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>MMVP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11520584">GDB:11520584</A></TD><TD>16p12.1-16p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157700">MITRAL VALVE PROLAPSE, FAMILIAL; MVP</A><BR>
</TD>
</TR>
<TR><TD>PHKB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120286">GDB:120286</A></TD><TD>16q12.1-16q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172490">PHOSPHORYLASE KINASE, BETA SUBUNIT; PHKB</A><BR>
</TD>
</TR>
<TR><TD>PHKG2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:140316">GDB:140316</A></TD><TD>16p11.2-16p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172471">PHOSPHORYLASE KINASE, TESTIS/LIVER, GAMMA 2; PHKG2</A><BR>
</TD>
</TR>
<TR><TD>PKD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120293">GDB:120293</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173900">POLYCYSTIC KIDNEYS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601313">POLYCYSTIC KIDNEY DISEASE 1; PKD1</A><BR>
</TD>
</TR>
<TR><TD>PKDTS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954545">GDB:9954545</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600273">POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS;</A><BR>
</TD>
</TR>
<TR><TD>PMM2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:438697">GDB:438697</A></TD><TD>16p13-16p13 16p13.3-16p13.12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212065">CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I; CDG1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601785">PHOSPHOMANNOMUTASE 2; PMM2</A><BR>
</TD>
</TR>
<TR><TD>PXE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6053895">GDB:6053895</A></TD><TD>16p13.1-16p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177850">PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL DOMINANT; PXE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=264800">PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL RECESSIVE; PXE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603234"></A><BR>
</TD>
</TR>
<TR><TD>SALL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4216161">GDB:4216161</A></TD><TD>16q12.1-16q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107480">TOWNES-BROCKS SYNDROME; TBS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602218">SAL-LIKE 1; SALL1</A><BR>
</TD>
</TR>
<TR><TD>SCA4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250364">GDB:250364</A></TD><TD>16q24-16qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600223">SPINOCEREBELLAR ATAXIA 4; SCA4</A><BR>
</TD>
</TR>
<TR><TD>SCNN1B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:434471">GDB:434471</A></TD><TD>16p12.2-16p12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600760">SODIUM CHANNEL, NONVOLTAGE-GATED 1 BETA; SCNN1B</A><BR>
</TD>
</TR>
<TR><TD>SCNN1G</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:568759">GDB:568759</A></TD><TD>16p12.2-16p12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600761">SODIUM CHANNEL, NONVOLTAGE-GATED 1 GAMMA; SCNN1G</A><BR>
</TD>
</TR>
<TR><TD>SLC12A3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:642135">GDB:642135</A></TD><TD>16q13-16q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600968">SOLUTE CARRIER FAMILY 12, MEMBER 3; SLC12A3</A><BR>
</TD>
</TR>
<TR><TD>TAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120398">GDB:120398</A></TD><TD>16q22.2-16q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=276600">TYROSINE TRANSAMINASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>TSC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120466">GDB:120466</A></TD><TD>16p13.3-16p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191092">TUBEROUS SCLEROSIS-2; TSC2</A><BR>
</TD>
</TR>
<TR><TD>VDI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119629">GDB:119629</A></TD><TD>16pter-16qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125260">DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF</A><BR>
</TD>
</TR>
<TR><TD>WT3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958957">GDB:9958957</A></TD><TD>16q-16q </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=194090">WILMS TUMOR, TYPE III; WT3</A><BR>
</TD>
</TR>
<TR><TD>ABR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119642">GDB:119642</A></TD><TD>17p13.3-17p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600365">ACTIVE BCR-RELATED GENE; ABR</A><BR>
</TD>
</TR>
<TR><TD>ACACA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120534">GDB:120534</A></TD><TD>17q21-17q21 17q12-17q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=200350">ACETYL-CoA CARBOXYLASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>ACADVL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1248185">GDB:1248185</A></TD><TD>17p13-17p13 17p11.2-17p11.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201475">ACYL-CoA DEHYDROGENASE, VERY-LONG-CHAIN, DEFICIENCY OF</A><BR>
</TD>
</TR>
<TR><TD>ACE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119840">GDB:119840</A></TD><TD>17q23-17q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106180">DIPEPTIDYL CARBOXYPEPTIDASE-1; DCP1</A><BR>
</TD>
</TR>
<TR><TD>ALDH3A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1316855">GDB:1316855</A></TD><TD>17p11.2-17p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=270200">SJOGREN-LARSSON SYNDROME; SLS</A><BR>
</TD>
</TR>
<TR><TD>APOH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118887">GDB:118887</A></TD><TD>17q23-17qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138700">APOLIPOPROTEIN H; APOH</A><BR>
</TD>
</TR>
<TR><TD>ASPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:231014">GDB:231014</A></TD><TD>17pter-17p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=271900">SPONGY DEGENERATION OF CENTRAL NERVOUS SYSTEM</A><BR>
</TD>
</TR>
<TR><TD>AXIN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864782">GDB:9864782</A></TD><TD>17q23-17q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114500">CANCER OF COLON</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604025"></A><BR>
</TD>
</TR>
<TR><TD>BCL5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125178">GDB:125178</A></TD><TD>17q22-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151441">LEUKEMIA/LYMPHOMA, CHRONIC B-CELL, 5; BCL5</A><BR>
</TD>
</TR>
<TR><TD>BHD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11498904">GDB:11498904</A></TD><TD>17p11.2-17p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=135150">WITH TRICHODISCOMAS AND ACROCHORDONS</A><BR>
</TD>
</TR>
<TR><TD>BLMH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3801467">GDB:3801467</A></TD><TD>17q11.2-17q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602403">BLEOMYCIN HYDROLASE</A><BR>
</TD>
</TR>
<TR><TD>BRCA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126611">GDB:126611</A></TD><TD>17q21-17q21 17q11-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113705">BREAST CANCER, TYPE 1; BRCA1</A><BR>
</TD>
</TR>
<TR><TD>CACD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5885801">GDB:5885801</A></TD><TD>17p-17p 17p13-17p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215500">CHOROIDAL DYSTROPHY, CENTRAL AREOLAR; CACD</A><BR>
</TD>
</TR>
<TR><TD>CCA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118763">GDB:118763</A></TD><TD>17q24-17q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115660">CATARACT, CONGENITAL, CERULEAN TYPE 1; CCA1</A><BR>
</TD>
</TR>
<TR><TD>CCZS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:681973">GDB:681973</A></TD><TD>17q11-17q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600881">CATARACT, CONGENITAL ZONULAR, WITH SUTURAL OPACITIES; CCZS</A><BR>
</TD>
</TR>
<TR><TD>CHRNB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120587">GDB:120587</A></TD><TD>17p12-17p11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100710">CHOLINERGIC RECEPTOR, NICOTINIC, BETA POLYPEPTIDE 1; CHRNB1</A><BR>
</TD>
</TR>
<TR><TD>CHRNE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132246">GDB:132246</A></TD><TD>17p13-17p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100725">CHOLINERGIC RECEPTOR, NICOTINIC, EPSILON POLYPEPTIDE; CHRNE</A><BR>
</TD>
</TR>
<TR><TD>CMT1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119785">GDB:119785</A></TD><TD>17p12-17p11.2 17p11.2-17p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118220">CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162500">NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP</A><BR>
</TD>
</TR>
<TR><TD>COL1A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119061">GDB:119061</A></TD><TD>17q21.3-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120150">COLLAGEN, TYPE I, ALPHA-1 CHAIN; COL1A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166200">OSTEOGENESIS IMPERFECTA TYPE I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166220">OSTEOGENESIS IMPERFECTA TYPE IV; OI4</A><BR>
</TD>
</TR>
<TR><TD>CORD5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:568473">GDB:568473</A></TD><TD>17p13-17p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600977">CONE-ROD DYSTROPHY-5; CORD5</A><BR>
</TD>
</TR>
<TR><TD>CTNS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:700761">GDB:700761</A></TD><TD>17p-17p 17p13-17p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=219800">CYSTINOSIS, EARLY-ONSET OR INFANTILE NEPHROPATHIC TYPE</A><BR>
</TD>
</TR>
<TR><TD>EPX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:377700">GDB:377700</A></TD><TD>17q23.1-17q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131399">EOSINOPHIL PEROXIDASE; EPX</A><BR>
</TD>
</TR>
<TR><TD>ERBB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120613">GDB:120613</A></TD><TD>17q11.2-17q12 17q21.1-17q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164870">V-ERB-B2 AVIAN ERYTHROBLASTIC LEUKEMIA VIRAL ONCOGENE HOMOLOG 2; ERBB2</A><BR>
</TD>
</TR>
<TR><TD>G6PC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:231927">GDB:231927</A></TD><TD>17q21-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232200">GLYCOGEN STORAGE DISEASE I; GSD-I</A><BR>
</TD>
</TR>
<TR><TD>GAA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119965">GDB:119965</A></TD><TD>17q23-17q23 17q25.2-17q25.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232300">GLYCOGEN STORAGE DISEASE II</A><BR>
</TD>
</TR>
<TR><TD>GALK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119246">GDB:119246</A></TD><TD>17q24-17q24 17q23-17q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=230200">GALACTOKINASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>GCGR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:304516">GDB:304516</A></TD><TD>17q25-17q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138033">GLUCAGON RECEPTOR; GCGR</A><BR>
</TD>
</TR>
<TR><TD>GFAP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118799">GDB:118799</A></TD><TD>17q21-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137780">GLIAL FIBRILLARY ACIDIC PROTEIN; GFAP</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=203450">ALEXANDER DISEASE</A><BR>
</TD>
</TR>
<TR><TD>GH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119982">GDB:119982</A></TD><TD>17q22-17q24 17q23.1-17q23.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139250">GROWTH HORMONE 1; GH1</A><BR>
</TD>
</TR>
<TR><TD>GH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119983">GDB:119983</A></TD><TD>17q22-17q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139240">GROWTH HORMONE 2; GH2</A><BR>
</TD>
</TR>
<TR><TD>GP1BA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118806">GDB:118806</A></TD><TD>17pter-17p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231200">GIANT PLATELET SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>GPSC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954564">GDB:9954564</A></TD><TD>17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=221820">FAMILIAL PROGRESSIVE SUBCORTICAL</A><BR>
</TD>
</TR>
<TR><TD>GUCY2D</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136012">GDB:136012</A></TD><TD>17p13-17p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204000">AMAUROSIS CONGENITA OF LEBER I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600179">GUANYLATE CYCLASE 2D, MEMBRANE; GUC2D</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601777">CONE-ROD DYSTROPHY-6; CORD6</A><BR>
</TD>
</TR>
<TR><TD>ITGA2B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120012">GDB:120012</A></TD><TD>17q21.32-17q21.32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=273800">THROMBASTHENIA OF GLANZMANN AND NAEGELI</A><BR>
</TD>
</TR>
<TR><TD>ITGB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120013">GDB:120013</A></TD><TD>17q21.32-17q21.32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173470">INTEGRIN, BETA-3; ITGB3</A><BR>
</TD>
</TR>
<TR><TD>ITGB4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128028">GDB:128028</A></TD><TD>17q11-17qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147557">INTEGRIN, BETA-4; ITGB4</A><BR>
</TD>
</TR>
<TR><TD>KRT10</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118828">GDB:118828</A></TD><TD>17q12-17q21 17q21-17q22 17q21.1-17q21.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148080">KERATIN 10; KRT10</A><BR>
</TD>
</TR>
<TR><TD>KRT12</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5583953">GDB:5583953</A></TD><TD>17q11-17q12 17q12-17q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122100">CORNEAL DYSTROPHY, JUVENILE EPITHELIAL, OF MEESMANN</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601687">KERATIN 12; KRT12</A><BR>
</TD>
</TR>
<TR><TD>KRT13</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120740">GDB:120740</A></TD><TD>17q21-17q23 17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148065">KERATIN 13; KRT13</A><BR>
</TD>
</TR>
<TR><TD>KRT14</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132145">GDB:132145</A></TD><TD>17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148066">KERATIN 14; KRT14</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601001">GLUTATHIONE SYNTHETASE; GSS</A><BR>
</TD>
</TR>
<TR><TD>KRT14L1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120121">GDB:120121</A></TD><TD>17p12-17p11 17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148066">KERATIN 14; KRT14</A><BR>
</TD>
</TR>
<TR><TD>KRT14L2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120122">GDB:120122</A></TD><TD>17p12-17p11 17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148066">KERATIN 14; KRT14</A><BR>
</TD>
</TR>
<TR><TD>KRT14L3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120123">GDB:120123</A></TD><TD>17p12-17p11 17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148066">KERATIN 14; KRT14</A><BR>
</TD>
</TR>
<TR><TD>KRT16</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136207">GDB:136207</A></TD><TD>17pter-17qter 17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148067">KERATIN 16; KRT16</A><BR>
</TD>
</TR>
<TR><TD>KRT16L1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120125">GDB:120125</A></TD><TD>17p12-17p11 17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148067">KERATIN 16; KRT16</A><BR>
</TD>
</TR>
<TR><TD>KRT16L2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120126">GDB:120126</A></TD><TD>17p12-17p11 17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148067">KERATIN 16; KRT16</A><BR>
</TD>
</TR>
<TR><TD>KRT17</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136211">GDB:136211</A></TD><TD>17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148069">KERATIN 17; KRT17</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=167210">PACHYONYCHIA CONGENITA, JACKSON-LAWLER TYPE</A><BR>
</TD>
</TR>
<TR><TD>KRT9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:303970">GDB:303970</A></TD><TD>17q12-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=144200">HYPERKERATOSIS, LOCALIZED EPIDERMOLYTIC</A><BR>
</TD>
</TR>
<TR><TD>MAPT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119434">GDB:119434</A></TD><TD>17q21-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=157140">MICROTUBULE-ASSOCIATED PROTEIN TAU; MAPT</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168610">PALLIDOPONTONIGRAL DEGENERATION; PPND</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600274">DISINHIBITION-DEMENTIA-PARKINSONISM-AMYOTROPHY COMPLEX; DDPAC</A><BR>
</TD>
</TR>
<TR><TD>MDB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958959">GDB:9958959</A></TD><TD>17p13.1-17p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=155255">MEDULLOBLASTOMA; MDB</A><BR>
</TD>
</TR>
<TR><TD>MDCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120525">GDB:120525</A></TD><TD>17p13.3-17p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=247200">MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601545">PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, GAMMA SUBUNIT</A><BR>
</TD>
</TR>
<TR><TD>MGI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954550">GDB:9954550</A></TD><TD>17p13-17p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254210">MYASTHENIA GRAVIS, FAMILIAL INFANTILE; FIMG</A><BR>
</TD>
</TR>
<TR><TD>MHS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132580">GDB:132580</A></TD><TD>17q11.2-17q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154275">MALIGNANT HYPERTHERMIA SUSCEPTIBILITY-2; MHS2</A><BR>
</TD>
</TR>
<TR><TD>MKS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:681967">GDB:681967</A></TD><TD>17q21-17q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=249000">MECKEL SYNDROME; MKS</A><BR>
</TD>
</TR>
<TR><TD>MPO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120192">GDB:120192</A></TD><TD>17q21.3-17q23 17q23.1-17q23.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254600">MYELOPEROXIDASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>MYO15A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9838006">GDB:9838006</A></TD><TD>17p11.2-17p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600316">DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 3; DFNB3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602666"></A><BR>
</TD>
</TR>
<TR><TD>NAGLU</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:636533">GDB:636533</A></TD><TD>17q21.1-17q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252920">MUCOPOLYSACCHARIDOSIS TYPE IIIB</A><BR>
</TD>
</TR>
