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genes_LOVD.html
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<!DOCTYPE HTML>
<HEAD><TITLE>FinDis - Genes</TITLE></HEAD>
<link rel="stylesheet" href="http://twitter.github.com/bootstrap/assets/css/bootstrap.css">
<style type="text/css">
body {
padding-top: 60px;
padding-bottom: 40px;
padding-left: 60px;
padding-right: 40px;
}
#heritage {
width: 92%;
margin-left: auto ;
margin-right: auto ;
}
</style>
<script src="http://ajax.googleapis.com/ajax/libs/jquery/1.7.2/jquery.min.js"></script>
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</script>
<style>
body {
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}
.disease_desc {
display: none;
}
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#loading {
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</style>
<BODY>
<div class="wpmenuspan">
<H1><img id="titlelogo" src="img/flag_lg.png"border="0"/>HVP Country Node</H1>
<span id="wpmenubloc">
<ul class="navlistop">
<li><a href="index.html" class="wpmenu"><b>Home</b> </a></li>
<li><a href="diseases.html" class="wpmenu"><b>Diseases</b></a></li>
<li><a href="genes.html" class="wpmenu"><b>Genes</b></a></li>
<li><a href="publications.html" class="wpmenu"><b>Publications</b></a></li>
<li><a href="links.html" class="wpmenu"><b>Links</b></a></li>
</ul>
</span>
<h4 class="wptitle" id="wlogotitle">Finnish Disease Database
</h4>
<!--img id="logoblock1" src="js/logoblock.png" height="" width=""/>
<img id="logoblock2" src="js/logoblock.png" height="" width=""/-->
</div>
<!--h2><IMG src="img/fin_flag_lg.png" align="middle"/>Finnish Disease Heritage</h2-->
<img src="img/blue_globe.jpeg" id="dis" height="280px" width="300px" style="position: absolute; top: -50;left: 775;">
<br/><br/><br/><br/>
<br/><br/><br/>
<h3 style="position: relative; top: -2;left: 4;"><img src="img/dna.svg" height="40" width="40" style="position: relative; top: -2;left: 2;">Genes</h3>
<comment><div id="one">
<div id="thr"></div>
<div id="two"></comment>
<div id="heritage">
<table class="table table-striped table-hover table-bordered">
<tr tableheader>
<th>Gene full name</th>
<!-- th><a href="#" class="tip" rel="tooltip" data-placement="top" style="text-align: justify; color: black;" title="Gene with Finnish variants separated from foreign. Data is fetched directly from source.">Gene/FinDis</a></th-->
<th><a href="#" class="tip" rel="tooltip" data-placement="top" style="text-align: justify; color: black;" title="Source data used to produce FinDis view (forthcoming).">
Gene/source</a></th>
<!--th><a href="#" class="tip" rel="tooltip" data-placement="top" style="text-align: justify; color: black;" title="Total mutations, Finnish + non-Finnish.">Mutations</a></th-->
<th><a href="#" class="tip" rel="tooltip" data-placement="top" style="text-align: justify; color: black;" title="View in Ensembl genome browser.">Ensembl</a></th>
</tr>
<tr class="form_listrow1">
<td>Aspartylglucosaminidase</td>
<!-- td><a href="lovd_proxy.html?gene=AGA&name=%20Aspartylglucosaminidase&ensemb=ENSG00000038002&disease=AGU&omim=208400">AGA</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/AGA" target="_blank">AGA</a></td>
<!-- td>30</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000038002">ENSG00000038002</a></td>
</tr>
<tr class="form_listrow0">
<td>Autoimmune regulator</td>
<!-- td><a href="lovd2_proxy.html?gene=AIRE&name=Autoimmune%20regulator&ensemb=ENSG00000160224&disease=APECED&omim=607358&exturl=https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CHM&extsrc=https://grenada.lumc.nl/LOVD2/mendelian_genes/home.php?select_db=AIRE&extsrctitle=Autoimmune%20regulator%20(AIRE)&curator=Roberto%20Perniola">AIRE</a></td -->
<td><a href="https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CHM" target="_blank">AIRE</a></td>
