nih-gov/www.ncbi.nlm.nih.gov/omim/610149

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Entry
- #610149 - MACULAR DEGENERATION, AGE-RELATED, 7; ARMD7
- OMIM
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<span class="h4">#610149</span>
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<a href="#phenotypeMap"><strong>Phenotype-Gene Relationships</strong></a>
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<a href="/phenotypicSeries/PS603075"> <strong>Phenotypic Series</strong> </a>
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<a href="#mapping">Mapping</a>
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<a href="#molecularGenetics">Molecular Genetics</a>
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<a href="#animalModel">Animal Model</a>
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<a href="#references"><strong>References</strong></a>
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<a href="#contributors"><strong>Contributors</strong></a>
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<a href="#creationDate"><strong>Creation Date</strong></a>
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<div><a href="https://clinicaltrials.gov/search?cond=(MACULAR DEGENERATION, AGE-RELATED) OR (HTRA1)" class="mim-tip-hint" title="Clinical Trials" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></div>
<div><a href="https://www.diseaseinfosearch.org/x/7657" class="mim-tip-hint" title="Network of disease-specific advocacy organizations, universities, private companies, government agencies, and public policy organizations." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Genetic Alliance', 'domain': 'diseaseinfosearch.org'})">Genetic Alliance</a></div>
<div><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=610149[mim]" class="mim-tip-hint" title="Genetic Testing Registry." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GTR', 'domain': 'ncbi.nlm.nih.gov'})">GTR</a></div>
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</div>
<div class="panel panel-default" style="margin-top: 0px; border-radius: 0px">
<div class="panel-heading mim-panel-heading" role="tab" id="mimAnimalModels">
<span class="panel-title">
<span class="small">
<a href="#mimAnimalModelsLinksFold" id="mimAnimalModelsLinksToggle" class="collapsed mimSingletonTriangleToggle" role="button" data-toggle="collapse" data-parent="#mimExternalLinksAccordion">
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<div id="mimAnimalModelsLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5; display: table-cell;">&#9658;</div>
&nbsp;
<div style="display: table-cell;">Animal Models</div>
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</span>
</div>
<div id="mimAnimalModelsLinksFold" class="panel-collapse collapse mimLinksFold" role="tabpanel">
<div class="panel-body small mim-panel-body">
<div><a href="https://www.alliancegenome.org/disease/DOID:0110019" class="mim-tip-hint" title="Search Across Species; explore model organism and human comparative genomics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Alliance Genome', 'domain': 'alliancegenome.org'})">Alliance Genome</a></div>
<div><a href="http://www.informatics.jax.org/disease/610149" class="mim-tip-hint" title="Phenotypes, alleles, and disease models from Mouse Genome Informatics." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Phenotype', 'domain': 'informatics.jax.org'})">MGI Mouse Phenotype</a></div>
<div><a href="https://omia.org/OMIA002142/" class="mim-tip-hint" title="Online Mendelian Inheritance in Animals (OMIA) is a database of genes, inherited disorders and traits in 191 animal species (other than human and mouse.)" target="_blank">OMIA</a></div>
</div>
</div>
</div>
</div>
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</div>
<span>
<span class="mim-tip-bottom" qtip_title="<strong>Looking for this gene or this phenotype in other resources?</strong>" qtip_text="Select a related resource from the dropdown menu and click for a targeted link to information directly relevant.">
&nbsp;
</span>
</span>
</div>
<div class="col-lg-8 col-lg-pull-2 col-md-8 col-md-pull-2 col-sm-8 col-sm-pull-2 col-xs-12">
<div>
<a id="title" class="mim-anchor"></a>
<div>
<a id="number" class="mim-anchor"></a>
<div class="text-right">
<a href="#" class="mim-tip-icd" qtip_title="<strong>ICD+</strong>" qtip_text="
<strong>DO:</strong> 0110019<br />
">ICD+</a>
</div>
<div>
<span class="h3">
<span class="mim-font mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
610149
</span>
</span>
</div>
</div>
<div>
<a id="preferredTitle" class="mim-anchor"></a>
<h3>
<span class="mim-font">
MACULAR DEGENERATION, AGE-RELATED, 7; ARMD7
</span>
</h3>
</div>
<div>
<br />
</div>
<div>
<a id="includedTitles" class="mim-anchor"></a>
<div>
<p>
<span class="mim-font">
Other entities represented in this entry:
</span>
</p>
</div>
<div>
<span class="h3 mim-font">
MACULAR DEGENERATION, AGE-RELATED, NEOVASCULAR TYPE, SUSCEPTIBILITY TO, INCLUDED
</span>
</div>
<div>
<span class="h4 mim-font">
MACULAR DEGENERATION, AGE-RELATED, WET TYPE, SUSCEPTIBILITY TO, INCLUDED
</span>
</div>
</div>
<div>
<br />
</div>
</div>
<div>
<a id="phenotypeMap" class="mim-anchor"></a>
<h4>
<span class="mim-font">
<strong>Phenotype-Gene Relationships</strong>
</span>
</h4>
<div>
<table class="table table-bordered table-condensed table-hover small mim-table-padding">
<thead>
<tr class="active">
<th>
Location
</th>
<th>
Phenotype
</th>
<th>
Phenotype <br /> MIM number
</th>
<th>
Inheritance
</th>
<th>
Phenotype <br /> mapping key
</th>
<th>
Gene/Locus
</th>
<th>
Gene/Locus <br /> MIM number
</th>
</tr>
</thead>
<tbody>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/624?start=-3&limit=10&highlight=624">
10q26.13
</a>
</span>
</td>
<td>
<span class="mim-font">
{Macular degeneration, age-related, 7}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610149"> 610149 </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
HTRA1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602194"> 602194 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/624?start=-3&limit=10&highlight=624">
10q26.13
</a>
</span>
</td>
<td>
<span class="mim-font">
{Macular degeneration, age-related, neovascular type}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610149"> 610149 </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
HTRA1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602194"> 602194 </a>
</span>
</td>
</tr>
</tbody>
</table>
</div>
</div>
<div>
<div class="btn-group">
<a href="/phenotypicSeries/PS603075" class="btn btn-info" role="button"> Phenotypic Series </a>
<button type="button" id="mimPhenotypicSeriesToggle" class="btn btn-info dropdown-toggle mimSingletonFoldToggle" data-toggle="collapse" href="#mimPhenotypicSeriesFold" onclick="ga('send', 'event', 'Unfurl', 'PhenotypicSeries', 'omim.org')">
<span class="caret"></span>
<span class="sr-only">Toggle Dropdown</span>
</button>
</div>
&nbsp;
<div class="btn-group">
<button type="button" class="btn btn-success dropdown-toggle" data-toggle="dropdown" aria-haspopup="true" aria-expanded="false">
PheneGene Graphics <span class="caret"></span>
</button>
<ul class="dropdown-menu" style="width: 17em;">
<li><a href="/graph/linear/610149" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Linear'})"> Linear </a></li>
<li><a href="/graph/radial/610149" target="_blank" onclick="gtag('event', 'mim_graph', {'destination': 'Radial'})"> Radial </a></li>
</ul>
</div>