<TR><TD>NAPB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954572">GDB:9954572</A></TD><TD>17q25-17q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162100">NEURITIS WITH BRACHIAL PREDILECTION; NAPB</A><BR>
</TD>
</TR>
<TR><TD>NF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120231">GDB:120231</A></TD><TD>17q11.2-17q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162200">NEUROFIBROMATOSIS, TYPE I; NF1</A><BR>
</TD>
</TR>
<TR><TD>NME1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127965">GDB:127965</A></TD><TD>17q21-17q22 17q21.3-17q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156490">NON-METASTATIC CELLS 1, PROTEIN EXPRESSED IN; NME1</A><BR>
</TD>
</TR>
<TR><TD>P4HB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120708">GDB:120708</A></TD><TD>17q25-17q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176790">PROLYL-4-HYDROXYLASE, BETA POLYPEPTIDE; PHDB; PROHB</A><BR>
</TD>
</TR>
<TR><TD>PAFAH1B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:677430">GDB:677430</A></TD><TD>17p13.3-17p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=247200">MILLER-DIEKER LISSENCEPHALY SYNDROME; MDLS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601545">PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, GAMMA SUBUNIT</A><BR>
</TD>
</TR>
<TR><TD>PECAM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:696372">GDB:696372</A></TD><TD>17q23-17q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173445">PLATELET-ENDOTHELIAL CELL ADHESION MOLECULE; PECAM1</A><BR>
</TD>
</TR>
<TR><TD>PEX12</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6155804">GDB:6155804</A></TD><TD>17q21.1-17q21.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=214100">ZELLWEGER SYNDROME; ZS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601758">PEROXIN-12; PEX12</A><BR>
</TD>
</TR>
<TR><TD>PHB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126600">GDB:126600</A></TD><TD>17q21-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176705">PROHIBITIN; PHB</A><BR>
</TD>
</TR>
<TR><TD>PMP22</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134190">GDB:134190</A></TD><TD>17p11.2-17p11.2 17p12-17p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118220">CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A; CMT1A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145900">HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601097">PERIPHERAL MYELIN PROTEIN 22; PMP22</A><BR>
</TD>
</TR>
<TR><TD>PRKAR1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120313">GDB:120313</A></TD><TD>17q23-17q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160980">MYXOMA, SPOTTY PIGMENTATION, AND ENDOCRINE OVERACTIVITY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188830">PROTEIN KINASE, cAMP-DEPENDENT, REGULATORY, TYPE I, ALPHA; PRKAR1A</A><BR>
</TD>
</TR>
<TR><TD>PRKCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128015">GDB:128015</A></TD><TD>17q22-17q24 17q22-17q23.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176960">PROTEIN KINASE C, ALPHA; PRKCA</A><BR>
</TD>
</TR>
<TR><TD>PRKWNK4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954566">GDB:9954566</A></TD><TD>17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601844">PSEUDOHYPOALDOSTERONISM TYPE II, LOCUS B; PHA2B</A><BR>
</TD>
</TR>
<TR><TD>PRP8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957697">GDB:9957697</A></TD><TD>17p13.3-17p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600059">RETINITIS PIGMENTOSA-13; RP13</A><BR>
</TD>
</TR>
<TR><TD>PRPF8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:392647">GDB:392647</A></TD><TD>17p-17p 17p13.3-17p13.2 17p13.3-17p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600059">RETINITIS PIGMENTOSA-13; RP13</A><BR>
</TD>
</TR>
<TR><TD>PTLAH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957342">GDB:9957342</A></TD><TD>17q-17q 17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=168860">APLASIA OR HYPOPLASIA</A><BR>
</TD>
</TR>
<TR><TD>RARA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120337">GDB:120337</A></TD><TD>17q12-17q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180240">RETINOIC ACID RECEPTOR, ALPHA; RARA</A><BR>
</TD>
</TR>
<TR><TD>RCV1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135477">GDB:135477</A></TD><TD>17p13-17p12 17p13.1-17p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179618">RECOVERIN; RCV1</A><BR>
</TD>
</TR>
<TR><TD>RMSA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:304519">GDB:304519</A></TD><TD>17p12-17p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=179715">REGULATOR OF MITOTIC SPINDLE ASSEMBLY 1; RMSA1</A><BR>
</TD>
</TR>
<TR><TD>RP17</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:683199">GDB:683199</A></TD><TD>17q22-17q24 17q22-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600852">RETINITIS PIGMENTOSA-17; RP17</A><BR>
</TD>
</TR>
<TR><TD>RSS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439249">GDB:439249</A></TD><TD>17q25-17q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180860">RUSSELL-SILVER SYNDROME; RSS</A><BR>
</TD>
</TR>
<TR><TD>SCN4A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125181">GDB:125181</A></TD><TD>17q22-17q24 17q23.1-17q25.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170500">PERIODIC PARALYSIS II</A><BR>
</TD>
</TR>
<TR><TD>SERPINF2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120301">GDB:120301</A></TD><TD>17p13-17p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=262850">PLASMIN INHIBITOR DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>SGCA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:384077">GDB:384077</A></TD><TD>17q21-17q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600119">ADHALIN; ADL</A><BR>
</TD>
</TR>
<TR><TD>SGSH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1319101">GDB:1319101</A></TD><TD>17q25.3-17q25.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252900">MUCOPOLYSACCHARIDOSIS TYPE IIIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605270"></A><BR>
</TD>
</TR>
<TR><TD>SHBG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125280">GDB:125280</A></TD><TD>17pter-17p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182205">SEX HORMONE BINDING GLOBULIN; SHBG</A><BR>
</TD>
</TR>
<TR><TD>SLC2A4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119997">GDB:119997</A></TD><TD>17p13-17p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138190">SOLUTE CARRIER FAMILY 2, MEMBER 4; SLC2A4</A><BR>
</TD>
</TR>
<TR><TD>SLC4A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119874">GDB:119874</A></TD><TD>17q12-17q21 17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109270">SOLUTE CARRIER FAMILY 4, ANION EXCHANGER, MEMBER 1; SLC4A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=110500">BLOOD GROUP--DIEGO SYSTEM; DI</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=112050">BLOOD GROUP--WRIGHT ANTIGEN; Wr</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130600">ELLIPTOCYTOSIS, RHESUS-UNLINKED TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=166900">HEREDITARY HEMOLYTIC</A><BR>
</TD>
</TR>
<TR><TD>SLC6A4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134713">GDB:134713</A></TD><TD>17q11.1-17q12 17q12-17q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182138">SOLUTE CARRIER FAMILY 6, MEMBER 4; SLC6A4</A><BR>
</TD>
</TR>
<TR><TD>SMCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120379">GDB:120379</A></TD><TD>17p11.2-17p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182290">SMITH-MAGENIS SYNDROME; SMS</A><BR>
</TD>
</TR>
<TR><TD>SOST</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10450629">GDB:10450629</A></TD><TD>17q12-17q21 17q21.31-17q21.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=269500">SCLEROSTEOSIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605740"></A><BR>
</TD>
</TR>
<TR><TD>SOX9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134730">GDB:134730</A></TD><TD>17q24.3-17q25.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114290">DYSPLASIA</A><BR>
</TD>
</TR>
<TR><TD>SSTR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134186">GDB:134186</A></TD><TD>17q24-17q24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182452">SOMATOSTATIN RECEPTOR-2; SSTR2</A><BR>
</TD>
</TR>
<TR><TD>SYM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:512174">GDB:512174</A></TD><TD>17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=185800">SYMPHALANGISM, PROXIMAL; SYM1</A><BR>
</TD>
</TR>
<TR><TD>SYNS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9862343">GDB:9862343</A></TD><TD>17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=186500">SYNOSTOSES, MULTIPLE, WITH BRACHYDACTYLY</A><BR>
</TD>
</TR>
<TR><TD>TCF2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125298">GDB:125298</A></TD><TD>17q11.2-17q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=189907">TRANSCRIPTION FACTOR-2, HEPATIC; TCF2</A><BR>
</TD>
</TR>
<TR><TD>THRA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120730">GDB:120730</A></TD><TD>17q11.2-17q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190120">THYROID HORMONE RECEPTOR, ALPHA 1; THRA</A><BR>
</TD>
</TR>
<TR><TD>TIMP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132612">GDB:132612</A></TD><TD>17q25-17q25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188825">TISSUE INHIBITOR OF METALLOPROTEINASE-2; TIMP2</A><BR>
</TD>
</TR>
<TR><TD>TOC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:451978">GDB:451978</A></TD><TD>17q24-17q24 17q23-17qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148500">TYLOSIS WITH ESOPHAGEAL CANCER; TOC</A><BR>
</TD>
</TR>
<TR><TD>TOP2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118884">GDB:118884</A></TD><TD>17q21-17q22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126430">TOPOISOMERASE (DNA) II, ALPHA; TOP2A</A><BR>
</TD>
</TR>
<TR><TD>TP53</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120445">GDB:120445</A></TD><TD>17p13.1-17p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114550">CANCER, HEPATOCELLULAR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151623">LI-FRAUMENI SYNDROME; LFS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191170">TUMOR PROTEIN p53; TP53</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=260350">CARCINOMA</A><BR>
</TD>
</TR>
<TR><TD>TRIM37</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:636050">GDB:636050</A></TD><TD>17q-17q 17q21.3-17q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253250">MULIBREY NANISM; MUL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605073"></A><BR>
</TD>
</TR>
<TR><TD>VBCH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954554">GDB:9954554</A></TD><TD>17q11.2-17q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=239100">HYPEROSTOSIS CORTICALIS GENERALISATA</A><BR>
</TD>
</TR>
<TR><TD>ATP8B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:453352">GDB:453352</A></TD><TD>18q-18q 18q21-18q22 18q21-18q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=211600">CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1; PFIC1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=243300">INTRAHEPATIC CHOLESTASIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602397">FAMILIAL INTRAHEPATIC CHOLESTASIS-1; FIC1</A><BR>
</TD>
</TR>
<TR><TD>BCL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119031">GDB:119031</A></TD><TD>18q21.33-18q21.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151430">B-CELL CLL/LYMPHOMA 2; BCL2</A><BR>
</TD>
</TR>
<TR><TD>CNSN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954580">GDB:9954580</A></TD><TD>18q21.3-18q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212200">CARNOSINEMIA</A><BR>
</TD>
</TR>
<TR><TD>CORD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118773">GDB:118773</A></TD><TD>18q21.1-18q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600624">CONE-ROD DYSTROPHY-1; CORD1</A><BR>
</TD>
</TR>
<TR><TD>CYB5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125236">GDB:125236</A></TD><TD>18q22.3-18q23 18q23-18q23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250790">METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5</A><BR>
</TD>
</TR>
<TR><TD>DCC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119838">GDB:119838</A></TD><TD>18q21.1-18q21.1 18q21.3-18q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120470">DELETED IN COLORECTAL CARCINOMA; DCC</A><BR>
</TD>
</TR>
<TR><TD>F5F8D</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6919858">GDB:6919858</A></TD><TD>18q21-18q21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227300">FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF; F5F8D</A><BR>
</TD>
</TR>
<TR><TD>FECH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127282">GDB:127282</A></TD><TD>18q21.1-18q21.31 18q21.3-18q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177000">PROTOPORPHYRIA, ERYTHROPOIETIC</A><BR>
</TD>
</TR>
<TR><TD>FEO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4378120">GDB:4378120</A></TD><TD>18q21.3-18q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=174810">POLYOSTOTIC OSTEOLYTIC DYSPLASIA, HEREDITARY EXPANSILE; HEPOD</A><BR>
</TD>
</TR>
<TR><TD>LAMA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:251818">GDB:251818</A></TD><TD>18q11.2-18q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600805">LAMININ, ALPHA 3; LAMA3</A><BR>
</TD>
</TR>
<TR><TD>LCFS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954578">GDB:9954578</A></TD><TD>18q11-18q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114400">CANCER</A><BR>
</TD>
</TR>
<TR><TD>MADH4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4642788">GDB:4642788</A></TD><TD>18q21.1-18q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=174900">POLYPOSIS, JUVENILE INTESTINAL</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600993">MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 4; MADH4</A><BR>
</TD>
</TR>
<TR><TD>MAFD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120163">GDB:120163</A></TD><TD>18p-18p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125480">MANIC-DEPRESSIVE PSYCHOSIS, AUTOSOMAL</A><BR>
</TD>
</TR>
<TR><TD>MC2R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135163">GDB:135163</A></TD><TD>18p11.2-18p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=202200">ADRENAL UNRESPONSIVENESS TO ACTH</A><BR>
</TD>
</TR>
<TR><TD>MCL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954574">GDB:9954574</A></TD><TD>18p11.32-18p11.32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=150800">LEIOMYOMATA, HEREDITARY MULTIPLE, OF SKIN</A><BR>
</TD>
</TR>
<TR><TD>MYP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9862232">GDB:9862232</A></TD><TD>18p11.31-18p11.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160700">MYOPIA</A><BR>
</TD>
</TR>
<TR><TD>NPC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138178">GDB:138178</A></TD><TD>18q11-18q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=257220">NIEMANN-PICK DISEASE, TYPE C1; NPC1</A><BR>
</TD>
</TR>
<TR><TD>SPPK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:606444">GDB:606444</A></TD><TD>18q12-18q12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148700">PALMOPLANTARIS STRIATA</A><BR>
</TD>
</TR>
<TR><TD>TGFBRE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250852">GDB:250852</A></TD><TD>18q22-18qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=275355">TRANSFORMING GROWTH FACTOR, BETA 1 RESPONSE ELEMENT</A><BR>
</TD>
</TR>
<TR><TD>TGIF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9787150">GDB:9787150</A></TD><TD>18p11.3-18p11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142946">HOLOPROSENCEPHALY, TYPE 4; HPE4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602630"></A><BR>
</TD>
</TR>
<TR><TD>TTR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119471">GDB:119471</A></TD><TD>18q12.1-18q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176300">TRANSTHYRETIN; TTR</A><BR>
</TD>
</TR>
<TR><TD>AD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118748">GDB:118748</A></TD><TD>19pter-19qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104310">ALZHEIMER DISEASE-2; AD2</A><BR>
</TD>
</TR>
<TR><TD>AMH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118996">GDB:118996</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261550">PERSISTENT MULLERIAN DUCT SYNDROME, TYPES I AND II; PMDS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600957">ANTI-MULLERIAN HORMONE; AMH</A><BR>
</TD>
</TR>
<TR><TD>APOC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119689">GDB:119689</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=207750">APOLIPOPROTEIN C-II DEFICIENCY, TYPE I HYPERLIPOPROTEINEMIA DUE TO</A><BR>
</TD>
</TR>
<TR><TD>APOE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119691">GDB:119691</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=107741">APOLIPOPROTEIN E; APOE</A><BR>
</TD>
</TR>
<TR><TD>ATHS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128803">GDB:128803</A></TD><TD>19p13.3-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108725">LIPOPROTEIN PHENOTYPE; ALP</A><BR>
</TD>
</TR>
<TR><TD>BAX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:228082">GDB:228082</A></TD><TD>19q13.3-19q13.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600040">BCL2-ASSOCIATED X PROTEIN; BAX</A><BR>
</TD>
</TR>
<TR><TD>BCKDHA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119723">GDB:119723</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248600">MAPLE SYRUP URINE DISEASE</A><BR>
</TD>
</TR>
<TR><TD>BCL3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120561">GDB:120561</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=109560">B-CELL LEUKEMIA/LYMPHOMA-3; BCL3</A><BR>
</TD>
</TR>
<TR><TD>BFIC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954584">GDB:9954584</A></TD><TD>19q12-19q13.11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601764">BENIGN FAMILIAL INFANTILE CONVULSIONS</A><BR>
</TD>
</TR>
<TR><TD>C3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119044">GDB:119044</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120700">COMPLEMENT COMPONENT-3; C3</A><BR>
</TD>
</TR>
<TR><TD>CACNA1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126432">GDB:126432</A></TD><TD>19p13-19p13 19p13.1-19p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108500">ATAXIA, PERIODIC VESTIBULOCEREBELLAR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=141500">HEMIPLEGIC MIGRAINE, FAMILIAL; MHP</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=183086">SPINOCEREBELLAR ATAXIA 6; SCA6</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601011">CALCIUM CHANNEL, VOLTAGE-DEPENDENT, P/Q TYPE, ALPHA 1A SUBUNIT; CACNA1A</A><BR>