<!-- td>86</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000160224">ENSG00000160224</a></td>
</tr>
<tr class="form_listrow1">
<td>Amnionless homolog</td>
<!-- td><a href="lovd_proxy.html?gene=AMN&name=Amnionless%20homolog&ensemb=ENSG00000166126&disease=MGA1&omim=605799">AMN</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/AMN" target="_blank">AMN</a></td>
<!-- td>8</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000166126&disease=MGA1&omim=605799">ENSG00000166126</a></td>
</tr>
<tr class="form_listrow0">
<td>Aminomethyltransferase</td>
<!-- td><a href="lovd_proxy.html?gene=AMT&name=%20Aminomethyltransferase&ensemb=ENSG00000145020&disease=NKH&omim=238310">AMT</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/AMT" target="_blank">AMT</a></td>
<!-- td>23</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000145020">ENSG00000145020</a></td>
</tr>
<tr class="form_listrow1">
<td>BCS1-like</td>
<!-- td><a href="lovd_proxy.html?gene=BCS1L&name=%20BCS1-like&ensemb=ENSG00000074582&disease=GRACILE&omim=603647">BCS1L</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/BCS1L" target="_blank">BCS1L</a></td>
<!-- td>6</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000074582">ENSG00000074582</a></td>
</tr>
<tr class="form_listrow0">
<td>CHROMOSOME 10 OPEN READING FRAME 2</td>
<!-- td><a href="lovd_proxy.html?gene=C10orf2&name=FRAME%202&ensemb=ENSG00000107815&disease=IOSCA&omim=606075">C10orf2</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/C10orf2" target="_blank">C10orf2</a></td>
<!-- td>1</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000107815">ENSG00000107815</a></td>
</tr>
<tr class="form_listrow1">
<td>COILED-COIL AND C2 DOMAINS-CONTAINING PROTEIN 2A</td>
<!-- td><a href="lovd_proxy.html?gene=CC2D2A&name=%20COILED-COIL AND C2-DOMAINS-CONTAINING%20PROTEIN%202A&ensemb=ENSG00000048342&disease=MKS&omim=612013">CC2D2A</a></td-->
<td><a href="http://databases.lovd.nl/shared/genes/CC2D2A" target="_blank">CC2D2A</a></td>
<!-- td>18</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000048342">ENSG00000048342</a></td>
</tr>
<tr class="form_listrow0">
<td>CENTROSOMAL PROTEIN, 290-KD</td>
<!-- td><a href="lovd_proxy.html?gene=CEP290&name=CENTROSOMAL%20PROTEIN,%20290-KD&ensemb=ENSG00000198707&disease=MKS&omim=610142">CEP290</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/CEP290" target="_blank">CEP290</a></td>
<!-- td>15</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000198707">ENSG00000198707</a></td>
</tr>
<tr class="form_listrow1">
<td>Battenin</td>
<!-- td><a href="exturl.html?gene=CLN3&name=Battenin&ensemb=ENSG00000188603&disease=CLN3&omim=607042&exturl=http://www.ucl.ac.uk/ncl/CLN3mutationtable.htm&extsrc=http://www.ucl.ac.uk/ncl/mutation.shtml&extsrctitle=NCL%20Mutation%20and%20Patient%20Database&curator=Sara%20Mole">CLN3</a></td-->
<td><a href="http://www.ucl.ac.uk/ncl/CLN3mutationtable.htm" target="_blank">CLN3</a></td>
<!-- td>26</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000188603">ENSG00000188603</a></td>
</tr>
<tr class="form_listrow0">
<td>Ceroid-lipofuscinosis neuronal protein 5 Precursor</td>
<!-- td><a href="exturl.html?gene=CLN5&name=Ceroid-lipofuscinosis%20neuronal%20protein%205%20Precursor&ensemb=ENSG00000102805&disease=CLN5&omim=608102&exturl=http://www.ucl.ac.uk/ncl/CLN5mutationtable.htm&extsrc=http://www.ucl.ac.uk/ncl/mutation.shtml&extsrctitle=NCL%20Mutation%20and%20Patient%20Database&curator=Sara%20Mole">CLN5</a></td -->
<td><a href="http://www.ucl.ac.uk/ncl/CLN5mutationtable.htm" target="_blank">CLN5</a></td>
<!-- td>23</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000102805">ENSG00000102805</a></td>
</tr>
<tr class="form_listrow1">
<td>Ceroid-lipofuscinosis neuronal 8 protein</td>