<span class="glyphicon glyphicon-question-sign mim-tip-hint" title="OMIM PheneGene graphics depict relationships between phenotypes, groups of related phenotypes (Phenotypic Series), and genes.<br /><a href='/static/omim/pdf/OMIM_Graphics.pdf' target='_blank'>A quick reference overview and guide (PDF)</a>"></span>
<div>
<p />
</div>
<div id="mimPhenotypicSeriesFold" class="well well-sm collapse mimSingletonToggleFold">
<div class="small">
<div class="row">
<div class="col-lg-12 col-md-12 col-sm-12 col-xs-12">
<h5>
Macular degeneration, age-related
- <a href="/phenotypicSeries/PS603075">PS603075</a>
- 20 Entries
</h5>
</div>
</div>
<div class="row" style="margin-left: 0.125em; margin-right: 0.125em;">
<table class="table table-bordered table-condensed table-hover mim-table-padding">
<thead>
<tr>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Location</strong>
</th>
<th class="col-lg-5 col-md-5 col-sm-5 col-xs-6 text-nowrap">
<strong>Phenotype</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Inheritance</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />mapping key</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Phenotype<br />MIM number</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus</strong>
</th>
<th class="col-lg-1 col-md-1 col-sm-1 col-xs-1 text-nowrap">
<strong>Gene/Locus<br />MIM number</strong>
</th>
</tr>
</thead>
<tbody>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/814?start=-3&limit=10&highlight=814"> 1p22.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/153800"> {Macular degeneration, age-related, 2} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/153800"> 153800 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601691"> ABCA4 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601691"> 601691 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1502?start=-3&limit=10&highlight=1502"> 1q25.3-q31.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> {Macular degeneration, age-related, 1} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> 603075 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608548"> HMCN1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/608548"> 608548 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1528?start=-3&limit=10&highlight=1528"> 1q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610698"> {Macular degeneration, age-related, 4} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610698"> 610698 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134370"> CFH </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134370"> 134370 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1529?start=-3&limit=10&highlight=1529"> 1q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> {Macular degeneration, age-related, reduced risk of} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> 603075 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605336"> CFHR3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605336"> 605336 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/1/1530?start=-3&limit=10&highlight=1530"> 1q31.3 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> {Macular degeneration, age-related, reduced risk of} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603075"> 603075 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134371"> CFHR1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/134371"> 134371 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/189?start=-3&limit=10&highlight=189"> 3p22.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613784"> {Macular degeneration, age-related, 12} </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613784"> 613784 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601470"> CX3CR1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601470"> 601470 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/4/482?start=-3&limit=10&highlight=482"> 4q25 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615439"> {Macular degeneration, age-related, 13, susceptibility to} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615439"> 615439 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/217030"> CFI </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/217030"> 217030 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/126?start=-3&limit=10&highlight=126"> 5p13.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615591"> {Macular degeneration, age-related, 15, susceptibility to} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615591"> 615591 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120940"> C9 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/120940"> 120940 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/342?start=-3&limit=10&highlight=342"> 6p21.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615489"> {Macular degeneration, age-related, 14, reduced risk of} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Digenic dominant">DD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615489"> 615489 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613927"> C2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613927"> 613927 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/343?start=-3&limit=10&highlight=343"> 6p21.33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615489"> {Macular degeneration, age-related, 14, reduced risk of} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Digenic dominant">DD</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/615489"> 615489 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/138470"> CFB </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/138470"> 138470 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/9/416?start=-3&limit=10&highlight=416"> 9q32-q33 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611488"> Macular degeneration, age-related, 10 </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="2 - The disorder was placed on the map by statistical methods"> 2 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611488"> 611488 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611488"> ARMD10 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611488"> 611488 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/190?start=-3&limit=10&highlight=190"> 10q11.23 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613761"> {Macular degeneration, age-related, susceptibility to, 5} </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613761"> 613761 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609413"> ERCC6 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/609413"> 609413 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/623?start=-3&limit=10&highlight=623"> 10q26.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613778"> {Macular degeneration, age-related, 8} </a>
</span>
</td>
<td>
<span class="mim-font">
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613778"> 613778 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611313"> LOC387715 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/611313"> 611313 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/10/624?start=-3&limit=10&highlight=624"> 10q26.13 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610149"> {Macular degeneration, age-related, 7} </a>
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<span class="mim-font">
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/610149"> 610149 </a>
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<a href="/entry/602194"> HTRA1 </a>
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<a href="/entry/602194"> 602194 </a>
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<a href="/geneMap/10/624?start=-3&limit=10&highlight=624"> 10q26.13 </a>