</TD>
</TR>
<TR><TD>CCO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119755">GDB:119755</A></TD><TD>19q12-19q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=117000">CENTRAL CORE DISEASE OF MUSCLE</A><BR>
</TD>
</TR>
<TR><TD>CEACAM5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119054">GDB:119054</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114890">CARCINOEMBRYONIC ANTIGEN; CEA</A><BR>
</TD>
</TR>
<TR><TD>COMP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:344263">GDB:344263</A></TD><TD>19p13.1-19p13.1 19pter-19qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=132400">EPIPHYSEAL DYSPLASIA, MULTIPLE; MED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177170">PSEUDOACHONDROPLASTIC DYSPLASIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600310">CARTILAGE OLIGOMERIC MATRIX PROTEIN; COMP</A><BR>
</TD>
</TR>
<TR><TD>CRX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:333932">GDB:333932</A></TD><TD>19q13.3-19q13.4 19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120970">CONE-ROD DYSTROPHY-2; CORD2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204000">AMAUROSIS CONGENITA OF LEBER I</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602225">CONE-ROD HOMEO BOX-CONTAINING GENE</A><BR>
</TD>
</TR>
<TR><TD>DBA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9600353">GDB:9600353</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=205900">ANEMIA, CONGENITAL HYPOPLASTIC, OF BLACKFAN AND DIAMOND</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=603474"></A><BR>
</TD>
</TR>
<TR><TD>DDU</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10796026">GDB:10796026</A></TD><TD>19p-19p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125630">URTICARIA; DDU</A><BR>
</TD>
</TR>
<TR><TD>DFNA4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:606540">GDB:606540</A></TD><TD>19q13-19q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600652">DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 4; DFNA4</A><BR>
</TD>
</TR>
<TR><TD>DLL3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9959026">GDB:9959026</A></TD><TD>19q13.1-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277300">VERTEBRAL ANOMALIES</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602768"></A><BR>
</TD>
</TR>
<TR><TD>DM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119097">GDB:119097</A></TD><TD>19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160900">DYSTROPHIA MYOTONICA; DM</A><BR>
</TD>
</TR>
<TR><TD>DMWD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:7178354">GDB:7178354</A></TD><TD>19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=160900">DYSTROPHIA MYOTONICA; DM</A><BR>
</TD>
</TR>
<TR><TD>E11S</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119101">GDB:119101</A></TD><TD>19q13.1-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=129150">ECHO 11 SENSITIVITY; E11S</A><BR>
</TD>
</TR>
<TR><TD>ELA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118792">GDB:118792</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130130">ELASTASE-2; ELA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=162800">NEUTROPENIA, CYCLIC</A><BR>
</TD>
</TR>
<TR><TD>EPOR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125242">GDB:125242</A></TD><TD>19p13.2-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133171">ERYTHROPOIETIN RECEPTOR; EPOR</A><BR>
</TD>
</TR>
<TR><TD>ERCC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119112">GDB:119112</A></TD><TD>19q13.2-19q13.2 19q13.2-19q13.3 19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126340">EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 2; ERCC2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=278730">XERODERMA PIGMENTOSUM IV; XP4</A><BR>
</TD>
</TR>
<TR><TD>ETFB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119887">GDB:119887</A></TD><TD>19q13.3-19q13.3 19q13.4-19q13.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130410">ELECTRON TRANSFER FLAVOPROTEIN, BETA POLYPEPTIDE; ETFB</A><BR>
</TD>
</TR>
<TR><TD>EXT3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:383780">GDB:383780</A></TD><TD>19p-19p 19p13-19p13 19p13.2-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600209">EXOSTOSES, MULTIPLE, TYPE III; EXT3</A><BR>
</TD>
</TR>
<TR><TD>EYCL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119269">GDB:119269</A></TD><TD>19q12-19q13 19pter-19qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227240">EYE COLOR-1; EYCL1</A><BR>
</TD>
</TR>
<TR><TD>FTL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119234">GDB:119234</A></TD><TD>19q13.3-19q13.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134790">FERRITIN LIGHT CHAIN; FTL</A><BR>
</TD>
</TR>
<TR><TD>FUT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120618">GDB:120618</A></TD><TD>19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=211100">FUCOSYLTRANSFERASE-1; FUT1</A><BR>
</TD>
</TR>
<TR><TD>FUT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120619">GDB:120619</A></TD><TD>19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182100">FUCOSYLTRANSFERASE-2; FUT2</A><BR>
</TD>
</TR>
<TR><TD>FUT6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135180">GDB:135180</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136836">FUCOSYLTRANSFERASE-6; FUT6</A><BR>
</TD>
</TR>
<TR><TD>GAMT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1313736">GDB:1313736</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601240">GUANIDINOACETATE METHYLTRANSFERASE; GAMT</A><BR>
</TD>
</TR>
<TR><TD>GCDH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136004">GDB:136004</A></TD><TD>19p13.2-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231670">GLUTARICACIDEMIA I</A><BR>
</TD>
</TR>
<TR><TD>GPI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120015">GDB:120015</A></TD><TD>19q13.1-19q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=172400">GLUCOSEPHOSPHATE ISOMERASE; GPI</A><BR>
</TD>
</TR>
<TR><TD>GUSM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119291">GDB:119291</A></TD><TD>19pter-19qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231610">GLUCURONIDASE, MOUSE, MODIFIER OF; GUSM</A><BR>
</TD>
</TR>
<TR><TD>HB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954586">GDB:9954586</A></TD><TD>19q13.2-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113900">BUNDLE BRANCH BLOCK</A><BR>
</TD>
</TR>
<TR><TD>HCL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119304">GDB:119304</A></TD><TD>19q12-19q13 19pter-19qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=113750">HAIR COLOR-1; HCL1</A><BR>
</TD>
</TR>
<TR><TD>HHC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:249836">GDB:249836</A></TD><TD>19p-19p </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145981">HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II; HHC2</A><BR>
</TD>
</TR>
<TR><TD>HHC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955121">GDB:9955121</A></TD><TD>19q13-19q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600740">HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III; HHC3</A><BR>
</TD>
</TR>
<TR><TD>ICAM3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136236">GDB:136236</A></TD><TD>19p13.3-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146631">INTERCELLULAR ADHESION MOLECULE-3; ICAM3</A><BR>
</TD>
</TR>
<TR><TD>INSR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119352">GDB:119352</A></TD><TD>19p13.2-19p13.2 19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147670">INSULIN RECEPTOR; INSR</A><BR>
</TD>
</TR>
<TR><TD>JAK3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:376460">GDB:376460</A></TD><TD>19p13.1-19p12 19p13.1-19p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600173">JANUS KINASE 3 JAK3</A><BR>
</TD>
</TR>
<TR><TD>KLK3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119695">GDB:119695</A></TD><TD>19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176820">ANTIGEN, PROSTATE-SPECIFIC; APS</A><BR>
</TD>
</TR>
<TR><TD>LDLR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119362">GDB:119362</A></TD><TD>19p13.2-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=143890">HYPERCHOLESTEROLEMIA, FAMILIAL; FHC</A><BR>
</TD>
</TR>
<TR><TD>LHB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119364">GDB:119364</A></TD><TD>19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=152780">LUTEINIZING HORMONE, BETA POLYPEPTIDE; LHB</A><BR>
</TD>
</TR>
<TR><TD>LIG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127274">GDB:127274</A></TD><TD>19q13.3-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126391">LIGASE I, DNA, ATP-DEPENDENT; LIG1</A><BR>
</TD>
</TR>
<TR><TD>LOH19CR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9837482">GDB:9837482</A></TD><TD>19q13-19q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=205900">ANEMIA, CONGENITAL HYPOPLASTIC, OF BLACKFAN AND DIAMOND</A><BR>
</TD>
</TR>
<TR><TD>LYL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120158">GDB:120158</A></TD><TD>19p13.2-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151440">LEUKEMIA, LYMPHOID, 1; LYL1</A><BR>
</TD>
</TR>
<TR><TD>MAN2B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119376">GDB:119376</A></TD><TD>19cen-19cen </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248500">MANNOSIDOSIS, ALPHA B, LYSOSOMAL</A><BR>
</TD>
</TR>
<TR><TD>MCOLN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10013974">GDB:10013974</A></TD><TD>19p13.3-19p13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=252650">MUCOLIPIDOSIS IV</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605248"></A><BR>
</TD>
</TR>
<TR><TD>MDRV</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6306714">GDB:6306714</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601846">MUSCULAR DYSTROPHY, AUTOSOMAL DOMINANT, WITH RIMMED VACUOLES; MDRV</A><BR>
</TD>
</TR>
<TR><TD>MLLT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136791">GDB:136791</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159556">MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 1; MLLT1</A><BR>
</TD>
</TR>
<TR><TD>NOTCH3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:361163">GDB:361163</A></TD><TD>19p-19p 19q12-19q12 19p13.2-19p13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125310">DEMENTIA, HEREDITARY MULTI-INFARCT TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600276">NOTCH, DROSOPHILA, HOMOLOG OF, 3; NOTCH3</A><BR>
</TD>
</TR>
<TR><TD>NPHS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:342105">GDB:342105</A></TD><TD>19q12-19q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256300">NEPHROSIS 1, CONGENITAL, FINNISH TYPE; NPHS1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602716"></A><BR>
</TD>
</TR>
<TR><TD>OFC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128060">GDB:128060</A></TD><TD>19q13-19q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600757">OROFACIAL CLEFT-3; OFC3</A><BR>
</TD>
</TR>
<TR><TD>OPA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954590">GDB:9954590</A></TD><TD>19q13.2-19q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=258501">OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA</A><BR>
</TD>
</TR>
<TR><TD>PEPD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120273">GDB:120273</A></TD><TD>19cen-19q13.11 19q13.1-19q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170100">PEPTIDASE D; PEPD</A><BR>
</TD>
</TR>
<TR><TD>PRPF31</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:333911">GDB:333911</A></TD><TD>19q13.4-19q13.4 19q13.42-19q13.42 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600138">RETINITIS PIGMENTOSA 11; RP11</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=606419"></A><BR>
</TD>
</TR>
<TR><TD>PRTN3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126876">GDB:126876</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=177020">PROTEINASE 3; PRTN3; PR3</A><BR>
</TD>
</TR>
<TR><TD>PRX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11501256">GDB:11501256</A></TD><TD>19q13.13-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145900">HYPERTROPHIC NEUROPATHY OF DEJERINE-SOTTAS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=605725"></A><BR>
</TD>
</TR>
<TR><TD>PSG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120321">GDB:120321</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176390">PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN 1; PSG1</A><BR>
</TD>
</TR>
<TR><TD>PVR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120324">GDB:120324</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=173850">POLIOVIRUS SUSCEPTIBILITY, OR SENSITIVITY; PVS</A><BR>
</TD>
</TR>
<TR><TD>RYR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120359">GDB:120359</A></TD><TD>19q12-19q13.2 19q13.1-19q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=117000">CENTRAL CORE DISEASE OF MUSCLE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145600">HYPERTHERMIA OF ANESTHESIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180901">RYANODINE RECEPTOR-1; RYR1</A><BR>
</TD>
</TR>
<TR><TD>SLC5A5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5892184">GDB:5892184</A></TD><TD>19p13.2-19p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601843">SOLUTE CARRIER FAMILY 5, MEMBER 5; SLC5A5</A><BR>
</TD>
</TR>
<TR><TD>SLC7A9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958852">GDB:9958852</A></TD><TD>19q13.1-19q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600918">CYSTINURIA, TYPE III; CSNU3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604144"></A><BR>
</TD>
</TR>
<TR><TD>STK11</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9732383">GDB:9732383</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=175200">PEUTZ-JEGHERS SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602216">SERINE/THREONINE PROTEIN KINASE 11; STK11</A><BR>
</TD>
</TR>
<TR><TD>TBXA2R</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127517">GDB:127517</A></TD><TD>19p13.3-19p13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188070">THROMBOXANE A2 RECEPTOR, PLATELET; TBXA2R</A><BR>
</TD>
</TR>
<TR><TD>TGFB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120729">GDB:120729</A></TD><TD>19q13.2-19q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131300">ENGELMANN DISEASE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190180">TRANSFORMING GROWTH FACTOR, BETA-1; TGFB1</A><BR>
</TD>
</TR>
<TR><TD>TNNI3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125309">GDB:125309</A></TD><TD>19p13.2-19q13.2 19q13.4-19q13.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=191044">TROPONIN I, CARDIAC; TNNI3</A><BR>
</TD>
</TR>
<TR><TD>TYROBP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954457">GDB:9954457</A></TD><TD>19q13.1-19q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=221770">POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604142"></A><BR>
</TD>
</TR>
<TR><TD>ADA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119649">GDB:119649</A></TD><TD>20q12-20q13.11 20q13.11-20q13.11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=102700">ADENOSINE DEAMINASE; ADA</A><BR>
</TD>
</TR>
<TR><TD>AHCY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118983">GDB:118983</A></TD><TD>20cen-20q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180960">S-ADENOSYLHOMOCYSTEINE HYDROLASE; AHCY</A><BR>
</TD>
</TR>
<TR><TD>AVP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119009">GDB:119009</A></TD><TD>20p13-20p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125700">DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=192340">ARGININE VASOPRESSIN; AVP</A><BR>
</TD>
</TR>
<TR><TD>CDAN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9823270">GDB:9823270</A></TD><TD>20q11.2-20q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=224100">DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE II</A><BR>
</TD>
</TR>
<TR><TD>CDPD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11505748">GDB:11505748</A></TD><TD>20p13-20p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217400">DYSTROPHY AND PERCEPTIVE DEAFNESS</A><BR>
</TD>
</TR>
<TR><TD>CHED1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3837719">GDB:3837719</A></TD><TD>20p11.2-20q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121700">CORNEAL DYSTROPHY, CONGENITAL ENDOTHELIAL; CHED</A><BR>
</TD>
</TR>
<TR><TD>CHED2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957389">GDB:9957389</A></TD><TD>20p13-20p13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217700">CORNEAL DYSTROPHY, CONGENITAL HEREDITARY</A><BR>
</TD>
</TR>
<TR><TD>CHRNA4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128169">GDB:128169</A></TD><TD>20q13.2-20q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118504">CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 4; CHRNA4</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121200">EPILEPSY, BENIGN NEONATAL; EBN1</A><BR>
</TD>
</TR>
<TR><TD>CST3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119817">GDB:119817</A></TD><TD>20p11.2-20p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105150">AMYLOIDOSIS VI</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604312"></A><BR>
</TD>
</TR>
<TR><TD>EDN3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119862">GDB:119862</A></TD><TD>20q13.2-20q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=131242">ENDOTHELIN-3; EDN3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=277580">WAARDENBURG-SHAH SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>EEGV1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127525">GDB:127525</A></TD><TD>20q13.2-20q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=130180">ELECTROENCEPHALOGRAM, LOW-VOLTAGE</A><BR>
</TD>
</TR>
<TR><TD>FTLL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119235">GDB:119235</A></TD><TD>20q12-20qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134790">FERRITIN LIGHT CHAIN; FTL</A><BR>
</TD>
</TR>
<TR><TD>GDF5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433948">GDB:433948</A></TD><TD>20q11.2-20q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=200700">CHONDRODYSPLASIA, GREBE TYPE</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601146">CARTILAGE-DERIVED MORPHOGENETIC PROTEIN 1</A><BR>