<!-- td><a href="exturl.html?gene=CLN8&name=Ceroid-lipofuscinosis%20neuronal%208%20protein&ensemb=ENSG00000182372&disease=EPMR&omim=607837&exturl=http://www.ucl.ac.uk/ncl/CLN8mutationtable.htm&extsrc=http://www.ucl.ac.uk/ncl/mutation.shtml&extsrctitle=NCL%20Mutation%20and%20Patient%20Database&curator=Sara%20Mole">CLN8</a></td-->
<td><a href="http://www.ucl.ac.uk/ncl/CLN8mutationtable.htm" target="_blank">CLN8</a></td>
<!-- td>1</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000182372">ENSG00000182372</a></td>
</tr>
<tr class="form_listrow0">
<td>Cohen syndrome protein 1</td>
<!-- td><a href="lovd_proxy.html?gene=VPS13B&name=Cohen%20syndrome%20protein%201&ensemb=ENSG00000132549&disease=COH1&omim=607817">COH1</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/COH1" target="_blank">COH1</a></td>
<!-- td>111</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000132549">ENSG00000132549</a></td>
</tr>
<tr class="form_listrow1">
<td>Cystatin B</td>
<!-- td><a href="lovd_proxy.html?gene=CSTB&name=Cystatin%20B&ensemb=ENSG00000160213&disease=EPM1&omim=601145">CSTB</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/CSTB" target="_blank">CSTB</a></td>
<!-- td>10</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000160213">ENSG00000160213</a></td>
</tr>
<tr class="form_listrow0">
<td>Cubilin</td>
<!-- td><a href="lovd_proxy.html?gene=CUBN&name=%20Cubilin&ensemb=ENSG00000107611&disease=MGA1&omim=602997">CUBN</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/CUBN" target="_blank">CUBN</a></td>
<!-- td>8</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000107611">ENSG00000107611</a></td>
</tr>
<tr class="form_listrow1">
<td>DNAX-activation protein 12</td>
<!-- td><a href="lovd_proxy.html?gene=TYROBP&name=DNAX-activation%20protein%2012&ensemb=ENSG00000011600&disease=PLOSL&omim=604142">DAP12</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/DAP12" target="_blank">DAP12</a></td>
<!-- td>8</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000011600">ENSG00000011600</a></td>
</tr>
<tr class="form_listrow0">
<td>Follicle stimulating hormone receptor</td>
<!-- td><a href="lovd_proxy.html?gene=FSHR&name=Follicle%20stimulating%20hormone%20receptor&ensemb=ENSG00000170820&disease=ODG1&omim=136435">FSHR</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/FSHR" target="_blank">FSHR</a></td>
<!-- td>10</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000170820">ENSG00000170820</a></td>
</tr>
<tr class="form_listrow1">
<td>Glycine cleavage system H protein</td>
<!-- td><a href="lovd_proxy.html?gene=GCSH&name=Glycine%20cleavage%20system%20H%20protein&ensemb=ENSG00000140905&disease=GCE&omim=238330">GCSH</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/GCSH" target="_blank">GCSH</a></td>
<!-- td>4</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000140905">ENSG00000140905</a></td>
</tr>
<tr class="form_listrow0">
<td>Glycine decarboxylase</td>
<!-- td><a href="lovd_proxy.html?gene=GLDC&name=Glycine%20decarboxylase&ensemb=ENSG00000049496&disease=GCE&omim=238300">GLDC</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/GLDC" target="_blank">GLDC</a></td>
<!-- td>112</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000049496">ENSG00000049496</a></td>
</tr>
<tr class="form_listrow1">
<td>GLE1-like protein - assoc. w. LAAHD</td>
<!-- td><a href="lovd_proxy.html?gene=GLE1&name=GLE1-like%20protein&ensemb=ENSG00000119392&disease=LAAHD&omim=603371">GLE1</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/GLE1" target="_blank">GLE1</a></td>
<!-- td>4</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000119392">ENSG00000119392</a></td>
</tr>
<tr class="form_listrow1">
<td>GLE1-like protein - assoc. w. LCCS1</td>
<!-- td><a href="lovd_proxy.html?gene=GLE1&name=GLE1-like%20protein&ensemb=ENSG00000119392&disease=LCCS1&omim=603371">GLE1</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/GLE1" target="_blank">GLE1</a></td>