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<span class="mim-font">
<a href="/entry/610149"> {Macular degeneration, age-related, neovascular type} </a>
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<span class="mim-font">
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/610149"> 610149 </a>
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<span class="mim-font">
<a href="/entry/602194"> HTRA1 </a>
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<span class="mim-font">
<a href="/entry/602194"> 602194 </a>
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<span class="mim-font">
<a href="/geneMap/14/464?start=-3&limit=10&highlight=464"> 14q32.12 </a>
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<span class="mim-font">
<a href="/entry/608895"> Macular degeneration, age-related, 3 </a>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/608895"> 608895 </a>
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<span class="mim-font">
<a href="/entry/604580"> FBLN5 </a>
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<span class="mim-font">
<a href="/entry/604580"> 604580 </a>
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<span class="mim-font">
<a href="/geneMap/19/117?start=-3&limit=10&highlight=117"> 19p13.3 </a>
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<span class="mim-font">
<a href="/entry/613757"> ?Macular degeneration, age-related, 6 </a>
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<span class="mim-font">
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/613757"> 613757 </a>
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<span class="mim-font">
<a href="/entry/610362"> RAX2 </a>
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<span class="mim-font">
<a href="/entry/610362"> 610362 </a>
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<span class="mim-font">
<a href="/geneMap/19/189?start=-3&limit=10&highlight=189"> 19p13.3 </a>
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<span class="mim-font">
<a href="/entry/611378"> {Macular degeneration, age-related, 9} </a>
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<span class="mim-font">
</span>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/611378"> 611378 </a>
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<span class="mim-font">
<a href="/entry/120700"> C3 </a>
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<span class="mim-font">
<a href="/entry/120700"> 120700 </a>
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<span class="mim-font">
<a href="/geneMap/19/803?start=-3&limit=10&highlight=803"> 19q13.32 </a>
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<span class="mim-font">
<a href="/entry/603075"> {?Macular degeneration, age-related} </a>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/603075"> 603075 </a>
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<span class="mim-font">
<a href="/entry/107741"> APOE </a>
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<span class="mim-font">
<a href="/entry/107741"> 107741 </a>
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</tr>
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<span class="mim-font">
<a href="/geneMap/20/154?start=-3&limit=10&highlight=154"> 20p11.21 </a>
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</td>
<td>
<span class="mim-font">
<a href="/entry/611953"> {Macular degeneration, age-related, 11} </a>
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<span class="mim-font">
</span>
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<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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<span class="mim-font">
<a href="/entry/611953"> 611953 </a>
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<span class="mim-font">
<a href="/entry/604312"> CST3 </a>
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<span class="mim-font">
<a href="/entry/604312"> 604312 </a>
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</table>
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<a href="#mimPhenotypicSeriesFold" data-toggle="collapse">&#9650;&nbsp;Close</a>
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<strong>TEXT</strong>
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<p>A number sign (#) is used with this entry because of evidence that susceptibility to age-related macular degeneration-7 (ARMD7) is conferred by variation in the HTRA1 gene (<a href="/entry/602194">602194</a>) on chromosome 10q26.</p><p>See also ARMD8 (<a href="/entry/613778">613778</a>) for a discussion of the relationship of another gene in the 10q26 region, ARMS2 (<a href="/entry/611313">611313</a>; also known as LOC387715), and susceptibility to ARMD.</p><p>For a phenotypic description and a discussion of genetic heterogeneity of age-related macular degeneration, see <a href="/entry/603075">603075</a>.</p>
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<a id="mapping" class="mim-anchor"></a>
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<strong>Mapping</strong>
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<p>Several studies had suggested specific ARMD susceptibility genes in the 10q26 region (e.g., <a href="#8" class="mim-tip-reference" title="Majewski, J., Schultz, D. W., Weleber, R. G., Schain, M. B., Edwards, A. O., Matise, T. C., Acott, T. S., Ott, J., Klein, M. L. &lt;strong&gt;Age-related macular degeneration--a genome scan in extended families.&lt;/strong&gt; Am. J. Hum. Genet. 73: 540-550, 2003.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/12900797/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;12900797&lt;/a&gt;, &lt;a href=&quot;https://www.ncbi.nlm.nih.gov/pmc/?term=12900797[PMID]&amp;report=imagesdocsum&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed Image&#x27;, &#x27;domain&#x27;: &#x27;ncbi.nlm.nih.gov&#x27;})&quot;&gt;images&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1086/377701&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="12900797">Majewski et al. (2003)</a>, <a href="#11" class="mim-tip-reference" title="Seddon, J. M., Santangelo, S. L., Book, K., Chong, S., Cote, J. &lt;strong&gt;A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions.&lt;/strong&gt; Am. J. Hum. Genet. 73: 780-790, 2003.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/12945014/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;12945014&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1086/378505&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="12945014">Seddon et al. (2003)</a>, <a href="#7" class="mim-tip-reference" title="Kenealy, S. J., Schmidt, S., Agarwal, A., Postel, E. A., De La Paz, M. A., Pericak-Vance, M. A., Haines, J. L. &lt;strong&gt;Linkage analysis for age-related macular degeneration supports a gene on chromosome 10q26.&lt;/strong&gt; Molec. Vis. 10: 57-61, 2004.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/14758336/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;14758336&lt;/a&gt;]" pmid="14758336">Kenealy et al. (2004)</a>, <a href="#3" class="mim-tip-reference" title="Fisher, S. A., Abecasis, G. R., Yashar, B. M., Zareparsi, S., Swaroop, A., Iyengar, S. K., Klein, B. E. K., Klein, R., Lee, K. E., Majewski, J., Schultz, D. W., Klein, M. L., and 13 others. &lt;strong&gt;Meta-analysis of genome scans of age-related macular degeneration.&lt;/strong&gt; Hum. Molec. Genet. 14: 2257-2264, 2005.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/15987700/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;15987700&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1093/hmg/ddi230&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="15987700">Fisher et al. (2005)</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?term=15987700+12900797+14758336+12945014" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<div>