</TD>
</TR>
<TR><TD>GNAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120628">GDB:120628</A></TD><TD>20q13.2-20q13.3 20q13.2-20q13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=139320">GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-STIMULATING POLYPEPTIDE;</A><BR>
</TD>
</TR>
<TR><TD>GSS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:637022">GDB:637022</A></TD><TD>20q11.2-20q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231900">GLUTATHIONE SYNTHETASE DEFICIENCY OF ERYTHROCYTES, HEMOLYTIC ANEMIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=266130">PYROGLUTAMICACIDURIA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601002"></A><BR>
</TD>
</TR>
<TR><TD>HNF4A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:393281">GDB:393281</A></TD><TD>20q12-20q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=125850">DIABETES MELLITUS, AUTOSOMAL DOMINANT</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600281">TRANSCRIPTION FACTOR 14, HEPATIC NUCLEAR FACTOR; TCF14</A><BR>
</TD>
</TR>
<TR><TD>JAG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6175920">GDB:6175920</A></TD><TD>20p12-20p12 20p12.2-20p12.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=118450">CHOLESTASIS WITH PERIPHERAL PULMONARY STENOSIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601920">JAGGED 1; JAG1</A><BR>
</TD>
</TR>
<TR><TD>KCNQ2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9787229">GDB:9787229</A></TD><TD>20q13.3-20q13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=121200">EPILEPSY, BENIGN NEONATAL; EBN1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602235">POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY Q, MEMBER 2</A><BR>
</TD>
</TR>
<TR><TD>MKKS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9860197">GDB:9860197</A></TD><TD>20p12-20p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=236700">HYDROMETROCOLPOS SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>NBIA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4252819">GDB:4252819</A></TD><TD>20p13-20p12.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=234200">HALLERVORDEN-SPATZ DISEASE</A><BR>
</TD>
</TR>
<TR><TD>PCK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125349">GDB:125349</A></TD><TD>20q13.2-20q13.31 20q13.31-20q13.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261680">PHOSPHOENOLPYRUVATE CARBOXYKINASE 1, SOLUBLE; PCK1</A><BR>
</TD>
</TR>
<TR><TD>PI3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:203940">GDB:203940</A></TD><TD>20q12-20q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182257">PROTEINASE INHIBITOR 3; PI3</A><BR>
</TD>
</TR>
<TR><TD>PPCD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:702144">GDB:702144</A></TD><TD>20q11-20q11 20p11.2-20p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=122000">CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR; PPCD</A><BR>
</TD>
</TR>
<TR><TD>PPGB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119507">GDB:119507</A></TD><TD>20q13.1-20q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=256540">NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>PRNP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120720">GDB:120720</A></TD><TD>20pter-20p12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137440">GERSTMANN-STRAUSSLER DISEASE; GSD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176640">PRION PROTEIN; PRNP</A><BR>
</TD>
</TR>
<TR><TD>THBD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119613">GDB:119613</A></TD><TD>20p11.2-20p11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188040">THROMBOMODULIN; THBD</A><BR>
</TD>
</TR>
<TR><TD>TOP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120444">GDB:120444</A></TD><TD>20q11.2-20q13.1 20q12-20q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126420">TOPOISOMERASE (DNA) I; TOP1</A><BR>
</TD>
</TR>
<TR><TD>AIRE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:567198">GDB:567198</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=240300">AUTOIMMUNE POLYENDOCRINOPATHY-CANDIDIASIS-ECTODERMAL DYSTROPHY; APECED</A><BR>
</TD>
</TR>
<TR><TD>APP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119692">GDB:119692</A></TD><TD>21q21.2-21q21.2 21q21.3-21q21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104300">ALZHEIMER DISEASE; AD</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104760">AMYLOID BETA A4 PRECURSOR PROTEIN; APP</A><BR>
</TD>
</TR>
<TR><TD>CBS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119754">GDB:119754</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=236200">HOMOCYSTINURIA</A><BR>
</TD>
</TR>
<TR><TD>COL6A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119065">GDB:119065</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120220">COLLAGEN, TYPE VI, ALPHA-1 CHAIN; COL6A1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158810">MYOPATHY, BENIGN CONGENITAL, WITH CONTRACTURES</A><BR>
</TD>
</TR>
<TR><TD>COL6A2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119793">GDB:119793</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=120240">COLLAGEN, TYPE VI, ALPHA-2 CHAIN; COL6A2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158810">MYOPATHY, BENIGN CONGENITAL, WITH CONTRACTURES</A><BR>
</TD>
</TR>
<TR><TD>CSTB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5215249">GDB:5215249</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=254800">MYOCLONUS EPILEPSY OF UNVERRICHT AND LUNDBORG</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601145">CYSTATIN B; CSTB</A><BR>
</TD>
</TR>
<TR><TD>DCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125354">GDB:125354</A></TD><TD>21q22.2-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190685">TRISOMY 21</A><BR>
</TD>
</TR>
<TR><TD>DSCR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:731000">GDB:731000</A></TD><TD>21q22.1-21q22.2 21q22.12-21q22.12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190685">TRISOMY 21</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602917"></A><BR>
</TD>
</TR>
<TR><TD>FPDMM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954610">GDB:9954610</A></TD><TD>21q22.1-21q22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151385">CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 2; CBFA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601399">PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY</A><BR>
</TD>
</TR>
<TR><TD>HLCS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:392648">GDB:392648</A></TD><TD>21q22.1-21q22.1 21q22.2-21q22.2 21q22.13-21q22.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253270">MULTIPLE CARBOXYLASE DEFICIENCY, BIOTIN-RESPONSIVE; MCD</A><BR>
</TD>
</TR>
<TR><TD>HPE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136065">GDB:136065</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=236100">HOLOPROSENCEPHALY, FAMILIAL ALOBAR</A><BR>
</TD>
</TR>
<TR><TD>ITGB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120574">GDB:120574</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600065">INTEGRIN BETA-2; ITGB2</A><BR>
</TD>
</TR>
<TR><TD>KCNE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127909">GDB:127909</A></TD><TD>21q22.1-21q22.2 21q22.12-21q22.12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176261">POTASSIUM VOLTAGE-GATED CHANNEL, ISK-RELATED SUBFAMILY, MEMBER 1;</A><BR>
</TD>
</TR>
<TR><TD>KNO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4073044">GDB:4073044</A></TD><TD>21q22.3-21q22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=267750">KNOBLOCH SYNDROME; KNO</A><BR>
</TD>
</TR>
<TR><TD>PRSS7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:384083">GDB:384083</A></TD><TD>21q21-21q21 21q21.1-21q21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=226200">ENTEROKINASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>RUNX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128313">GDB:128313</A></TD><TD>21q22.1-21q22.1 21q22.1-21q22.2 21q22.12-21q22.12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151385">CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 2; CBFA2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601399">PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY</A><BR>
</TD>
</TR>
<TR><TD>SOD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119596">GDB:119596</A></TD><TD>21q22.1-21q22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=105400">AMYOTROPHIC LATERAL SCLEROSIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147450">SUPEROXIDE DISMUTASE-1; SOD1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=158700">MUSCULAR ATROPHY, PROGRESSIVE, WITH AMYOTROPHIC LATERAL SCLEROSIS</A><BR>
</TD>
</TR>
<TR><TD>TAM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958709">GDB:9958709</A></TD><TD>21q11.2-21q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=159595">MYELOPROLIFERATIVE SYNDROME, TRANSIENT</A><BR>
</TD>
</TR>
<TR><TD>ADSL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119655">GDB:119655</A></TD><TD>22q13.1-22q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=103050">ADENYLOSUCCINATE LYASE; ADSL</A><BR>
</TD>
</TR>
<TR><TD>ARSA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119007">GDB:119007</A></TD><TD>22q13.31-22qter 22q13.33-22q13.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250100">METACHROMATIC LEUKODYSTROPHY, LATE-INFANTILE</A><BR>
</TD>
</TR>
<TR><TD>BCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120562">GDB:120562</A></TD><TD>22q11.2-22q11.2 22q11.21-22q11.21 22q11-22q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151410">BREAKPOINT CLUSTER REGION;  BCR</A><BR>
</TD>
</TR>
<TR><TD>CECR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119772">GDB:119772</A></TD><TD>22pter-22q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115470">CAT EYE SYNDROME; CES</A><BR>
</TD>
</TR>
<TR><TD>CHEK2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958730">GDB:9958730</A></TD><TD>22q11-22q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=151623">LI-FRAUMENI SYNDROME; LFS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=259500">OSTEOGENIC SARCOMA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604373"></A><BR>
</TD>
</TR>
<TR><TD>COMT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119795">GDB:119795</A></TD><TD>22q11.21-22q11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=116790">CATECHOL-O-METHYLTRANSFERASE; COMT</A><BR>
</TD>
</TR>
<TR><TD>CRYBB2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119075">GDB:119075</A></TD><TD>22q11.2-22q12.1 22q11.2-22q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=123620">CRYSTALLIN, BETA B2; CRYBB2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601547">CATARACT, CONGENITAL, CERULEAN TYPE, 2; CCA2</A><BR>
</TD>
</TR>
<TR><TD>CSF2RB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126838">GDB:126838</A></TD><TD>22q12.3-22q13.1 22q13.1-22q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=138981">GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR RECEPTOR, BETA SUBUNIT;</A><BR>
</TD>
</TR>
<TR><TD>CTHM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439247">GDB:439247</A></TD><TD>22q11-22q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=217095">HEART MALFORMATIONS; CTHM</A><BR>
</TD>
</TR>
<TR><TD>CYP2D6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132127">GDB:132127</A></TD><TD>22q13.1-22q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=124030">CYTOCHROME P450, SUBFAMILY IID; CYP2D</A><BR>
</TD>
</TR>
<TR><TD>CYP2D7P1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119832">GDB:119832</A></TD><TD>22q13-22q13 22q13.1-22q13.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=124030">CYTOCHROME P450, SUBFAMILY IID; CYP2D</A><BR>
</TD>
</TR>
<TR><TD>DGCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119843">GDB:119843</A></TD><TD>22q11.21-22q11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188400">DIGEORGE SYNDROME; DGS</A><BR>
</TD>
</TR>
<TR><TD>DIA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119848">GDB:119848</A></TD><TD>22q13.31-22qter 22q13.31-22q13.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=250800">METHEMOGLOBINEMIA DUE TO DEFICIENCY OF METHEMOGLOBIN REDUCTASE</A><BR>
</TD>
</TR>
<TR><TD>EWSR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:135984">GDB:135984</A></TD><TD>22q12.1-22q12.3 22q12.1-22q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=133450">EWING SARCOMA; EWS</A><BR>
</TD>
</TR>
<TR><TD>GGT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120623">GDB:120623</A></TD><TD>22q11.2-22q12.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231950">GLUTATHIONURIA</A><BR>
</TD>
</TR>
<TR><TD>MGCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120180">GDB:120180</A></TD><TD>22q12.3-22qter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156100">MENINGIOMA; MGM</A><BR>
</TD>
</TR>
<TR><TD>MN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:580528">GDB:580528</A></TD><TD>22q11-22q11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=156100">MENINGIOMA; MGM</A><BR>
</TD>
</TR>
<TR><TD>NAGA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119445">GDB:119445</A></TD><TD>22q13-22qter 22q11-22q11 22q13.1-22q13.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=104170">ALPHA-GALACTOSIDASE B; GALB</A><BR>
</TD>
</TR>
<TR><TD>NF2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120232">GDB:120232</A></TD><TD>22q12.1-22q12.3 22q12.2-22q12.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=101000">NEUROFIBROMATOSIS, TYPE II; NF2</A><BR>
</TD>
</TR>
<TR><TD>OGS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954619">GDB:9954619</A></TD><TD>22q11.2-22q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145410">HYPERTELORISM WITH ESOPHAGEAL ABNORMALITY AND HYPOSPADIAS</A><BR>
</TD>
</TR>
<TR><TD>PDGFB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120709">GDB:120709</A></TD><TD>22q12.3-22q13.1 22q13.1-22q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=190040">V-SIS PLATELET-DERIVED GROWTH FACTOR BETA POLYPEPTIDE; PDGFB</A><BR>
</TD>
</TR>
<TR><TD>PPARA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:202877">GDB:202877</A></TD><TD>17p12-17p11.2 22q12-22q13.1 22q13.33-22q13.33 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=170998">PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR, ALPHA; PPARA</A><BR>
</TD>
</TR>
<TR><TD>PRODH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5215168">GDB:5215168</A></TD><TD>22q11.2-22q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=239500">HYPERPROLINEMIA, TYPE I</A><BR>
</TD>
</TR>
<TR><TD>SCO2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958568">GDB:9958568</A></TD><TD>22q13-22q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=220110">CYTOCHROME c OXIDASE DEFICIENCY</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604272"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604377"></A><BR>
</TD>
</TR>
<TR><TD>SCZD4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1387047">GDB:1387047</A></TD><TD>22q11-22q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600850">SCHIZOPHRENIA DISORDER-4; SCZD4</A><BR>
</TD>
</TR>
<TR><TD>SERPIND1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120038">GDB:120038</A></TD><TD>22q11.2-22q11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142360">HEPARIN COFACTOR II; HCF2</A><BR>
</TD>
</TR>
<TR><TD>SLC5A1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120375">GDB:120375</A></TD><TD>22q13.1-22q13.1 22q12.3-22q13.1 22q12.3-22q12.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=182380">SOLUTE CARRIER FAMILY 5, MEMBER 1; SLC5A1</A><BR>
</TD>
</TR>
<TR><TD>SOX10</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9834028">GDB:9834028</A></TD><TD>22q12-22q13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602229">SRY-BOX 10; SOX10</A><BR>
</TD>
</TR>
<TR><TD>TCN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119608">GDB:119608</A></TD><TD>22q12-22q13 22q12.1-22q12.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=275350">TRANSCOBALAMIN II DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>TIMP3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138175">GDB:138175</A></TD><TD>22q12.1-22q13.2 22q12.3-22q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=188826">TISSUE INHIBITOR OF METALLOPROTEINASE-3; TIMP3</A><BR>
</TD>
</TR>
<TR><TD>TST</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134043">GDB:134043</A></TD><TD>22q12.3-22q13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180370">RHODANESE; RDS</A><BR>
</TD>
</TR>
<TR><TD>VCF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136422">GDB:136422</A></TD><TD>22q11.2-22q11.2 22q11.21-22q11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=192430">VELOCARDIOFACIAL SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>AMELY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119676">GDB:119676</A></TD><TD>Yp11.2-Yp11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=410000">AMELOGENIN, Y-CHROMOSOMAL; AMELY</A><BR>
</TD>
</TR>
<TR><TD>ASSP6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119020">GDB:119020</A></TD><TD>Ypter-Yqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215700">CITRULLINEMIA</A><BR>
</TD>
</TR>
<TR><TD>AZF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119027">GDB:119027</A></TD><TD>Yq11-Yq11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=415000">AZOOSPERMIA FACTOR 1; AZF1</A><BR>
</TD>
</TR>
<TR><TD>AZF2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:456131">GDB:456131</A></TD><TD>Ycen-Yqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=400000">AZOOSPERMIA FACTOR 2; AZF2</A><BR>
</TD>
</TR>
<TR><TD>DAZ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:635890">GDB:635890</A></TD><TD>Yq11.22-Yq11.22 Yq12-Yq12 Yq11-Yq11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=400003">DELETED IN AZOOSPERMIA; DAZ</A><BR>
</TD>
</TR>
<TR><TD>GCY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119267">GDB:119267</A></TD><TD>Yq11-Yq11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=475000">CONTROL, Y-CHROMOSOME INFLUENCED; GCY</A><BR>
</TD>
</TR>
<TR><TD>RPS4Y</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128052">GDB:128052</A></TD><TD>Yp11.3-Yp11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=470000">RIBOSOMAL PROTEIN S4, Y-LINKED; RPS4Y</A><BR>
</TD>
</TR>