<!-- td>4</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000119392">ENSG00000119392</a></td>
</tr>
<tr class="form_listrow0">
<td>Gelsolin</td>
<!-- td><a href="lovd_proxy.html?gene=GSN&name=%20Gelsolin&ensemb=ENSG00000148180&disease=FAF&omim=137350">GSN</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/GSN" target="_blank">GSN</a></td>
<!-- td>2</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000148180">ENSG00000148180</a></td>
</tr>
<tr class="form_listrow1">
<td>Hydrolethalus syndrome protein 1</td>
<!-- td><a href="lovd_proxy.html?gene=HYLS1&name=Hydrolethalus%20syndrome%20protein%201&ensemb=ENSG00000198331&disease=HLS&omim=610693">HYLS1</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/HYLS1" target="_blank">HYLS1</a></td>
<!-- td>1</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000198331">ENSG00000198331</a></td>
</tr>
<tr class="form_listrow0">
<td>Keratocan</td>
<!-- td><a href="lovd_proxy.html?gene=KERA&name=%20Keratocan&ensemb=ENSG00000139330&disease=CNA2&omim=603288">KERA</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/KERA" target="_blank">KERA</a></td>
<!-- td>6</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000139330">ENSG00000139330</a></td>
</tr>
<tr class="form_listrow1">
<td>Lactase</td>
<!-- td><a href="lovd_proxy.html?gene=LCT&name=%20Lactase&ensemb=ENSG00000115850&disease=Lactase%20deficiency,congenital&omim=603202">LCT</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/LCT" target="_blank">LCT</a></td>
<!-- td>9</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000115850">ENSG00000115850</a></td>
</tr>
<tr class="form_listrow0">
<td>Meckel syndrome type 1 protein</td>
<!-- td><a href="lovd_proxy.html?gene=MKS1&name=Meckel%20syndrome%20type%201%20protein&ensemb=ENSG00000011143&disease=MKS1&omim=609883">MKS1</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/MKS1" target="_blank">MKS1</a></td>
<!-- td>18</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000011143">ENSG00000011143</a></td>
</tr>
<tr class="form_listrow1">
<td>Nephrin</td>
<!-- td><a href="lovd_proxy.html?gene=NPHS1&name=%20Nephrin&ensemb=ENSG00000161270&disease=CNF&omim=602716">NPHS1</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/NPHS1" target="_blank">NPHS1</a></td>
<!-- td>119</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000161270">ENSG00000161270</a></td>
</tr>
<tr class="form_listrow0">
<td>Ornithine aminotransferase</td>
<!-- td><a href="lovd2_eye_proxy.html?gene=OAT&name=Ornithine%20aminotransferase&ensemb=ENSG00000065154&disease=GA&omim=258870&exturl=http://grenada.lumc.nl/LOVD2/eye/variants_overview_origin.php?order=&hide_col=&show_col=&genes%5B%5D=OAT&search_Patient%2FOrigin%2FGeographic%5B%5D=Finland&search_Patient%2FOrigin%2FEthnic=&extsrc=http://grenada.lumc.nl/LOVD2/eye/home.php?select_db=OAT&extsrctitle=Eye%20diseases%20-%20LOVD&curator=Eva%20Trevisson%20and%20Mara%20Doimo">OAT</a></td -->
<td><a href="http://grenada.lumc.nl/LOVD2/eye/home.php?select_db=OAT" target="_blank">OAT</a></td>
<!-- td>55</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000065154">ENSG00000065154</a></td>
</tr>
<tr class="form_listrow1">
<td>Protein O-mannose beta-1,2-N-acetylglucosaminyltransferase</td>
<!-- td><a href="lovd_proxy.html?gene=POMGNT1&name=Protein%20O-mannose%20beta-1,2-N-acetylglucosaminyltransferase&ensemb=ENSG00000085998&disease=MDDGA3&omim=606822">POMGNT1</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/POMGNT1" target="_blank">POMGNT1</a></td>
<!-- td>41</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000085998">ENSG00000085998</a></td>
</tr>
<tr class="form_listrow0">
<td>Palmitoyl protein thioesterase 1</td>