<a id="molecularGenetics" class="mim-anchor"></a>
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<strong>Molecular Genetics</strong>
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<p>The neovascular, or wet, type of ARMD is more prevalent among Asians than among Caucasians, and the soft indistinct drusen characteristic of dry, or nonneovascular, ARMD are rarely seen in Asian individuals. To identify novel genetic variants that predispose individuals to the wet ARMD phenotype, <a href="#2" class="mim-tip-reference" title="DeWan, A., Liu, M., Hartman, S., Zhang, S. S.-M., Liu, D. T. L., Zhao, C., Tam, P. O. S., Chan, W. M., Lam, D. S. C., Snyder, M., Barnstable, C., Pang, C. P., Hoh, J. &lt;strong&gt;HTRA1 promoter polymorphism in wet age-related macular degeneration.&lt;/strong&gt; Science 314: 989-992, 2006.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17053108/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17053108&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1126/science.1133807&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17053108">DeWan et al. (2006)</a> studied 96 patients with wet ARMD from a cohort of Southeast Asians identified in Hong Kong and 130 age-matched control individuals who were ARMD-free. The ARMD cases and controls had a mean age of 74. Within this population <a href="#2" class="mim-tip-reference" title="DeWan, A., Liu, M., Hartman, S., Zhang, S. S.-M., Liu, D. T. L., Zhao, C., Tam, P. O. S., Chan, W. M., Lam, D. S. C., Snyder, M., Barnstable, C., Pang, C. P., Hoh, J. &lt;strong&gt;HTRA1 promoter polymorphism in wet age-related macular degeneration.&lt;/strong&gt; Science 314: 989-992, 2006.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17053108/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17053108&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1126/science.1133807&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17053108">DeWan et al. (2006)</a> identified a 10-fold increased risk for wet ARMD for individuals homozygous for the risk genotype (AA) of a single-nucleotide polymorphism, <a href="https://www.ensembl.org/Homo_sapiens/Variation/Summary?v=rs11200638;toggle_HGVS_names=open" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'dbSNP\', \'domain\': \'ensembl.org\'})">rs11200638</a>, located 512 basepairs upstream of the putative transcriptional start site of the HTRA1 gene (-512G-A; <a href="/entry/602194#0001">602194.0001</a>). Transfection studies suggested that the sequence change associated with the SNP enhances transcription of HTRA1 in individuals homozygous for the risk allele. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17053108" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#12" class="mim-tip-reference" title="Yang, Z., Camp, N. J., Sun, H., Tong, Z., Gibbs, D., Cameron, D. J., Chen, H., Zhao, Y., Pearson, E., Li, X., Chien, J., DeWan, A., Harmon, J., Bernstein, P. S., Shridhar, V., Zabriskie, N. A., Hoh, J., Howes, K., Zhang, K. &lt;strong&gt;A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration.&lt;/strong&gt; Science 314: 992-993, 2006.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17053109/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17053109&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1126/science.1133811&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17053109">Yang et al. (2006)</a> genotyped 581 ARMD cases and 309 normal controls in a Caucasian cohort in Utah and found that <a href="https://www.ensembl.org/Homo_sapiens/Variation/Summary?v=rs11200638;toggle_HGVS_names=open" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'dbSNP\', \'domain\': \'ensembl.org\'})">rs11200638</a> was the most likely causal variant for ARMD at the 10q26 locus. They estimated that the variant confers a population-attributable risk of 49.3%. Preliminary analysis of lymphocytes and retinal pigment epithelium from 4 ARMD patients revealed that the risk allele was associated with elevated expression levels of HTRA1 mRNA and protein. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17053109" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p><a href="#9" class="mim-tip-reference" title="Mori, K., Horie-Inoue, K., Kohda, M., Kawasaki, I., Gehlbach, P. L., Awata, T., Yoneya, S., Okazaki, Y., Inoue, S. &lt;strong&gt;Association of the HTRA1 gene variant with age-related macular degeneration in the Japanese population.&lt;/strong&gt; J. Hum. Genet. 52: 636-641, 2007.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17568988/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17568988&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1007/s10038-007-0162-1&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17568988">Mori et al. (2007)</a> found a significant association between the -512A allele and ARMD among 123 Japanese patients and 133 Japanese controls. The frequency of the risk A allele was 0.577 and 0.380 in patients and controls, respectively, yielding an odds ratio of 2.23 (p = 7.75 x 10(-6)). The results were more significant in a subset of 104 Japanese patients with wet ARMD (p = 5.96 x 10(-7)). The association was significant in both nonsmokers and smokers, and was more significant in nonsmokers. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17568988" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p><p>In a discussion of studies of the 10q26 ARMD locus, <a href="#1" class="mim-tip-reference" title="Allikmets, R., Dean, M. &lt;strong&gt;Bringing age-related macular degeneration into focus.&lt;/strong&gt; Nature Genet. 40: 820-821, 2008.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/18583975/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;18583975&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1038/ng0708-820&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="18583975">Allikmets and Dean (2008)</a> commented on the studies of <a href="#12" class="mim-tip-reference" title="Yang, Z., Camp, N. J., Sun, H., Tong, Z., Gibbs, D., Cameron, D. J., Chen, H., Zhao, Y., Pearson, E., Li, X., Chien, J., DeWan, A., Harmon, J., Bernstein, P. S., Shridhar, V., Zabriskie, N. A., Hoh, J., Howes, K., Zhang, K. &lt;strong&gt;A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration.&lt;/strong&gt; Science 314: 992-993, 2006.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17053109/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17053109&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1126/science.1133811&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17053109">Yang et al. (2006)</a> and <a href="#2" class="mim-tip-reference" title="DeWan, A., Liu, M., Hartman, S., Zhang, S. S.-M., Liu, D. T. L., Zhao, C., Tam, P. O. S., Chan, W. M., Lam, D. S. C., Snyder, M., Barnstable, C., Pang, C. P., Hoh, J. &lt;strong&gt;HTRA1 promoter polymorphism in wet age-related macular degeneration.&lt;/strong&gt; Science 314: 989-992, 2006.