<TR><TD>SMCY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5875390">GDB:5875390</A></TD><TD>Ycen-Yq11.23 Ypter-Yqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=426000">HISTOCOMPATIBILITY Y ANTIGEN; HY; HYA</A><BR>
</TD>
</TR>
<TR><TD>SRY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125556">GDB:125556</A></TD><TD>Yp11.3-Yp11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=480000">SEX-DETERMINING REGION Y; SRY</A><BR>
</TD>
</TR>
<TR><TD>ZFY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120503">GDB:120503</A></TD><TD>Yp11.3-Yp11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=490000">ZINC FINGER PROTEIN, Y-LINKED; ZFY</A><BR>
</TD>
</TR>
<TR><TD>ABCD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118991">GDB:118991</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300100">ADRENOLEUKODYSTROPHY; ALD</A><BR>
</TD>
</TR>
<TR><TD>ACTL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119648">GDB:119648</A></TD><TD>Xp11.22-Xp11.21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300020">ACTIN-LIKE SEQUENCE-1; ACTL1</A><BR>
</TD>
</TR>
<TR><TD>ADFN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118977">GDB:118977</A></TD><TD>Xq25-Xq26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300700">ALBINISM-DEAFNESS SYNDROME; ADFN; ALDS</A><BR>
</TD>
</TR>
<TR><TD>AGMX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119661">GDB:119661</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300310">AGAMMAGLOBULINEMIA, X-LINKED, TYPE 2; AGMX2; XLA2</A><BR>
</TD>
</TR>
<TR><TD>AHDS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125899">GDB:125899</A></TD><TD>Xq21.1-Xq21.1 Xq21-Xq21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309600">MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA</A><BR>
</TD>
</TR>
<TR><TD>AIC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118986">GDB:118986</A></TD><TD>Xp22-Xp22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304050">CORPUS CALLOSUM, AGENESIS OF, WITH CHORIORETINAL ABNORMALITY</A><BR>
</TD>
</TR>
<TR><TD>AIED</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119663">GDB:119663</A></TD><TD>Xp11.4-Xq21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300600">ALBINISM, OCULAR, TYPE 2; OA2</A><BR>
</TD>
</TR>
<TR><TD>AIH3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131443">GDB:131443</A></TD><TD>Xq22-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301201">AMELOGENESIS IMPERFECTA-3, HYPOPLASTIC TYPE; AIH3</A><BR>
</TD>
</TR>
<TR><TD>ALAS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119666">GDB:119666</A></TD><TD>Xp11.21-Xp11.21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301300">ANEMIA, HYPOCHROMIC</A><BR>
</TD>
</TR>
<TR><TD>AMCD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5584286">GDB:5584286</A></TD><TD>Xp11.3-Xq11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301830">ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL</A><BR>
</TD>
</TR>
<TR><TD>AMELX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119675">GDB:119675</A></TD><TD>Xp22.31-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301200">AMELOGENESIS IMPERFECTA-1, HYPOPLASTIC TYPE; AIH1</A><BR>
</TD>
</TR>
<TR><TD>ANOP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128454">GDB:128454</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301590">CLINICAL; ANOP1</A><BR>
</TD>
</TR>
<TR><TD>AR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120556">GDB:120556</A></TD><TD>Xq11.2-Xq12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300068">ANDROGEN INSENSITIVITY SYNDROME; AIS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313700">ANDROGEN RECEPTOR; AR</A><BR>
</TD>
</TR>
<TR><TD>ARAF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119004">GDB:119004</A></TD><TD>Xp11.3-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311010">V-RAF MURINE SARCOMA 3611 VIRAL ONCOGENE HOMOLOG 1; ARAF1</A><BR>
</TD>
</TR>
<TR><TD>ARSC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119702">GDB:119702</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301780">ARYLSULFATASE C, f FORM; ARSC2</A><BR>
</TD>
</TR>
<TR><TD>ARSE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:555743">GDB:555743</A></TD><TD>Xp22.3-Xp22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302950">CHONDRODYSPLASIA PUNCTATA 1, X-LINKED RECESSIVE;  CDPX1</A><BR>
</TD>
</TR>
<TR><TD>ARTS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954651">GDB:9954651</A></TD><TD>Xq21.2-Xq24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301835">FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION</A><BR>
</TD>
</TR>
<TR><TD>ARX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128367">GDB:128367</A></TD><TD>Xpter-Xp21 Xp22.12-Xp22.12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300382"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308350">SPASMS, X-LINKED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309510">PARTINGTON X-LINKED MENTAL RETARDATION SYNDROME; PRTS</A><BR>
</TD>
</TR>
<TR><TD>ASAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954649">GDB:9954649</A></TD><TD>Xq13-Xq13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301310">SIDEROBLASTIC, AND SPINOCEREBELLAR ATAXIA; ASAT</A><BR>
</TD>
</TR>
<TR><TD>ASSP5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119019">GDB:119019</A></TD><TD>Xq22-Xq26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=215700">CITRULLINEMIA</A><BR>
</TD>
</TR>
<TR><TD>ATP7A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119395">GDB:119395</A></TD><TD>Xq13.2-Xq13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300011">ATPase, Cu(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309400">MENKES SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>ATRX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136052">GDB:136052</A></TD><TD>Xq13.3-Xq13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300032">ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301040">ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, NONDELETION TYPE</A><BR>
</TD>
</TR>
<TR><TD>AVPR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131475">GDB:131475</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304800">DIABETES INSIPIDUS, NEPHROGENIC</A><BR>
</TD>
</TR>
<TR><TD>BFLS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120566">GDB:120566</A></TD><TD>Xq26-Xq27.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301900">BORJESON SYNDROME; BORJ</A><BR>
</TD>
</TR>
<TR><TD>BGN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119727">GDB:119727</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301870">BIGLYCAN; BGN</A><BR>
</TD>
</TR>
<TR><TD>BTK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120542">GDB:120542</A></TD><TD>Xq21.33-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300300">BRUTON AGAMMAGLOBULINEMIA TYROSINE KINASE; BTK</A><BR>
</TD>
</TR>
<TR><TD>BZX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5205912">GDB:5205912</A></TD><TD>Xq24-Xq27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301845">BAZEX SYNDROME; BZX</A><BR>
</TD>
</TR>
<TR><TD>C1HR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119040">GDB:119040</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313650">TATA BOX BINDING PROTEIN (TBP)-ASSOCIATED FACTOR 2A; TAF2A</A><BR>
</TD>
</TR>
<TR><TD>CACNA1F</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6053864">GDB:6053864</A></TD><TD>Xp11.23-Xp11.22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300071">NIGHTBLINDNESS, CONGENITAL STATIONARY, X-LINKED, TYPE 2; CSNB2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300110">CALCIUM CHANNEL, VOLTAGE-DEPENDENT, ALPHA 1F SUBUNIT; CACNA1F</A><BR>
</TD>
</TR>
<TR><TD>CALB3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:133780">GDB:133780</A></TD><TD>Xp22.2-Xp22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302020">CALBINDIN 3; CALB3</A><BR>
</TD>
</TR>
<TR><TD>CBBM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958963">GDB:9958963</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303700">COLORBLINDNESS, BLUE-MONO-CONE-MONOCHROMATIC TYPE; CBBM</A><BR>
</TD>
</TR>
<TR><TD>CCT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119756">GDB:119756</A></TD><TD>Xpter-Xqter Xpter-Xcen </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302200">CATARACT, CONGENITAL TOTAL, WITH POSTERIOR SUTURAL OPACITIES IN HETEROZYGOTES;</A><BR>
</TD>
</TR>
<TR><TD>CDR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119053">GDB:119053</A></TD><TD>Xq27.1-Xq27.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302650">CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN-1; CDR1; CDR34</A><BR>
</TD>
</TR>
<TR><TD>CFNS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9579470">GDB:9579470</A></TD><TD>Xp22-Xp22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304110">CRANIOFRONTONASAL SYNDROME; CFNS</A><BR>
</TD>
</TR>
<TR><TD>CGF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6275867">GDB:6275867</A></TD><TD>Xp11.22-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300082">COGNITION</A><BR>
</TD>
</TR>
<TR><TD>CHM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120400">GDB:120400</A></TD><TD>Xq21.1-Xq21.2 Xq21.2-Xq21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303100">CHOROIDEREMIA; CHM</A><BR>
</TD>
</TR>
<TR><TD>CHR39C</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119779">GDB:119779</A></TD><TD>Xq13-Xq21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302920">CHOLESTEROL REPRESSIBLE PROTEIN 39C; CHR39C</A><BR>
</TD>
</TR>
<TR><TD>CIDX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127736">GDB:127736</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312863">SEVERE COMBINED IMMUNODEFICIENCY DISEASE, X-LINKED, 2; SCIDX2</A><BR>
</TD>
</TR>
<TR><TD>CLA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119782">GDB:119782</A></TD><TD>Xq23-Xq24 Xpter-Xqter Xp11.21-Xq21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302500">CEREBELLAR ATAXIA, X-LINKED; CLA2</A><BR>
</TD>
</TR>
<TR><TD>CLCN5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:270667">GDB:270667</A></TD><TD>Xp11.23-Xp11.22 Xp11.22-Xp11.22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300008">CHLORIDE CHANNEL 5; CLCN5</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300009">FANCONI SYNDROME, RENAL, WITH NEPHROCALCINOSIS AND RENAL STONES</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310468">NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE; XRN</A><BR>
</TD>
</TR>
<TR><TD>CLS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119784">GDB:119784</A></TD><TD>Xp22.2-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300075">RIBOSOMAL PROTEIN S6 KINASE, 90 KD, POLYPEPTIDE 3; RPS6KA3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303600">COFFIN-LOWRY SYNDROME; CLS</A><BR>
</TD>
</TR>
<TR><TD>CMTX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128311">GDB:128311</A></TD><TD>Xp22-Xp22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302801">CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 2; CMTX2</A><BR>
</TD>
</TR>
<TR><TD>CMTX3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128151">GDB:128151</A></TD><TD>Xq26-Xq26 Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302802">CHARCOT-MARIE-TOOTH NEUROPATHY, X-LINKED RECESSIVE, 3; CMTX3</A><BR>
</TD>
</TR>
<TR><TD>CND</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954627">GDB:9954627</A></TD><TD>Xp22.2-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304730">DERMOIDS OF CORNEA; CND</A><BR>
</TD>
</TR>
<TR><TD>COD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119787">GDB:119787</A></TD><TD>Xp11.4-Xp11.4 Xp21.1-Xp11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304020">CONE DYSTROPHY, X-LINKED, 1; COD1</A><BR>
</TD>
</TR>
<TR><TD>COD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6520166">GDB:6520166</A></TD><TD>Xq27-Xq27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300085">CONE DYSTROPHY, X-LINKED, 2; COD2</A><BR>
</TD>
</TR>
<TR><TD>COL4A5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120596">GDB:120596</A></TD><TD>Xq22-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303630">COLLAGEN, TYPE IV, ALPHA-5 CHAIN; COL4A5</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308940">LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY</A><BR>
</TD>
</TR>
<TR><TD>COL4A6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:222775">GDB:222775</A></TD><TD>Xq22-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303631">COLLAGEN, TYPE IV, ALPHA-6 CHAIN; COL4A6</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308940">LEIOMYOMATOSIS, ESOPHAGEAL AND VULVAL, WITH NEPHROPATHY</A><BR>
</TD>
</TR>
<TR><TD>CPX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120598">GDB:120598</A></TD><TD>Xq21.3-Xq22 Xq21.3-Xq21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303400">CLEFT PALATE, X-LINKED; CPX</A><BR>
</TD>
</TR>
<TR><TD>CVD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954659">GDB:9954659</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314400">CARDIAC VALVULAR DYSPLASIA, X-LINKED</A><BR>
</TD>
</TR>
<TR><TD>CYBB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120513">GDB:120513</A></TD><TD>Xp21.1-Xp21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306400">GRANULOMATOUS DISEASE, CHRONIC; CGD</A><BR>
</TD>
</TR>
<TR><TD>DCX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9823272">GDB:9823272</A></TD><TD>Xq22.3-Xq23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300067">LISSENCEPHALY, X-LINKED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300121"></A><BR>
</TD>
</TR>
<TR><TD>DFN2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119091">GDB:119091</A></TD><TD>Xq22-Xq22 Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304500">DEAFNESS, X-LINKED 2, PERCEPTIVE CONGENITAL; DFN2</A><BR>
</TD>
</TR>
<TR><TD>DFN4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433255">GDB:433255</A></TD><TD>Xp21.2-Xp21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300030">DEAFNESS, X-LINKED 4, CONGENITAL SENSORINEURAL; DFN4</A><BR>
</TD>
</TR>
<TR><TD>DFN6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1320698">GDB:1320698</A></TD><TD>Xp22-Xp22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300066">DEAFNESS, X-LINKED, 6, PROGRESSIVE; DFN6</A><BR>
</TD>
</TR>
<TR><TD>DHOF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119847">GDB:119847</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305600">FOCAL DERMAL HYPOPLASIA; DHOF</A><BR>
</TD>
</TR>
<TR><TD>DIAPH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9835484">GDB:9835484</A></TD><TD>Xq21-Xq21 Xq22-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300108">DIAPHANOUS, DROSOPHILA, HOMOLOG OF, 2</A><BR>
</TD>
</TR>
<TR><TD>DKC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119096">GDB:119096</A></TD><TD>Xq27-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300126"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305000">DYSKERATOSIS CONGENITA; DKC</A><BR>
</TD>
</TR>
<TR><TD>DMD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119850">GDB:119850</A></TD><TD>Xp21.3-Xp21.2 Xp21.2-Xp21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300376"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300377"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310200">MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKER</A><BR>
</TD>
</TR>
<TR><TD>DSS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433750">GDB:433750</A></TD><TD>Xp21.3-Xp21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300018">DOSAGE-SENSITIVE SEX REVERSAL; DSS</A><BR>
</TD>
</TR>
<TR><TD>DYT3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118789">GDB:118789</A></TD><TD>Xq12-Xq13.1 Xq13.1-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314250">TORSION DYSTONIA-3, X-LINKED TYPE; DYT3</A><BR>
</TD>
</TR>
<TR><TD>EBM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119102">GDB:119102</A></TD><TD>Xpter-Xqter Xq27.3-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302000">BULLOUS DYSTROPHY, HEREDITARY MACULAR TYPE</A><BR>
</TD>
</TR>
<TR><TD>EBP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125212">GDB:125212</A></TD><TD>Xpter-Xqter Xp22-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300205"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302960">CHONDRODYSPLASIA PUNCTATA, X-LINKED DOMINANT; CDPX2; CDPXD; CPXD</A><BR>
</TD>
</TR>
<TR><TD>ED1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119859">GDB:119859</A></TD><TD>Xq12-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305100">ECTODERMAL DYSPLASIA, ANHIDROTIC; EDA</A><BR>
</TD>
</TR>
<TR><TD>ELK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119867">GDB:119867</A></TD><TD>Xp11.3-Xp11.23 Xp11.2-Xp11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311040">ELK1, MEMBER OF ETS ONCOGENE FAMILY; ELK1</A><BR>
</TD>
</TR>
<TR><TD>EMD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119108">GDB:119108</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310300">MUSCULAR DYSTROPHY, TARDIVE, DREIFUSS-EMERY TYPE, WITH CONTRACTURES</A><BR>
</TD>
</TR>
<TR><TD>EVR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136068">GDB:136068</A></TD><TD>Xp11.4-Xp11.3 Xp11-Xp11 Xq21.3-Xq21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305390">EXUDATIVE VITREORETINOPATHY, FAMILIAL, X-LINKED RECESSIVE; EVR2</A><BR>
</TD>
</TR>
<TR><TD>F8</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119124">GDB:119124</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305424">FACTOR VIII ASSOCIATED GENE 2</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306700">HEMOPHILIA A</A><BR>
</TD>
</TR>
<TR><TD>F9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119900">GDB:119900</A></TD><TD>Xq26.3-Xq27.1 Xq27.1-Xq27.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306900">HEMOPHILIA B; HEMB</A><BR>
</TD>
</TR>
<TR><TD>FCP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:347490">GDB:347490</A></TD><TD>Xp22.3-Xp22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305435">F-CELL PRODUCTION, X-LINKED; FCPX</A><BR>
</TD>
</TR>
<TR><TD>FDPSL5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119922">GDB:119922</A></TD><TD>Xq21-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305425">SYNTHETASE-5; FPSL5</A><BR>
</TD>
</TR>
<TR><TD>FGD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119131">GDB:119131</A></TD><TD>Xp11.21-Xp11.21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100050">SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305400">FACIOGENITAL DYSPLASIA; FGDY</A><BR>