<!--td><a href="exturl.html?gene=PPT1&name=Palmitoyl%20protein%20thioesterase%201&ensemb=ENSG00000131238&disease=CLN1&omim=600722&exturl=http://www.ucl.ac.uk/ncl/CLN1mutationtable.htm&extsrc=http://www.ucl.ac.uk/ncl/mutation.shtml&extsrctitle=NCL%20Mutation%20and%20Patient%20Database&curator=Sara%20Mole">PPT1</a></td-->
<td><a href="http://www.ucl.ac.uk/ncl/CLN1mutationtable.htm" target="_blank">PPT1</a></td>
<!-- td>49</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000131238">ENSG00000131238</a></td>
</tr>
<tr class="form_listrow1">
<td>RecQ protein-like 4</td>
<!-- td><a href="lovd_proxy.html?gene=RECQL4&name=RecQ%20protein-like%204&ensemb=ENSG00000160957&disease=RAPADILINO&omim=603780">RECQL4</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/RECQL4" target="_blank">RECQL4</a></td>
<!-- td>11</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000160957">ENSG00000160957</a></td>
</tr>
<tr class="form_listrow0">
<td>Rab escort protein 1</td>
<!-- td><a href="lovd2_usher_proxy.html?gene=CHM&name=Rab%20escort%20protein%201&ensemb=ENSG00000188419&disease=CHM&omim=300390&exturl=https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CHM&extsrc=https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CHM&extsrctitle=Retinal%20and%20hearing%20impairment%20genetic%20mutation%20database&curator=David%20Baux">REP1</a></td -->
<td><a href="https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CHM" target="_blank">REP1</a></td>
<!-- td>132</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000188419">ENSG00000188419</a></td>
</tr>
<tr class="form_listrow1">
<td>Ribonuclease mitochondrial RNA processing</td>
<!-- td><a href="lovd_proxy.html?gene=RMRP&name=Ribonuclease%20mitochondrial%20RNA%20processing&ensemb=ENSG00000199916&disease=CHH&omim=157660">RMRP</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/RMRP" target="_blank">RMRP</a></td>
<!-- td>96</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000199916">ENSG00000199916</a></td>
</tr>
<tr class="form_listrow0">
<td>RPGR-interacting protein 1-like protein</td>
<!-- td><a href="lovd_proxy.html?gene=RPGRIP1L&name=RPGR-interacting%20protein%201-like%20protein&ensemb=ENSG00000103494&disease=MKS1&omim=610937">RPGRIP1L</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/RPGRIP1L" target="_blank">RPGRIP1L</a></td>
<!-- td>3</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000103494">ENSG00000103494</a></td>
</tr>
<tr class="form_listrow1">
<td>Retinoschisis 1 gene</td>
<!-- td><a href="lovd2_eye_proxy.html?gene=RS1&name=Retinoschisi%201%20gene&ensemb=ENSG00000102104&disease=RS1&omim=312700&exturl=http://grenada.lumc.nl/LOVD2/eye/variants_overview_origin.php?order=%26hide_col=%26show_col=%26genes%5B%5D=RS1%26search_Patient%2FOrigin%2FGeographic%5B%5D=Finland&search_Patient%2FOrigin%2FEthnic=&extsrc=http://grenada.lumc.nl/LOVD2/eye/home.php?select_db=RS1&extsrctitle=Eye%20diseases%20-%20LOVD&curator=Johan%20den%20Dunnen">RS1</a></td -->
<td><a href="http://grenada.lumc.nl/LOVD2/eye/home.php?select_db=RS1" target="_blank">RS1</a></td>
<!-- td>176</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000102104">ENSG00000102104</a></td>
</tr>
<tr class="form_listrow0">
<td>Solute carrier family 17, member 5</td>
<!-- td><a href="lovd_proxy.html?gene=SLC17A5&name=Solute%20carrier%20family%2017,%20member%205&ensemb=ENSG00000119899&disease=SD&omim=604322">SLC17A5</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/SLC17A5" target="_blank">SLC17A5</a></td>
<!-- td>14</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000119899">ENSG00000119899</a></td>
</tr>
<tr class="form_listrow1">
<td>Solute carrier family 26, member 2</td>
<!-- td><a href="lovd_proxy.html?gene=SLC26A2&name=Solute%20carrier%20family%2026,%20member%202&ensemb=ENSG00000155850&disease=DTD&omim=606718">SLC26A2</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/SLC26A2" target="_blank">SLC26A2</a></td>