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17053108/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17053108&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1126/science.1133807&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17053108">DeWan et al. (2006)</a>, which suggested that the <a href="https://www.ensembl.org/Homo_sapiens/Variation/Summary?v=rs11200638;toggle_HGVS_names=open" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'dbSNP\', \'domain\': \'ensembl.org\'})">rs11200638</a> variant of HTRA1 was the sought-after functional variant and claimed that HTRA1 was the wet ARMD gene. They found 3 key problems arising from these 2 studies: (1) As the variant encoding A69S in the LOC387715 gene (<a href="https://www.ensembl.org/Homo_sapiens/Variation/Summary?v=rs10490924;toggle_HGVS_names=open" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'dbSNP\', \'domain\': \'ensembl.org\'})">rs10490924</a>; <a href="/entry/611313#0001">611313.0001</a>) is in almost complete linkage disequilibrium with <a href="https://www.ensembl.org/Homo_sapiens/Variation/Summary?v=rs11200638;toggle_HGVS_names=open" target="_blank" onclick="gtag(\'event\', \'mim_outbound\', {\'name\': \'dbSNP\', \'domain\': \'ensembl.org\'})">rs11200638</a> (D-prime = 0.99) (<a href="#2" class="mim-tip-reference" title="DeWan, A., Liu, M., Hartman, S., Zhang, S. S.-M., Liu, D. T. L., Zhao, C., Tam, P. O. S., Chan, W. M., Lam, D. S. C., Snyder, M., Barnstable, C., Pang, C. P., Hoh, J. &lt;strong&gt;HTRA1 promoter polymorphism in wet age-related macular degeneration.&lt;/strong&gt; Science 314: 989-992, 2006.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17053108/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17053108&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1126/science.1133807&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17053108">Dewan et al., 2006</a>), it is impossible to assign causality on the basis of allele frequencies alone; (2) the 10q26 locus does not harbor a wet ARMD gene, but rather a late ARMD, including both wet and dry subtypes, as shown by <a href="#10" class="mim-tip-reference" title="Rivera, A., Fisher, S. A., Fritsche, L. G., Keilhauer, C. N., Lichtner, P., Meitinger, T., Weber, B. H. &lt;strong&gt;Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.&lt;/strong&gt; Hum. Molec. Genet. 14: 3227-3236, 2005.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/16174643/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;16174643&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1093/hmg/ddi353&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="16174643">Rivera et al. (2005)</a>; and (3) subsequent studies failed to replicate the functional (gene expression) data (<a href="#6" class="mim-tip-reference" title="Kanda, A., Chen, W., Othman, M., Branham, K. E. H., Brooks, M., Khanna, R., He, S., Lyons, R., Abecasis, G. R., Swaroop, A. &lt;strong&gt;A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration.&lt;/strong&gt; Proc. Nat. Acad. Sci. 104: 16227-16232, 2007.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/17884985/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;17884985&lt;/a&gt;, &lt;a href=&quot;https://www.ncbi.nlm.nih.gov/pmc/?term=17884985[PMID]&amp;report=imagesdocsum&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed Image&#x27;, &#x27;domain&#x27;: &#x27;ncbi.nlm.nih.gov&#x27;})&quot;&gt;images&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1073/pnas.0703933104&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="17884985">Kanda et al., 2007</a>, <a href="#5" class="mim-tip-reference" title="Fritsche, L. G., Loenhardt, T., Janssen, A., Fisher, S. A., Rivera, A., Keilhauer, C. N., Weber, B. H. F. &lt;strong&gt;Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.&lt;/strong&gt; Nature Genet. 40: 892-896, 2008.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/18511946/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;18511946&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1038/ng.170&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="18511946">Fritsche et al., 2008</a>). <a href="https://pubmed.ncbi.nlm.nih.gov/?term=17053108+17053109+16174643+17884985+18583975+18511946" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<h4 href="#mimAnimalModelFold" id="mimAnimalModelToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
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<strong>Animal Model</strong>
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<p><a href="#4" class="mim-tip-reference" title="Francis, P. J., Appukuttan, B., Simmons, E., Landauer, N., Stoddard, J., Hamon, S., Ott, J., Ferguson, B., Klein, M., Stout, J. T., Neuringer, M. &lt;strong&gt;Rhesus monkeys and humans share common susceptibility genes for age-related macular diseases.&lt;/strong&gt; Hum. Molec. Genet. 17: 2673-2680, 2008.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/18535016/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;18535016&lt;/a&gt;, &lt;a href=&quot;https://www.ncbi.nlm.nih.gov/pmc/?term=18535016[PMID]&amp;report=imagesdocsum&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed Image&#x27;, &#x27;domain&#x27;: &#x27;ncbi.nlm.nih.gov&#x27;})&quot;&gt;images&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1093/hmg/ddn167&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="18535016">Francis et al. (2008)</a> genotyped 137 unrelated rhesus macaques, 81 with and 56 without macular drusen, and identified a variant in the Htra1 gene that was significantly associated with affected status. Functional analysis of the polymorphic variant showed a 2-fold increase in gene expression, supporting a role in pathogenesis. <a href="#4" class="mim-tip-reference" title="Francis, P. J., Appukuttan, B., Simmons, E., Landauer, N., Stoddard, J., Hamon, S., Ott, J., Ferguson, B., Klein, M., Stout, J. T., Neuringer, M. &lt;strong&gt;Rhesus monkeys and humans share common susceptibility genes for age-related macular diseases.&lt;/strong&gt; Hum. Molec. Genet. 17: 2673-2680, 2008.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/18535016/&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed&#x27;, &#x27;domain&#x27;: &#x27;pubmed.ncbi.nlm.nih.gov&#x27;})&quot;&gt;18535016&lt;/a&gt;, &lt;a href=&quot;https://www.ncbi.nlm.nih.gov/pmc/?term=18535016[PMID]&amp;report=imagesdocsum&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;name&#x27;: &#x27;PubMed Image&#x27;, &#x27;domain&#x27;: &#x27;ncbi.nlm.nih.gov&#x27;})&quot;&gt;images&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1093/hmg/ddn167&quot; target=&quot;_blank&quot; onclick=&quot;gtag(&#x27;event&#x27;, &#x27;mim_outbound&#x27;, {&#x27;destination&#x27;: &#x27;Publisher&#x27;})&quot;&gt;Full Text&lt;/a&gt;]" pmid="18535016">Francis et al. (2008)</a> stated that this was the first evidence that humans and macaques share the same genetic susceptibility factors for common complex disease. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=18535016" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})"><span class="glyphicon glyphicon-plus-sign mim-tip-hint" title="Click this 'reference-plus' icon to see articles related to this paragraph in PubMed."></span></a></p>
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<a id="references"class="mim-anchor"></a>
<h4 href="#mimReferencesFold" id="mimReferencesToggle" class="mimTriangleToggle" style="cursor: pointer;" data-toggle="collapse">
<span class="mim-font">
<span id="mimReferencesToggleTriangle" class="small mimTextToggleTriangle">&#9660;</span>
<strong>REFERENCES</strong>
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</div>
<div id="mimReferencesFold" class="collapse in mimTextToggleFold">
<ol>
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<a id="1" class="mim-anchor"></a>
<a id="Allikmets2008" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Allikmets, R., Dean, M.