</TD>
</TR>
<TR><TD>FGS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9836950">GDB:9836950</A></TD><TD>Xq12-Xq21.31 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305450">FG SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>FMR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:129038">GDB:129038</A></TD><TD>Xq27.3-Xq27.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309550">FRAGILE SITE MENTAL RETARDATION-1; FMR1</A><BR>
</TD>
</TR>
<TR><TD>FMR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:141566">GDB:141566</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309548">FRAGILE SITE, FOLIC ACID TYPE, RARE, FRA(X)(q28); FRAXE</A><BR>
</TD>
</TR>
<TR><TD>G6PD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120621">GDB:120621</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305900">GLUCOSE-6-PHOSPHATE DEHYDROGENASE; G6PD</A><BR>
</TD>
</TR>
<TR><TD>GABRA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119968">GDB:119968</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305660">GAMMA-AMINOBUTYRIC ACID RECEPTOR, ALPHA-3; GABRA3</A><BR>
</TD>
</TR>
<TR><TD>GATA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125373">GDB:125373</A></TD><TD>Xp11.23-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305371">GATA-BINDING PROTEIN 1; GATA1</A><BR>
</TD>
</TR>
<TR><TD>GDI1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1347097">GDB:1347097</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300104">GDP DISSOCIATION INHIBITOR 1; GDI1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309541">MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 3; MRX3</A><BR>
</TD>
</TR>
<TR><TD>GDXY</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954629">GDB:9954629</A></TD><TD>Xp22.11-Xp21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306100">DYSGENESIS, XY FEMALE TYPE; GDXY</A><BR>
</TD>
</TR>
<TR><TD>GJB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125246">GDB:125246</A></TD><TD>Xq13.1-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302800">CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED; CMTX1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304040">GAP JUNCTION PROTEIN, BETA-1, 32 KD; GJB1</A><BR>
</TD>
</TR>
<TR><TD>GK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119271">GDB:119271</A></TD><TD>Xp21.3-Xp21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=307030">HYPERGLYCEROLEMIA</A><BR>
</TD>
</TR>
<TR><TD>GLA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119272">GDB:119272</A></TD><TD>Xq21.3-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301500">ANGIOKERATOMA, DIFFUSE</A><BR>
</TD>
</TR>
<TR><TD>GPC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3770726">GDB:3770726</A></TD><TD>Xq26.1-Xq26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300037">GLYPICAN-3; GPC3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312870">SIMPSON DYSMORPHIA SYNDROME; SDYS</A><BR>
</TD>
</TR>
<TR><TD>GRPR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128035">GDB:128035</A></TD><TD>Xp22.2-Xp22.13 Xp22.2-Xp22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305670">GASTRIN-RELEASING PEPTIDE RECEPTOR; GRPR</A><BR>
</TD>
</TR>
<TR><TD>GTD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954635">GDB:9954635</A></TD><TD>Xp21-Xp21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306190">GONADOTROPIN DEFICIENCY; GTD</A><BR>
</TD>
</TR>
<TR><TD>GUST</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954655">GDB:9954655</A></TD><TD>Xq26-Xq26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309555">MENTAL RETARDATION WITH OPTIC ATROPHY, DEAFNESS, AND SEIZURES</A><BR>
</TD>
</TR>
<TR><TD>HMS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:251827">GDB:251827</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306995">1; HMS1</A><BR>
</TD>
</TR>
<TR><TD>HPRT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119317">GDB:119317</A></TD><TD>Xq26.1-Xq26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308000">HYPOXANTHINE GUANINE PHOSPHORIBOSYLTRANSFERASE 1; HPRT1</A><BR>
</TD>
</TR>
<TR><TD>HPT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119322">GDB:119322</A></TD><TD>Xq26-Xq27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=307700">HYPOPARATHYROIDISM, X-LINKED; HYPX</A><BR>
</TD>
</TR>
<TR><TD>HTC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:700980">GDB:700980</A></TD><TD>Xq24-Xq27.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=307150">HYPERTRICHOSIS, CONGENITAL GENERALIZED; CGH; HCG</A><BR>
</TD>
</TR>
<TR><TD>HTR2C</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:378202">GDB:378202</A></TD><TD>Xq24-Xq24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312861">5-@HYDROXYTRYPTAMINE RECEPTOR 2C; HTR2C</A><BR>
</TD>
</TR>
<TR><TD>HYR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954625">GDB:9954625</A></TD><TD>Xp22.3-Xp22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306970">REGULATOR; HYR</A><BR>
</TD>
</TR>
<TR><TD>IDS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120521">GDB:120521</A></TD><TD>Xq27.3-Xq28 Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309900">MUCOPOLYSACCHARIDOSIS TYPE II</A><BR>
</TD>
</TR>
<TR><TD>IHG1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119343">GDB:119343</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308500">HYPOPLASIA OF, WITH GLAUCOMA; IHG</A><BR>
</TD>
</TR>
<TR><TD>IL2RG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:134807">GDB:134807</A></TD><TD>Xq13.1-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308380">INTERLEUKIN-2 RECEPTOR, GAMMA; IL2RG</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312863">SEVERE COMBINED IMMUNODEFICIENCY DISEASE, X-LINKED, 2; SCIDX2</A><BR>
</TD>
</TR>
<TR><TD>INDX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954657">GDB:9954657</A></TD><TD>Xq26-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300076">IMMUNONEUROLOGIC DISORDER, X-LINKED</A><BR>
</TD>
</TR>
<TR><TD>IP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120105">GDB:120105</A></TD><TD>Xp11.21-Xcen </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308300">INCONTINENTIA PIGMENTI, TYPE I; IP1</A><BR>
</TD>
</TR>
<TR><TD>IP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120106">GDB:120106</A></TD><TD>Xq27-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308310">INCONTINENTIA PIGMENTI, TYPE II; IP2</A><BR>
</TD>
</TR>
<TR><TD>JMS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:204055">GDB:204055</A></TD><TD>Xq12-Xq21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309590">MENTAL RETARDATION, X-LINKED, WITH GROWTH RETARDATION, DEAFNESS, AND</A><BR>
</TD>
</TR>
<TR><TD>KAL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120116">GDB:120116</A></TD><TD>Xp22.32-Xp22.32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308700">KALLMANN SYNDROME 1; KAL1</A><BR>
</TD>
</TR>
<TR><TD>KFSD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128174">GDB:128174</A></TD><TD>Xp22.2-Xp21.2 Xp22.2-Xp22.13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308800">KERATOSIS FOLLICULARIS SPINULOSA DECALVANS CUM OPHIASI; KFSD</A><BR>
</TD>
</TR>
<TR><TD>L1CAM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120133">GDB:120133</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303350">CLASPED THUMB AND MENTAL RETARDATION</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308840">L1 CELL ADHESION MOLECULE; L1CAM</A><BR>
</TD>
</TR>
<TR><TD>LAMP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125376">GDB:125376</A></TD><TD>Xq24-Xq24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309060">LYSOSOME-ASSOCIATED MEMBRANE PROTEIN B; LAMP2; LAMPB</A><BR>
</TD>
</TR>
<TR><TD>MAA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119372">GDB:119372</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309800">MICROPHTHALMIA OR ANOPHTHALMOS, WITH ASSOCIATED ANOMALIES; MAA</A><BR>
</TD>
</TR>
<TR><TD>MAFD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119373">GDB:119373</A></TD><TD>Xq27-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309200">PSYCHOSIS, X-LINKED</A><BR>
</TD>
</TR>
<TR><TD>MAOA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120164">GDB:120164</A></TD><TD>Xp11.4-Xp11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309850">MONOAMINE OXIDASE A; MAOA</A><BR>
</TD>
</TR>
<TR><TD>MAOB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119377">GDB:119377</A></TD><TD>Xp11.4-Xp11.3 Xp11.23-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309860">MONOAMINE OXIDASE B; MAOB</A><BR>
</TD>
</TR>
<TR><TD>MCF2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120168">GDB:120168</A></TD><TD>Xq26.3-Xq27.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311030">MCF.2 CELL LINE DERIVED TRANSFORMING SEQUENCE; MCF2</A><BR>
</TD>
</TR>
<TR><TD>MCS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128370">GDB:128370</A></TD><TD>Xq13-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309605">MENTAL RETARDATION, X-LINKED, SYNDROMIC-4, WITH CONGENITAL CONTRACTURES</A><BR>
</TD>
</TR>
<TR><TD>MEAX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119383">GDB:119383</A></TD><TD>Xq28-Xq28 Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310440">X-LINKED, WITH EXCESSIVE AUTOPHAGY; XMEA; MEAX</A><BR>
</TD>
</TR>
<TR><TD>MECP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3851454">GDB:3851454</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300005"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312750">SYNDROME; RTT</A><BR>
</TD>
</TR>
<TR><TD>MF4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119386">GDB:119386</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309630">METACARPAL 4-5 FUSION; MF4</A><BR>
</TD>
</TR>
<TR><TD>MGC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120179">GDB:120179</A></TD><TD>Xq13.3-Xq25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309300">MEGALOCORNEA; MGC1; MGCN</A><BR>
</TD>
</TR>
<TR><TD>MIC5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120526">GDB:120526</A></TD><TD>Xq27-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313450">SURFACE ANTIGEN, X-LINKED; SAX</A><BR>
</TD>
</TR>
<TR><TD>MID1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9772232">GDB:9772232</A></TD><TD>Xp22-Xp22 Xp22.3-Xp22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300000">OPITZ SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300122"></A><BR>
</TD>
</TR>
<TR><TD>MLLT7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:392309">GDB:392309</A></TD><TD>Xq13-Xq13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300033">MYELOID/LYMPHOID OR MIXED-LINEAGE LEUKEMIA, TRANSLOCATED TO, 7; MLLT7</A><BR>
</TD>
</TR>
<TR><TD>MLS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:262123">GDB:262123</A></TD><TD>Xp22-Xp22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309801">MICROPHTHALMIA WITH LINEAR SKIN DEFECTS; MLS</A><BR>
</TD>
</TR>
<TR><TD>MRSD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119398">GDB:119398</A></TD><TD>Xq27-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309620">MENTAL RETARDATION, SKELETAL DYSPLASIA, AND ABDUCENS PALSY; MRSD</A><BR>
</TD>
</TR>
<TR><TD>MRX14</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138453">GDB:138453</A></TD><TD>Xp11-Xq13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300062">RETARDATION, X-LINKED 14; MRX14</A><BR>
</TD>
</TR>
<TR><TD>MRX1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120193">GDB:120193</A></TD><TD>Xp11-Xq13 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309530">MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 1; MRX1</A><BR>
</TD>
</TR>
<TR><TD>MRX20</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:217050">GDB:217050</A></TD><TD>Xp11.3-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300047">MENTAL RETARDATION, X-LINKED 20; MRX20</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600704"></A><BR>
</TD>
</TR>
<TR><TD>MRX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120194">GDB:120194</A></TD><TD>Xp22.3-Xp22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309540">RETARDATION, X-LINKED NONSPECIFIC, TYPE 2; MRX2</A><BR>
</TD>
</TR>
<TR><TD>MRX3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128105">GDB:128105</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300104">GDP DISSOCIATION INHIBITOR 1; GDI1</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309541">MENTAL RETARDATION, X-LINKED NONSPECIFIC, TYPE 3; MRX3</A><BR>
</TD>
</TR>
<TR><TD>MRX40</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:700754">GDB:700754</A></TD><TD>Xq21.1-Xq21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309600">MENTAL RETARDATION, X-LINKED, WITH HYPOTONIA</A><BR>
</TD>
</TR>
<TR><TD>MRXA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954641">GDB:9954641</A></TD><TD>Xp11-Xp11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309545">MENTAL RETARDATION, X-LINKED NONSPECIFIC, WITH APHASIA; MRXA</A><BR>
</TD>
</TR>
<TR><TD>MSD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119399">GDB:119399</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311400">SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>MTM1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119439">GDB:119439</A></TD><TD>Xq27.3-Xq28 Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310400">MYOTUBULAR MYOPATHY 1; MTM1</A><BR>
</TD>
</TR>
<TR><TD>MYCL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120209">GDB:120209</A></TD><TD>Xq22-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310310">MYCL-RELATED PROCESSED GENE; MYCL2</A><BR>
</TD>
</TR>
<TR><TD>MYP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127783">GDB:127783</A></TD><TD>Xpter-Xqter Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310460">MYOPIA, X-LINKED; MYP1</A><BR>
</TD>
</TR>
<TR><TD>NDP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119449">GDB:119449</A></TD><TD>Xp11.4-Xp11.3 Xp11.4-Xp11.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310600">NORRIE DISEASE; NDP</A><BR>
</TD>
</TR>
<TR><TD>NHS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120235">GDB:120235</A></TD><TD>Xp22.3-Xp21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302350">CATARACT-DENTAL SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>NPHL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433705">GDB:433705</A></TD><TD>Xp11.4-Xp11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310468">NEPHROLITHIASIS, X-LINKED RECESSIVE, WITH RENAL FAILURE; XRN</A><BR>
</TD>
</TR>
<TR><TD>NR0B1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118982">GDB:118982</A></TD><TD>Xp21.3-Xp21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300200">ADRENAL HYPOPLASIA, CONGENITAL; AHC</A><BR>
</TD>
</TR>
<TR><TD>NSX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125596">GDB:125596</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310465">SYNDROME; NSX</A><BR>
</TD>
</TR>
<TR><TD>NYS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119458">GDB:119458</A></TD><TD>Xpter-Xqter Xq26-Xq27 Xp11.4-Xp11.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310700">NYSTAGMUS, X-LINKED; NYS</A><BR>
</TD>
</TR>
<TR><TD>NYX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119814">GDB:119814</A></TD><TD>Xp11.4-Xp11.23 Xp11.3-Xp11.3 Xp11.4-Xp11.4 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300278"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310500">NIGHTBLINDNESS, CONGENITAL STATIONARY, WITH MYOPIA; CSNB1</A><BR>
</TD>
</TR>
<TR><TD>OA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119459">GDB:119459</A></TD><TD>Xp22.3-Xp22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300500">ALBINISM, OCULAR, TYPE 1; OA1</A><BR>
</TD>
</TR>
<TR><TD>OASD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138457">GDB:138457</A></TD><TD>Xp22.3-Xp22.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300650">OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS; OASD</A><BR>
</TD>
</TR>
<TR><TD>OCRL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119461">GDB:119461</A></TD><TD>Xq25-Xq26.1 Xq26.1-Xq26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309000">LOWE OCULOCEREBRORENAL SYNDROME; OCRL</A><BR>
</TD>
</TR>
<TR><TD>ODT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125360">GDB:125360</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313500">TEETH, ABSENCE OF</A><BR>
</TD>
</TR>
<TR><TD>OFD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120248">GDB:120248</A></TD><TD>Xp22.3-Xp22.2 Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300170"></A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311200">OROFACIODIGITAL SYNDROME 1; OFD1</A><BR>
</TD>
</TR>
<TR><TD>OPA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125358">GDB:125358</A></TD><TD>Xpter-Xqter Xp11.4-Xp11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311050">OPTIC ATROPHY 2; OPA2</A><BR>
</TD>
</TR>
<TR><TD>OPD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120249">GDB:120249</A></TD><TD>Xq26-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311300">OTOPALATODIGITAL SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>OPEM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119467">GDB:119467</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311000">OPHTHALMOPLEGIA, EXTERNAL, AND MYOPIA; OPEM</A><BR>
</TD>
</TR>
<TR><TD>OPN1LW</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120724">GDB:120724</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303900">COLORBLINDNESS, PARTIAL, PROTAN SERIES; CBP</A><BR>
</TD>
</TR>
<TR><TD>OPN1MW</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120622">GDB:120622</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303800">COLORBLINDNESS, PARTIAL, DEUTAN SERIES; CBD; DCB</A><BR>
</TD>
</TR>
<TR><TD>OTC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119468">GDB:119468</A></TD><TD>Xp21.1-Xp21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311250">ORNITHINE TRANSCARBAMYLASE DEFICIENCY, HYPERAMMONEMIA DUE TO; OTC</A><BR>
</TD>
</TR>
<TR><TD>P3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954667">GDB:9954667</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312090">PROTEIN P3</A><BR>
</TD>
</TR>
<TR><TD>PDHA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118895">GDB:118895</A></TD><TD>Xp22.1-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312170">PYRUVATE DEHYDROGENASE COMPLEX, E1-ALPHA POLYPEPTIDE-1; PDHA1</A><BR>