<!-- td>29</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000155850">ENSG00000155850</a></td>
</tr>
<tr class="form_listrow0">
<td>Solute carrier family 26, member 3</td>
<!-- td><a href="lovd_proxy.html?gene=SLC26A3&name=Solute%20carrier%20family%2026,%20member%203&ensemb=ENSG00000091138&disease=CLD&omim=126650">SLC26A3</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/SLC26A3" target="_blank">SLC26A3</a></td>
<!-- td>31</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000091138">ENSG00000091138</a></td>
</tr>
<tr class="form_listrow1">
<td>Soluble carrier family 7, member 2</td>
<!-- td><a href="lovd_proxy.html?gene=SLC7A7&name=Soluble%20carrier%20family%207,%20member%202&ensemb=ENSG00000155465&disease=LPI&omim=603593">SLC7A7</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/SLC7A7" target="_blank">SLC7A7</a></td>
<!-- td>54</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000155465">ENSG00000155465</a></td>
</tr>
<tr class="form_listrow0">
<td>Transmembrane protein 216</td>
<!-- td><a href="lovd_proxy.html?gene=TMEM216&name=Transmembrane%20protein%20216&ensemb=ENSG00000187049&disease=MKS1&omim=000000">TMEM216</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/TMEM216" target="_blank">TMEM216</a></td>
<!-- td>3</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g="></a></td>
</tr>
<tr class="form_listrow1">
<td>Transmembrane protein 67</td>
<!-- td><a href="lovd_proxy.html?gene=TMEM67&name=Transmembrane%20protein%2067&ensemb=ENSG00000164953&disease=MKS&omim=609884">TMEM67</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/TMEM67" target="_blank">TMEM67</a></td>
<!-- td>36</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000164953">ENSG00000164953</a></td>
</tr>
<tr class="form_listrow0">
<td>Triggering receptor expressed on myeloid cells 2</td>
<!-- td><a href="lovd_proxy.html?gene=TREM2&name=Triggering%20receptor%20expressed%20on%20myeloid%20cells%202&ensemb=ENSG00000095970&disease=PLOSL&omim=605086">TREM2</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/TREM2" target="_blank">TREM2</a></td>
<!-- td>11</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000095970">ENSG00000095970</a></td>
</tr>
<tr class="form_listrow1">
<td>Tripartite motif-containing 37</td>
<!-- td><a href="lovd_proxy.html?gene=TRIM37&name=Tripartite%20motif-containing%2037&ensemb=ENSG00000108395&disease=MUL&omim=605073">TRIM37</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/TRIM37" target="_blank">TRIM37</a></td>
<!-- td>14</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000108395">ENSG00000108395</a></td>
</tr>
<tr class="form_listrow0">
<td>Titin</td>
<!-- td><a href="lovd_proxy.html?gene=TTN&name=Titin&ensemb=ENSG00000155657&disease=TMD&omim=188840">TTN</a></td -->
<td><a href="http://databases.lovd.nl/shared/genes/TTN" target="_blank">TTN</a></td>
<!-- td>7</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000155657">ENSG00000155657</a></td>
</tr>
<tr class="form_listrow1">
<td>Usher syndrome type III gene</td>
<!-- td><a href="lovd2_usher_proxy.html?gene=CLRN1&name=Usher%20syndrome%20Type%20IIIA&ensemb=ENSG00000163646&disease=USH3A&omim=276902&exturl=https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CLRN1&extsrc=https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CLRN1&extsrctitle=Retinal%20and%20hearing%20impairment%20genetic%20mutation%20database&curator=David%20Baux">USH3A</a></td -->
<td><a href="https://grenada.lumc.nl/LOVD2/Usher_montpellier/home.php?select_db=CLRN1" target="_blank">USH3A</a></td>
<!-- td>11</td -->
<td><a href="http://www.ensembl.org/Homo_sapiens/Location/View?g=ENSG00000163646">ENSG00000163646</a></td>
</tr>
</table>
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