<strong>Bringing age-related macular degeneration into focus.</strong>
Nature Genet. 40: 820-821, 2008.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/18583975/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">18583975</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=18583975" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1038/ng0708-820" target="_blank">Full Text</a>]
</p>
</div>
</li>
<li>
<a id="2" class="mim-anchor"></a>
<a id="DeWan2006" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
DeWan, A., Liu, M., Hartman, S., Zhang, S. S.-M., Liu, D. T. L., Zhao, C., Tam, P. O. S., Chan, W. M., Lam, D. S. C., Snyder, M., Barnstable, C., Pang, C. P., Hoh, J.
<strong>HTRA1 promoter polymorphism in wet age-related macular degeneration.</strong>
Science 314: 989-992, 2006.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/17053108/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">17053108</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17053108" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1126/science.1133807" target="_blank">Full Text</a>]
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<a id="3" class="mim-anchor"></a>
<a id="Fisher2005" class="mim-anchor"></a>
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Fisher, S. A., Abecasis, G. R., Yashar, B. M., Zareparsi, S., Swaroop, A., Iyengar, S. K., Klein, B. E. K., Klein, R., Lee, K. E., Majewski, J., Schultz, D. W., Klein, M. L., and 13 others.
<strong>Meta-analysis of genome scans of age-related macular degeneration.</strong>
Hum. Molec. Genet. 14: 2257-2264, 2005.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/15987700/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">15987700</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=15987700" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1093/hmg/ddi230" target="_blank">Full Text</a>]
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<a id="4" class="mim-anchor"></a>
<a id="Francis2008" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Francis, P. J., Appukuttan, B., Simmons, E., Landauer, N., Stoddard, J., Hamon, S., Ott, J., Ferguson, B., Klein, M., Stout, J. T., Neuringer, M.
<strong>Rhesus monkeys and humans share common susceptibility genes for age-related macular diseases.</strong>
Hum. Molec. Genet. 17: 2673-2680, 2008.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/18535016/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">18535016</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=18535016[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=18535016" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1093/hmg/ddn167" target="_blank">Full Text</a>]
</p>
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<a id="5" class="mim-anchor"></a>
<a id="Fritsche2008" class="mim-anchor"></a>
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<p class="mim-text-font">
Fritsche, L. G., Loenhardt, T., Janssen, A., Fisher, S. A., Rivera, A., Keilhauer, C. N., Weber, B. H. F.
<strong>Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.</strong>
Nature Genet. 40: 892-896, 2008.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/18511946/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">18511946</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=18511946" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1038/ng.170" target="_blank">Full Text</a>]
</p>
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<a id="Kanda2007" class="mim-anchor"></a>
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<p class="mim-text-font">
Kanda, A., Chen, W., Othman, M., Branham, K. E. H., Brooks, M., Khanna, R., He, S., Lyons, R., Abecasis, G. R., Swaroop, A.
<strong>A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration.</strong>
Proc. Nat. Acad. Sci. 104: 16227-16232, 2007.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/17884985/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">17884985</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=17884985[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17884985" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1073/pnas.0703933104" target="_blank">Full Text</a>]
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<a id="7" class="mim-anchor"></a>
<a id="Kenealy2004" class="mim-anchor"></a>
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Kenealy, S. J., Schmidt, S., Agarwal, A., Postel, E. A., De La Paz, M. A., Pericak-Vance, M. A., Haines, J. L.
<strong>Linkage analysis for age-related macular degeneration supports a gene on chromosome 10q26.</strong>
Molec. Vis. 10: 57-61, 2004.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/14758336/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">14758336</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=14758336" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
</p>
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<a id="8" class="mim-anchor"></a>
<a id="Majewski2003" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Majewski, J., Schultz, D. W., Weleber, R. G., Schain, M. B., Edwards, A. O., Matise, T. C., Acott, T. S., Ott, J., Klein, M. L.
<strong>Age-related macular degeneration--a genome scan in extended families.</strong>
Am. J. Hum. Genet. 73: 540-550, 2003.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/12900797/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">12900797</a>, <a href="https://www.ncbi.nlm.nih.gov/pmc/?term=12900797[PMID]&report=imagesdocsum" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Image', 'domain': 'ncbi.nlm.nih.gov'})">images</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=12900797" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1086/377701" target="_blank">Full Text</a>]
</p>
</div>
</li>
<li>
<a id="9" class="mim-anchor"></a>
<a id="Mori2007" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Mori, K., Horie-Inoue, K., Kohda, M., Kawasaki, I., Gehlbach, P. L., Awata, T., Yoneya, S., Okazaki, Y., Inoue, S.
<strong>Association of the HTRA1 gene variant with age-related macular degeneration in the Japanese population.</strong>
J. Hum. Genet. 52: 636-641, 2007.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/17568988/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">17568988</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17568988" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1007/s10038-007-0162-1" target="_blank">Full Text</a>]
</p>
</div>
</li>
<li>
<a id="10" class="mim-anchor"></a>
<a id="Rivera2005" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Rivera, A., Fisher, S. A., Fritsche, L. G., Keilhauer, C. N., Lichtner, P., Meitinger, T., Weber, B. H.
<strong>Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.</strong>
Hum. Molec. Genet. 14: 3227-3236, 2005.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/16174643/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">16174643</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=16174643" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1093/hmg/ddi353" target="_blank">Full Text</a>]
</p>
</div>
</li>
<li>
<a id="11" class="mim-anchor"></a>
<a id="Seddon2003" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Seddon, J. M., Santangelo, S. L., Book, K., Chong, S., Cote, J.
<strong>A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions.</strong>
Am. J. Hum. Genet. 73: 780-790, 2003.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/12945014/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">12945014</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=12945014" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1086/378505" target="_blank">Full Text</a>]
</p>
</div>
</li>
<li>
<a id="12" class="mim-anchor"></a>
<a id="Yang2006" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Yang, Z., Camp, N. J., Sun, H., Tong, Z., Gibbs, D., Cameron, D. J., Chen, H., Zhao, Y., Pearson, E., Li, X., Chien, J., DeWan, A., Harmon, J., Bernstein, P. S., Shridhar, V., Zabriskie, N. A., Hoh, J., Howes, K., Zhang, K.