</TD>
</TR>
<TR><TD>PDR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:203409">GDB:203409</A></TD><TD>Xp22-Xp21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301220">AMYLOIDOSIS, FAMILIAL CUTANEOUS</A><BR>
</TD>
</TR>
<TR><TD>PFC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120275">GDB:120275</A></TD><TD>Xp11.3-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312060">PROPERDIN DEFICIENCY, X-LINKED</A><BR>
</TD>
</TR>
<TR><TD>PFKFB1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125375">GDB:125375</A></TD><TD>Xcen-Xq13 Xpter-Xqter Xp11.21-Xp11.21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311790">6-@PHOSPHOFRUCTO-2-KINASE; PFKFB1</A><BR>
</TD>
</TR>
<TR><TD>PGK1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120282">GDB:120282</A></TD><TD>Xq13.3-Xq13.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311800">PHOSPHOGLYCERATE KINASE 1; PGK1</A><BR>
</TD>
</TR>
<TR><TD>PGK1P1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120283">GDB:120283</A></TD><TD>Xq11.2-Xq12 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311800">PHOSPHOGLYCERATE KINASE 1; PGK1</A><BR>
</TD>
</TR>
<TR><TD>PGS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128372">GDB:128372</A></TD><TD>Xq25-Xq27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304340">DANDY-WALKER MALFORMATION WITH MENTAL RETARDATION, BASAL GANGLIA DISEASE,</A><BR>
</TD>
</TR>
<TR><TD>PHEX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120520">GDB:120520</A></TD><TD>Xp22.2-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=307800">HYPOPHOSPHATEMIA, VITAMIN D-RESISTANT RICKETS; HYP</A><BR>
</TD>
</TR>
<TR><TD>PHKA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120285">GDB:120285</A></TD><TD>Xq13.1-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311870">PHOSPHORYLASE KINASE, ALPHA 1 SUBUNIT (MUSCLE); PHKA1</A><BR>
</TD>
</TR>
<TR><TD>PHKA2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127279">GDB:127279</A></TD><TD>Xp22.2-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306000">GLYCOGEN STORAGE DISEASE VIII</A><BR>
</TD>
</TR>
<TR><TD>PHP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119494">GDB:119494</A></TD><TD>Xp21.1-Xp11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312000">PANHYPOPITUITARISM; PHP</A><BR>
</TD>
</TR>
<TR><TD>PIGA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:138138">GDB:138138</A></TD><TD>Xp22.1-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311770">PHOSPHATIDYLINOSITOL GLYCAN, CLASS A; PIGA</A><BR>
</TD>
</TR>
<TR><TD>PLP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120302">GDB:120302</A></TD><TD>Xq22-Xq22 Xq21.33-Xq22 Xq22.1-Xq22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312080">PROTEOLIPID PROTEIN, MYELIN; PLP</A><BR>
</TD>
</TR>
<TR><TD>POF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120716">GDB:120716</A></TD><TD>Xq26.1-Xq27 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311360">PREMATURE OVARIAN FAILURE 1; POF1</A><BR>
</TD>
</TR>
<TR><TD>POLA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120304">GDB:120304</A></TD><TD>Xp22.1-Xp21.3 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312040">POLYMERASE, DNA, ALPHA; POLA</A><BR>
</TD>
</TR>
<TR><TD>POU3F4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:351386">GDB:351386</A></TD><TD>Xq21.1-Xq21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304400">DEAFNESS, CONDUCTIVE, WITH STAPES FIXATION</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600420"></A><BR>
</TD>
</TR>
<TR><TD>PPMX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954669">GDB:9954669</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300055">RETARDATION WITH PSYCHOSIS, PYRAMIDAL SIGNS, AND MACROORCHIDISM</A><BR>
</TD>
</TR>
<TR><TD>PRD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:371323">GDB:371323</A></TD><TD>Xp11.3-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312550">DYSPLASIA, PRIMARY</A><BR>
</TD>
</TR>
<TR><TD>PRPS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120318">GDB:120318</A></TD><TD>Xq21-Xq27 Xq22-Xq24 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311850">PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE-I; PRPS1</A><BR>
</TD>
</TR>
<TR><TD>PRPS2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120320">GDB:120320</A></TD><TD>Xp22.3-Xp22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311860">PHOSPHORIBOSYLPYROPHOSPHATE SYNTHETASE-II; PRPS2</A><BR>
</TD>
</TR>
<TR><TD>PRS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128368">GDB:128368</A></TD><TD>Xp21-Xp11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309610">MENTAL RETARDATION, X-LINKED, SYNDROMIC-2, WITH DYSMORPHISM AND CEREBRAL</A><BR>
</TD>
</TR>
<TR><TD>RCCP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954637">GDB:9954637</A></TD><TD>Xp11.2-Xp11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=114550">CANCER, HEPATOCELLULAR</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312390">RENAL CELL CARCINOMA, PAPILLARY, X-LINKED</A><BR>
</TD>
</TR>
<TR><TD>RENBP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:133792">GDB:133792</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312420">RENIN-BINDING PROTEIN; RENBP</A><BR>
</TD>
</TR>
<TR><TD>RENS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9806348">GDB:9806348</A></TD><TD>Xp11.4-Xp11.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309500">MENTAL RETARDATION, X-LINKED, RENPENNING TYPE</A><BR>
</TD>
</TR>
<TR><TD>RP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120353">GDB:120353</A></TD><TD>Xp11.4-Xp11.23 Xp11.3-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312600">RETINITIS PIGMENTOSA-2; RP2</A><BR>
</TD>
</TR>
<TR><TD>RP6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125381">GDB:125381</A></TD><TD>Xp21.3-Xp21.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312612">PIGMENTOSA-6; RP6</A><BR>
</TD>
</TR>
<TR><TD>RPGR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118736">GDB:118736</A></TD><TD>Xp21.1-Xp21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312610">RETINITIS PIGMENTOSA-3; RP3</A><BR>
</TD>
</TR>
<TR><TD>RPS4X</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128115">GDB:128115</A></TD><TD>Xq13.1-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312760">RIBOSOMAL PROTEIN S4, X-LINKED; RPS4X</A><BR>
</TD>
</TR>
<TR><TD>RPS6KA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:365648">GDB:365648</A></TD><TD>Xp22.2-Xp22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300075">RIBOSOMAL PROTEIN S6 KINASE, 90 KD, POLYPEPTIDE 3; RPS6KA3</A><BR>
</TD>
</TR>
<TR><TD>RS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119581">GDB:119581</A></TD><TD>Xp22.2-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312700">RETINOSCHISIS; RS</A><BR>
</TD>
</TR>
<TR><TD>S11</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120361">GDB:120361</A></TD><TD>Xq26-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313460">ANTIGEN, X-LINKED, SECOND; SAX2</A><BR>
</TD>
</TR>
<TR><TD>SDYS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119590">GDB:119590</A></TD><TD>Xq26-Xq26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300037">GLYPICAN-3; GPC3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312870">SIMPSON DYSMORPHIA SYNDROME; SDYS</A><BR>
</TD>
</TR>
<TR><TD>SEDL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120372">GDB:120372</A></TD><TD>Xp22-Xp22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313400">SPONDYLOEPIPHYSEAL DYSPLASIA, LATE; SEDL</A><BR>
</TD>
</TR>
<TR><TD>SERPINA7</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120399">GDB:120399</A></TD><TD>Xq21-Xq22 Xq22-Xq22 Xq21.3-Xq22.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314200">THYROXINE-BINDING GLOBULIN OF SERUM; TBG</A><BR>
</TD>
</TR>
<TR><TD>SH2D1A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120701">GDB:120701</A></TD><TD>Xq25-Xq25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308240">IMMUNODEFICIENCY, X-LINKED PROGRESSIVE COMBINED VARIABLE</A><BR>
</TD>
</TR>
<TR><TD>SHFM2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:226635">GDB:226635</A></TD><TD>Xq26-Xq26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313350">SPLIT-HAND/SPLIT-FOOT ANOMALY, X-LINKED</A><BR>
</TD>
</TR>
<TR><TD>SLC25A5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125190">GDB:125190</A></TD><TD>Xq13-Xq26 Xq24-Xq25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300150">ADENINE NUCLEOTIDE TRANSLOCATOR 2; ANT2</A><BR>
</TD>
</TR>
<TR><TD>SMAX2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9954643">GDB:9954643</A></TD><TD>Xp-Xp </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300021">SPINAL MUSCULAR ATROPHY, X-LINKED LETHAL INFANTILE</A><BR>
</TD>
</TR>
<TR><TD>SRPX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:3811398">GDB:3811398</A></TD><TD>Xp21.1-Xp21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312610">RETINITIS PIGMENTOSA-3; RP3</A><BR>
</TD>
</TR>
<TR><TD>SRS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136337">GDB:136337</A></TD><TD>Xp21-Xp21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309583">MENTAL RETARDATION, X-LINKED, SNYDER-ROBINSON TYPE</A><BR>
</TD>
</TR>
<TR><TD>STS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120393">GDB:120393</A></TD><TD>Xp22.32-Xp22.32 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308100">ICHTHYOSIS, X-LINKED</A><BR>
</TD>
</TR>
<TR><TD>SYN1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119606">GDB:119606</A></TD><TD>Xp11.23-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313440">SYNAPSIN I; SYN1</A><BR>
</TD>
</TR>
<TR><TD>SYP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125295">GDB:125295</A></TD><TD>Xp11.23-Xp11.22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313475">SYNAPTOPHYSIN; SYP</A><BR>
</TD>
</TR>
<TR><TD>TAF1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120573">GDB:120573</A></TD><TD>Xq13-Xq26 Xq13.1-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313650">TATA BOX BINDING PROTEIN (TBP)-ASSOCIATED FACTOR 2A; TAF2A</A><BR>
</TD>
</TR>
<TR><TD>TAZ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120609">GDB:120609</A></TD><TD>Xq28-Xq28 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300069">CARDIOMYOPATHY, DILATED 3A; CMD3A</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=302060">ENDOCARDIAL FIBROELASTOSIS-2; EFE2</A><BR>
</TD>
</TR>
<TR><TD>TBX22</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10796448">GDB:10796448</A></TD><TD>Xq13.1-Xq21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=303400">CLEFT PALATE, X-LINKED; CPX</A><BR>
</TD>
</TR>
<TR><TD>TDD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119610">GDB:119610</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309150">MALE PSEUDOHERMAPHRODITISM: DEFICIENCY OF TESTICULAR 17,20-DESMOLASE;</A><BR>
</TD>
</TR>
<TR><TD>TFE3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125870">GDB:125870</A></TD><TD>Xp11.23-Xp11.22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314310">TRANSCRIPTION FACTOR FOR IMMUNOGLOBULIN HEAVY-CHAIN ENHANCER-3; TFE3</A><BR>
</TD>
</TR>
<TR><TD>THAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128158">GDB:128158</A></TD><TD>Xpter-Xqter Xq25-Xq26.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313850">THORACOABDOMINAL SYNDROME; TAS</A><BR>
</TD>
</TR>
<TR><TD>THC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125361">GDB:125361</A></TD><TD>Xp21-Xp11 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313900">THROMBOCYTOPENIA, X-LINKED; THC; XLT</A><BR>
</TD>
</TR>
<TR><TD>TIMM8A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119090">GDB:119090</A></TD><TD>Xq21-Xq22 Xq22-Xq22 Xq21.3-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304700">DEAFNESS 1, PROGRESSIVE; DFN1</A><BR>
</TD>
</TR>
<TR><TD>TIMP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119615">GDB:119615</A></TD><TD>Xp11.3-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=305370">TISSUE INHIBITOR OF METALLOPROTEINASE-1; TIMP1</A><BR>
</TD>
</TR>
<TR><TD>TKCR</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119616">GDB:119616</A></TD><TD>Xq28-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314300">TORTICOLLIS, KELOIDS, CRYPTORCHIDISM, AND RENAL DYSPLASIA; TKC</A><BR>
</TD>
</TR>
<TR><TD>TNFSF5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120632">GDB:120632</A></TD><TD>Xq26-Xq26 Xq26-Xq27.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308230">IMMUNODEFICIENCY WITH INCREASED IgM</A><BR>
</TD>
</TR>
<TR><TD>UBE1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118954">GDB:118954</A></TD><TD>Xp11.3-Xp11.23 Xp11.23-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314370">UBIQUITIN-ACTIVATING ENZYME 1; UBE1</A><BR>
</TD>
</TR>
<TR><TD>UBE2A</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131647">GDB:131647</A></TD><TD>Xq24-Xq25 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312180">UBIQUITIN-CONJUGATING ENZYME E2A; UBE2A</A><BR>
</TD>
</TR>
<TR><TD>WAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120736">GDB:120736</A></TD><TD>Xp11.3-Xp11.22 Xp11.23-Xp11.22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=301000">WISKOTT-ALDRICH SYNDROME; WAS</A><BR>
</TD>
</TR>
<TR><TD>WSN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125864">GDB:125864</A></TD><TD>Xq27-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=311510">PARKINSONISM, EARLY-ONSET, WITH MENTAL RETARDATION</A><BR>
</TD>
</TR>
<TR><TD>WTS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128373">GDB:128373</A></TD><TD>Xp11.3-Xq21 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309585">MENTAL RETARDATION, X-LINKED, SYNDROMIC-6, WITH GYNECOMASTIA AND OBESITY;</A><BR>
</TD>
</TR>
<TR><TD>WWS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120497">GDB:120497</A></TD><TD>Xq11-Xq22 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314580">WIEACKER SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>XIC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120498">GDB:120498</A></TD><TD>Xq13.2-Xq13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314670">X-INACTIVATION-SPECIFIC TRANSCRIPT; XIST</A><BR>
</TD>
</TR>
<TR><TD>XIST</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126428">GDB:126428</A></TD><TD>Xq13.2-Xq13.2 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314670">X-INACTIVATION-SPECIFIC TRANSCRIPT; XIST</A><BR>
</TD>
</TR>
<TR><TD>XK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120499">GDB:120499</A></TD><TD>Xp21.1-Xp21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314850">Xk LOCUS</A><BR>
</TD>
</TR>
<TR><TD>XM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119634">GDB:119634</A></TD><TD>Xpter-Xqter </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314900">XM SYSTEM</A><BR>
</TD>
</TR>
<TR><TD>XS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119636">GDB:119636</A></TD><TD>Xp21.2-Xq21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=309050">LUTHERAN SUPPRESSOR, X-LINKED; XS; LUXS</A><BR>
</TD>
</TR>
<TR><TD>ZFX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120502">GDB:120502</A></TD><TD>Xp22.1-Xp22.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314980">ZINC FINGER PROTEIN, X-LINKED; ZFX</A><BR>
</TD>
</TR>
<TR><TD>ZIC3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:249141">GDB:249141</A></TD><TD>Xq24-Xq27.1 Xq26-Xq26 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306955">HETEROTAXY, X-LINKED VISCERAL; HTX1</A><BR>
</TD>
</TR>
<TR><TD>ZNF261</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9785766">GDB:9785766</A></TD><TD>Xq13.1-Xq13.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300061">MENTAL RETARDATION, X-LINKED; DXS6673E</A><BR>
</TD>
</TR>
<TR><TD>ZNF41</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125865">GDB:125865</A></TD><TD>Xp11.3-Xp11.23 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314995">ZINC FINGER PROTEIN-41; ZNF41</A><BR>
</TD>
</TR>
<TR><TD>ZNF6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120508">GDB:120508</A></TD><TD>Xq21.1-Xq21.3 Xq21.1-Xq21.1 </TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=314990">ZINC FINGER PROTEIN-6; ZNF6</A><BR>
</TD>
</TR>
<TR><TD>ABAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:581658">GDB:581658</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137150">GAMMA-AMINOBUTYRATE TRANSAMINASE</A><BR>
</TD>
</TR>
<TR><TD>AEZ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128360">GDB:128360</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=201100">ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE; AEZ</A><BR>
</TD>
</TR>
<TR><TD>AFA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265277">GDB:265277</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=106250">FILIFORME ADNATUM AND CLEFT PALATE</A><BR>
</TD>
</TR>
<TR><TD>AFD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265292">GDB:265292</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=154400">DYSOSTOSIS, TREACHER COLLINS TYPE, WITH LIMB ANOMALIES</A><BR>
</TD>
</TR>
<TR><TD>ASAH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6837715">GDB:6837715</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=228000">FARBER LIPOGRANULOMATOSIS</A><BR>
</TD>
</TR>
<TR><TD>ASD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6276019">GDB:6276019</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=108800">ATRIAL SEPTAL DEFECT; ASD</A><BR>
</TD>
</TR>
<TR><TD>ASMT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:136259">GDB:136259</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300015">ACETYLSEROTONIN METHYLTRANSFERASE; ASMT</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=402500">ACETYLSEROTONIN METHYLTRANSFERASE, Y-CHROMOSOMAL; ASMTY; HIOMTY</A><BR>
</TD>
</TR>
<TR><TD>CCAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118738">GDB:118738</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212500">CATARACT, CONGENITAL OR JUVENILE</A><BR>
</TD>
</TR>
<TR><TD>CECR9</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:10796163">GDB:10796163</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115470">CAT EYE SYNDROME; CES</A><BR>
</TD>
</TR>
<TR><TD>CEPA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:581848">GDB:581848</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=209880">CONTROL, CONGENITAL FAILURE OF</A><BR>
</TD>
</TR>