<strong>A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration.</strong>
Science 314: 992-993, 2006.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/17053109/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">17053109</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=17053109" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1126/science.1133811" target="_blank">Full Text</a>]
</p>
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Marla J. F. O'Neill - updated : 8/5/2010
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Anne M. Stumpf - updated : 9/9/2008<br>Cassandra L. Kniffin - updated : 7/31/2007<br>Victor A. McKusick - updated : 10/6/2006<br>Anne M. Stumpf - updated : 5/26/2006
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Victor A. McKusick : 5/25/2006
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alopez : 12/14/2022
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alopez : 10/05/2016<br>carol : 06/22/2016<br>alopez : 7/31/2012<br>terry : 7/23/2012<br>carol : 2/28/2011<br>wwang : 8/5/2010<br>alopez : 9/9/2008<br>carol : 10/16/2007<br>carol : 10/16/2007<br>alopez : 8/9/2007<br>wwang : 7/31/2007<br>carol : 5/14/2007<br>carol : 4/11/2007<br>carol : 3/8/2007<br>alopez : 1/16/2007<br>alopez : 1/12/2007<br>alopez : 1/11/2007<br>terry : 11/3/2006<br>alopez : 10/6/2006<br>wwang : 8/11/2006<br>alopez : 6/1/2006<br>alopez : 5/26/2006<br>alopez : 5/26/2006
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<h3>
<span class="mim-font">
<strong>#</strong> 610149
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<h3>
<span class="mim-font">
MACULAR DEGENERATION, AGE-RELATED, 7; ARMD7
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Other entities represented in this entry:
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<span class="h3 mim-font">
MACULAR DEGENERATION, AGE-RELATED, NEOVASCULAR TYPE, SUSCEPTIBILITY TO, INCLUDED
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MACULAR DEGENERATION, AGE-RELATED, WET TYPE, SUSCEPTIBILITY TO, INCLUDED
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<span class="mim-text-font">
<strong>DO:</strong> 0110019; &nbsp;
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<h4>
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<strong>Phenotype-Gene Relationships</strong>
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<table class="table table-bordered table-condensed small mim-table-padding">
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<th>
Location
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<th>
Phenotype
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<th>
Phenotype <br /> MIM number
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Inheritance
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Phenotype <br /> mapping key
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Gene/Locus
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Gene/Locus <br /> MIM number
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<span class="mim-font">
10q26.13
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{Macular degeneration, age-related, 7}
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<span class="mim-font">
610149
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</span>
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<span class="mim-font">
3
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HTRA1
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602194
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10q26.13
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<span class="mim-font">
{Macular degeneration, age-related, neovascular type}
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<span class="mim-font">
610149
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</span>
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<span class="mim-font">
3
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<span class="mim-font">
HTRA1
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<span class="mim-font">
602194
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<span class="mim-font">
<strong>TEXT</strong>
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<p>A number sign (#) is used with this entry because of evidence that susceptibility to age-related macular degeneration-7 (ARMD7) is conferred by variation in the HTRA1 gene (602194) on chromosome 10q26.</p><p>See also ARMD8 (613778) for a discussion of the relationship of another gene in the 10q26 region, ARMS2 (611313; also known as LOC387715), and susceptibility to ARMD.</p><p>For a phenotypic description and a discussion of genetic heterogeneity of age-related macular degeneration, see 603075.</p>
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<strong>Mapping</strong>
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<p>Several studies had suggested specific ARMD susceptibility genes in the 10q26 region (e.g., Majewski et al. (2003), Seddon et al. (2003), Kenealy et al. (2004), Fisher et al. (2005)). </p>
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<span class="mim-font">
<strong>Molecular Genetics</strong>
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<p>The neovascular, or wet, type of ARMD is more prevalent among Asians than among Caucasians, and the soft indistinct drusen characteristic of dry, or nonneovascular, ARMD are rarely seen in Asian individuals. To identify novel genetic variants that predispose individuals to the wet ARMD phenotype, DeWan et al. (2006) studied 96 patients with wet ARMD from a cohort of Southeast Asians identified in Hong Kong and 130 age-matched control individuals who were ARMD-free. The ARMD cases and controls had a mean age of 74. Within this population DeWan et al. (2006) identified a 10-fold increased risk for wet ARMD for individuals homozygous for the risk genotype (AA) of a single-nucleotide polymorphism, rs11200638, located 512 basepairs upstream of the putative transcriptional start site of the HTRA1 gene (-512G-A; 602194.0001). Transfection studies suggested that the sequence change associated with the SNP enhances transcription of HTRA1 in individuals homozygous for the risk allele. </p><p>Yang et al. (2006) genotyped 581 ARMD cases and 309 normal controls in a Caucasian cohort in Utah and found that rs11200638 was the most likely causal variant for ARMD at the 10q26 locus. They estimated that the variant confers a population-attributable risk of 49.3%. Preliminary analysis of lymphocytes and retinal pigment epithelium from 4 ARMD patients revealed that the risk allele was associated with elevated expression levels of HTRA1 mRNA and protein. </p><p>Mori et al. (2007) found a significant association between the -512A allele and ARMD among 123 Japanese patients and 133 Japanese controls. The frequency of the risk A allele was 0.577 and 0.380 in patients and controls, respectively, yielding an odds ratio of 2.23 (p = 7.75 x 10(-6)). The results were more significant in a subset of 104 Japanese patients with wet ARMD (p = 5.96 x 10(-7)). The association was significant in both nonsmokers and smokers, and was more significant in nonsmokers. </p><p>In a discussion of studies of the 10q26 ARMD locus, Allikmets and Dean (2008) commented on the studies of Yang et al. (2006) and DeWan et al. (2006), which suggested that the rs11200638 variant of HTRA1 was the sought-after functional variant and claimed that HTRA1 was the wet ARMD gene. They found 3 key problems arising from these 2 studies: (1) As the variant encoding A69S in the LOC387715 gene (rs10490924; 611313.0001) is in almost complete linkage disequilibrium with rs11200638 (D-prime = 0.99) (Dewan et al., 2006), it is impossible to assign causality on the basis of allele frequencies alone; (2) the 10q26 locus does not harbor a wet ARMD gene, but rather a late ARMD, including both wet and dry subtypes, as shown by Rivera et al. (2005); and (3) subsequent studies failed to replicate the functional (gene expression) data (Kanda et al., 2007, Fritsche et al., 2008). </p>
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<h4>
<span class="mim-font">
<strong>Animal Model</strong>
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</h4>
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<p>Francis et al. (2008) genotyped 137 unrelated rhesus macaques, 81 with and 56 without macular drusen, and identified a variant in the Htra1 gene that was significantly associated with affected status. Functional analysis of the polymorphic variant showed a 2-fold increase in gene expression, supporting a role in pathogenesis. Francis et al. (2008) stated that this was the first evidence that humans and macaques share the same genetic susceptibility factors for common complex disease. </p>
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<h4>
<span class="mim-font">
<strong>REFERENCES</strong>
</span>
</h4>
<div>
<p />
</div>
<div>
<ol>
<li>
<p class="mim-text-font">
Allikmets, R., Dean, M.