<TR><TD>CLA3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128453">GDB:128453</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=117400">CEREBELLOPARENCHYMAL DISORDER I; CPD I</A><BR>
</TD>
</TR>
<TR><TD>CLN4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125229">GDB:125229</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=204300">CEROID-LIPOFUSCINOSIS, NEURONAL 4; CLN4</A><BR>
</TD>
</TR>
<TR><TD>CSF2RA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118777">GDB:118777</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=306250">COLONY STIMULATING FACTOR 2 RECEPTOR, ALPHA; CSF2RA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=425000">GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR RECEPTOR, ALPHA SUBUNIT,</A><BR>
</TD>
</TR>
<TR><TD>CTS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118779">GDB:118779</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=115430">CARPAL TUNNEL SYNDROME; CTS; CTS1</A><BR>
</TD>
</TR>
<TR><TD>DF</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132645">GDB:132645</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=134350">FACTOR D</A><BR>
</TD>
</TR>
<TR><TD>DIH1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439243">GDB:439243</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142340">DIAPHRAGMATIC</A><BR>
</TD>
</TR>
<TR><TD>DWS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128371">GDB:128371</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=220200">SYNDROME; DWS</A><BR>
</TD>
</TR>
<TR><TD>DYT2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118788">GDB:118788</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=224500">DYSTONIA MUSCULORUM DEFORMANS 2; DYT2</A><BR>
</TD>
</TR>
<TR><TD>DYT4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433751">GDB:433751</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=128101">DYSTONIA MUSCULORUM DEFORMANS 4; DYT4</A><BR>
</TD>
</TR>
<TR><TD>EBR3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118739">GDB:118739</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=226500">EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA</A><BR>
</TD>
</TR>
<TR><TD>ECT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128640">GDB:128640</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=117100">CENTRALOPATHIC EPILEPSY</A><BR>
</TD>
</TR>
<TR><TD>EEF1A1L14</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1327185">GDB:1327185</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600841">PROSTATIC CARCINOMA ONCOGENE PTI-1</A><BR>
</TD>
</TR>
<TR><TD>EYCL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:4642815">GDB:4642815</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227220">EYE COLOR-3; EYCL3</A><BR>
</TD>
</TR>
<TR><TD>FANCB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9864269">GDB:9864269</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227660">FANCONI PANCYTOPENIA, TYPE 2</A><BR>
</TD>
</TR>
<TR><TD>GCSH</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:126842">GDB:126842</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238330">HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE III; NKH3</A><BR>
</TD>
</TR>
<TR><TD>GCSL</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:132139">GDB:132139</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238331">ISOLATED NONKETOTIC, TYPE IV; NKH4</A><BR>
</TD>
</TR>
<TR><TD>GIP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119985">GDB:119985</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137240">GASTRIC INHIBITORY POLYPEPTIDE; GIP</A><BR>
</TD>
</TR>
<TR><TD>GTS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118807">GDB:118807</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=137580">GILLES DE LA TOURETTE SYNDROME; GTS</A><BR>
</TD>
</TR>
<TR><TD>HHG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118740">GDB:118740</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=238320">HYPERGONADOTROPIC HYPOGONADISM; HHG</A><BR>
</TD>
</TR>
<TR><TD>HMI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265275">GDB:265275</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146150">OF ITO; HMI</A><BR>
</TD>
</TR>
<TR><TD>HOAC</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118812">GDB:118812</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=220700">DEAFNESS, CONGENITAL, AUTOSOMAL RECESSIVE</A><BR>
</TD>
</TR>
<TR><TD>HOKPP2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:595535">GDB:595535</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600304">HYPOKALEMIC PERIODIC PARALYSIS, TYPE II; HOKPP2</A><BR>
</TD>
</TR>
<TR><TD>HRPT1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125252">GDB:125252</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145000">HYPERPARATHYROIDISM, FAMILIAL PRIMARY</A><BR>
</TD>
</TR>
<TR><TD>HSD3B3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:676973">GDB:676973</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=231100">GIANT CELL HEPATITIS, NEONATAL</A><BR>
</TD>
</TR>
<TR><TD>HTC1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265286">GDB:265286</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=145701">HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE; HTC1</A><BR>
</TD>
</TR>
<TR><TD>HV1S</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955009">GDB:9955009</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=142450">HERPES VIRUS SENSITIVITY; HV1S</A><BR>
</TD>
</TR>
<TR><TD>ICHQ</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11511156">GDB:11511156</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=242500">ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE</A><BR>
</TD>
</TR>
<TR><TD>ICR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127785">GDB:127785</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=146750">LAMELLAR, AUTOSOMAL DOMINANT FORM</A><BR>
</TD>
</TR>
<TR><TD>ICR5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127789">GDB:127789</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=242500">ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE</A><BR>
</TD>
</TR>
<TR><TD>IL3RA</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128985">GDB:128985</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=308385">INTERLEUKIN-3 RECEPTOR, ALPHA; IL3RA</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=430000">INTERLEUKIN-3 RECEPTOR, Y-CHROMOSOMAL; IL3RA</A><BR>
</TD>
</TR>
<TR><TD>KAL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:265288">GDB:265288</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147950">KALLMANN SYNDROME 2; KAL2</A><BR>
</TD>
</TR>
<TR><TD>KMS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118827">GDB:118827</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=147920">SYNDROME; KMS</A><BR>
</TD>
</TR>
<TR><TD>KRT18</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120127">GDB:120127</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=148070">KERATIN 18; KRT18</A><BR>
</TD>
</TR>
<TR><TD>KSS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9957718">GDB:9957718</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=530000">KEARNS-SAYRE SYNDROME; KSS</A><BR>
</TD>
</TR>
<TR><TD>LCAT</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:119359">GDB:119359</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=136120">FISH-EYE DISEASE; FED</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=245900">LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY</A><BR>
</TD>
</TR>
<TR><TD>LHON</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958160">GDB:9958160</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=535000">LEBER OPTIC ATROPHY</A><BR>
</TD>
</TR>
<TR><TD>LIMM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958161">GDB:9958161</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=551000">MYOPATHY, MITOCHONDRIAL, LETHAL INFANTILE; LIMM</A><BR>
</TD>
</TR>
<TR><TD>MANBB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125262">GDB:125262</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248510">MANNOSIDOSIS, BETA; MANB1</A><BR>
</TD>
</TR>
<TR><TD>MCPH2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9863035">GDB:9863035</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=251200">MICROCEPHALY; MCT</A><BR>
</TD>
</TR>
<TR><TD>MEB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:599557">GDB:599557</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=253280">DISEASE</A><BR>
</TD>
</TR>
<TR><TD>MELAS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9955855">GDB:9955855</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=540000">MELAS SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>MIC2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120184">GDB:120184</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=313470">SURFACE ANTIGEN MIC2; MIC2; CD99</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=450000">MIC2 SURFACE ANTIGEN, Y-CHROMOSOMAL; MIC2Y</A><BR>
</TD>
</TR>
<TR><TD>MPFD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439372">GDB:439372</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=255310">CONGENITAL, WITH FIBER-TYPE DISPROPORTION</A><BR>
</TD>
</TR>
<TR><TD>MS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:229116">GDB:229116</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=126200">SCLEROSIS; MS</A><BR>
</TD>
</TR>
<TR><TD>MSS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118743">GDB:118743</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=248800">MARINESCO-SJOGREN SYNDROME; MSS</A><BR>
</TD>
</TR>
<TR><TD>MTATP6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118897">GDB:118897</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516060">ATP SYNTHASE 6; MTATP6</A><BR>
</TD>
</TR>
<TR><TD>MTCO1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118900">GDB:118900</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516030">COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I; MTCO1; COI</A><BR>
</TD>
</TR>
<TR><TD>MTCO3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118902">GDB:118902</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516050">CYTOCHROME c OXIDASE III; MTCO3</A><BR>
</TD>
</TR>
<TR><TD>MTCYB</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118906">GDB:118906</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516020">COMPLEX III, CYTOCHROME b SUBUNIT</A><BR>
</TD>
</TR>
<TR><TD>MTND1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118911">GDB:118911</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516000">COMPLEX I, SUBUNIT ND1; MTND1</A><BR>
</TD>
</TR>
<TR><TD>MTND2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118912">GDB:118912</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516001">COMPLEX I, SUBUNIT ND2; MTND2</A><BR>
</TD>
</TR>
<TR><TD>MTND4</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118914">GDB:118914</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516003">COMPLEX I, SUBUNIT ND4; MTND4</A><BR>
</TD>
</TR>
<TR><TD>MTND5</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118916">GDB:118916</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516005">COMPLEX I, SUBUNIT ND5; MTND5</A><BR>
</TD>
</TR>
<TR><TD>MTND6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118917">GDB:118917</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=516006">COMPLEX I, SUBUNIT ND6; MTND6</A><BR>
</TD>
</TR>
<TR><TD>MTRNR1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118920">GDB:118920</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=561000">RIBOSOMAL RNA, MITOCHONDRIAL, 12S; MTRNR1</A><BR>
</TD>
</TR>
<TR><TD>MTRNR2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118921">GDB:118921</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=561010">RIBOSOMAL RNA, MITOCHONDRIAL, 16S; MTRNR2</A><BR>
</TD>
</TR>
<TR><TD>MTTE</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118926">GDB:118926</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590025">TRANSFER RNA, MITOCHONDRIAL, GLUTAMIC ACID; MTTE</A><BR>
</TD>
</TR>
<TR><TD>MTTG</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118933">GDB:118933</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590035">TRANSFER RNA, MITOCHONDRIAL, GLYCINE; MTTG</A><BR>
</TD>
</TR>
<TR><TD>MTTI</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118935">GDB:118935</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590045">TRANSFER RNA, MITOCHONDRIAL, ISOLEUCINE; MTTI</A><BR>
</TD>
</TR>
<TR><TD>MTTK</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118936">GDB:118936</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=545000">MERRF SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590060">TRANSFER RNA, MITOCHONDRIAL, LYSINE; MTTK</A><BR>
</TD>
</TR>
<TR><TD>MTTL1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118937">GDB:118937</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=545000">MERRF SYNDROME</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590050">TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 1; MTTL1</A><BR>
</TD>
</TR>
<TR><TD>MTTL2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118938">GDB:118938</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590055">TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 2; MTTL2</A><BR>
</TD>
</TR>
<TR><TD>MTTN</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118940">GDB:118940</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590010">TRANSFER RNA, MITOCHONDRIAL, ASPARAGINE; MTTN</A><BR>
</TD>
</TR>
<TR><TD>MTTP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118941">GDB:118941</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590075">TRANSFER RNA, MITOCHONDRIAL, PROLINE; MTTP</A><BR>
</TD>
</TR>
<TR><TD>MTTS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118944">GDB:118944</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=590080">TRANSFER RNA, MITOCHONDRIAL, SERINE, 1; MTTS1</A><BR>
</TD>
</TR>
<TR><TD>NAMSD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:681237">GDB:681237</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=310490">NEUROPATHY, MOTOR-SENSORY, TYPE II, WITH DEAFNESS AND MENTAL RETARDATION</A><BR>
</TD>
</TR>
<TR><TD>OCD1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118846">GDB:118846</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=164230">DISORDER-1; OCD1</A><BR>
</TD>
</TR>
<TR><TD>OPD2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:131394">GDB:131394</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=304120">SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>PCK2</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:137198">GDB:137198</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=261650">PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL; PCK2</A><BR>
</TD>
</TR>
<TR><TD>PCLD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:433949">GDB:433949</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=174050">POLYCYSTIC LIVER DISEASE; PLD</A><BR>
</TD>
</TR>
<TR><TD>PCOS1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:1391802">GDB:1391802</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=184700">STEIN-LEVENTHAL SYNDROME</A><BR>
</TD>
</TR>
<TR><TD>PFKM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:120277">GDB:120277</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=232800">GLYCOGEN STORAGE DISEASE VII</A><BR>
</TD>
</TR>
<TR><TD>PKD3</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:127866">GDB:127866</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600666">KIDNEY DISEASE 3, AUTOSOMAL DOMINANT; PKD3</A><BR>
</TD>
</TR>
<TR><TD>PRCA1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:342066">GDB:342066</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176807">PROSTATE CANCER; PRCA1</A><BR>
</TD>
</TR>
<TR><TD>PRO1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:128585">GDB:128585</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=176670"></A><BR>
</TD>
</TR>
<TR><TD>PROP1</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9834318">GDB:9834318</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601538">PROPHET OF PIT1, MOUSE, HOMOLOG OF; PROP1</A><BR>
</TD>
</TR>
<TR><TD>RBS</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:118862">GDB:118862</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=268300">ROBERTS SYNDROME; RBS</A><BR>
</TD>
</TR>
<TR><TD>RFXAP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9475355">GDB:9475355</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601861">REGULATORY FACTOR X-ASSOCIATED PROTEIN; RFXAP</A><BR>
</TD>
</TR>
<TR><TD>RP</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:9958158">GDB:9958158</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=180103">RETINITIS PIGMENTOSA-8</A><BR>
</TD>
</TR>
<TR><TD>SHOX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:6118451">GDB:6118451</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=312865">SHORT STATURE; SS</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=400020"></A><BR>
</TD>
</TR>
<TR><TD>SLC25A6</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:125184">GDB:125184</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=300151">ADENINE NUCLEOTIDE TRANSLOCATOR 3; ANT3</A><BR>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=403000">ADENINE NUCLEOTIDE TRANSLOCATOR 3, Y-CHROMOSOMAL; ANT3Y</A><BR>
</TD>
</TR>
<TR><TD>SPG5B</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:250333">GDB:250333</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600146">SPASTIC PARAPLEGIA-5B, AUTOSOMAL RECESSIVE; SPG5B</A><BR>
</TD>
</TR>
<TR><TD>STO</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439375">GDB:439375</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=117550">CEREBRAL GIGANTISM</A><BR>
</TD>
</TR>
<TR><TD>SUOX</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:5584405">GDB:5584405</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=272300">SULFOCYSTEINURIA</A><BR>
</TD>
</TR>
<TR><TD>THM</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:439378">GDB:439378</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=274230">FAMILIAL</A><BR>
</TD>
</TR>
<TR><TD>TTD</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:230276">GDB:230276</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=601675">TRICHOTHIODYSTROPHY; TTD</A><BR>
</TD>
</TR>
<TR><TD>WARBM1~withdrawn</TD>
<TD><A HREF="/gdb-bin/genera/genera/hgd/Gene?GDB:11518001">GDB:11518001</A></TD><TD></TD>
<TD>
<A HREF="http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600118">MICRO SYNDROME</A><BR>
</TD>
</TR>