<strong>Bringing age-related macular degeneration into focus.</strong>
Nature Genet. 40: 820-821, 2008.
[PubMed: 18583975]
[Full Text: https://doi.org/10.1038/ng0708-820]
</p>
</li>
<li>
<p class="mim-text-font">
DeWan, A., Liu, M., Hartman, S., Zhang, S. S.-M., Liu, D. T. L., Zhao, C., Tam, P. O. S., Chan, W. M., Lam, D. S. C., Snyder, M., Barnstable, C., Pang, C. P., Hoh, J.
<strong>HTRA1 promoter polymorphism in wet age-related macular degeneration.</strong>
Science 314: 989-992, 2006.
[PubMed: 17053108]
[Full Text: https://doi.org/10.1126/science.1133807]
</p>
</li>
<li>
<p class="mim-text-font">
Fisher, S. A., Abecasis, G. R., Yashar, B. M., Zareparsi, S., Swaroop, A., Iyengar, S. K., Klein, B. E. K., Klein, R., Lee, K. E., Majewski, J., Schultz, D. W., Klein, M. L., and 13 others.
<strong>Meta-analysis of genome scans of age-related macular degeneration.</strong>
Hum. Molec. Genet. 14: 2257-2264, 2005.
[PubMed: 15987700]
[Full Text: https://doi.org/10.1093/hmg/ddi230]
</p>
</li>
<li>
<p class="mim-text-font">
Francis, P. J., Appukuttan, B., Simmons, E., Landauer, N., Stoddard, J., Hamon, S., Ott, J., Ferguson, B., Klein, M., Stout, J. T., Neuringer, M.
<strong>Rhesus monkeys and humans share common susceptibility genes for age-related macular diseases.</strong>
Hum. Molec. Genet. 17: 2673-2680, 2008.
[PubMed: 18535016]
[Full Text: https://doi.org/10.1093/hmg/ddn167]
</p>
</li>
<li>
<p class="mim-text-font">
Fritsche, L. G., Loenhardt, T., Janssen, A., Fisher, S. A., Rivera, A., Keilhauer, C. N., Weber, B. H. F.
<strong>Age-related macular degeneration is associated with an unstable ARMS2 (LOC387715) mRNA.</strong>
Nature Genet. 40: 892-896, 2008.
[PubMed: 18511946]
[Full Text: https://doi.org/10.1038/ng.170]
</p>
</li>
<li>
<p class="mim-text-font">
Kanda, A., Chen, W., Othman, M., Branham, K. E. H., Brooks, M., Khanna, R., He, S., Lyons, R., Abecasis, G. R., Swaroop, A.
<strong>A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration.</strong>
Proc. Nat. Acad. Sci. 104: 16227-16232, 2007.
[PubMed: 17884985]
[Full Text: https://doi.org/10.1073/pnas.0703933104]
</p>
</li>
<li>
<p class="mim-text-font">
Kenealy, S. J., Schmidt, S., Agarwal, A., Postel, E. A., De La Paz, M. A., Pericak-Vance, M. A., Haines, J. L.
<strong>Linkage analysis for age-related macular degeneration supports a gene on chromosome 10q26.</strong>
Molec. Vis. 10: 57-61, 2004.
[PubMed: 14758336]
</p>
</li>
<li>
<p class="mim-text-font">
Majewski, J., Schultz, D. W., Weleber, R. G., Schain, M. B., Edwards, A. O., Matise, T. C., Acott, T. S., Ott, J., Klein, M. L.
<strong>Age-related macular degeneration--a genome scan in extended families.</strong>
Am. J. Hum. Genet. 73: 540-550, 2003.
[PubMed: 12900797]
[Full Text: https://doi.org/10.1086/377701]
</p>
</li>
<li>
<p class="mim-text-font">
Mori, K., Horie-Inoue, K., Kohda, M., Kawasaki, I., Gehlbach, P. L., Awata, T., Yoneya, S., Okazaki, Y., Inoue, S.
<strong>Association of the HTRA1 gene variant with age-related macular degeneration in the Japanese population.</strong>
J. Hum. Genet. 52: 636-641, 2007.
[PubMed: 17568988]
[Full Text: https://doi.org/10.1007/s10038-007-0162-1]
</p>
</li>
<li>
<p class="mim-text-font">
Rivera, A., Fisher, S. A., Fritsche, L. G., Keilhauer, C. N., Lichtner, P., Meitinger, T., Weber, B. H.
<strong>Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk.</strong>
Hum. Molec. Genet. 14: 3227-3236, 2005.
[PubMed: 16174643]
[Full Text: https://doi.org/10.1093/hmg/ddi353]
</p>
</li>
<li>
<p class="mim-text-font">
Seddon, J. M., Santangelo, S. L., Book, K., Chong, S., Cote, J.
<strong>A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions.</strong>
Am. J. Hum. Genet. 73: 780-790, 2003.
[PubMed: 12945014]
[Full Text: https://doi.org/10.1086/378505]
</p>
</li>
<li>
<p class="mim-text-font">
Yang, Z., Camp, N. J., Sun, H., Tong, Z., Gibbs, D., Cameron, D. J., Chen, H., Zhao, Y., Pearson, E., Li, X., Chien, J., DeWan, A., Harmon, J., Bernstein, P. S., Shridhar, V., Zabriskie, N. A., Hoh, J., Howes, K., Zhang, K.
<strong>A variant of the HTRA1 gene increases susceptibility to age-related macular degeneration.</strong>
Science 314: 992-993, 2006.
[PubMed: 17053109]
[Full Text: https://doi.org/10.1126/science.1133811]
</p>
</li>
</ol>
<div>
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Contributors:
</span>
</div>
<div class="col-lg-6 col-md-6 col-sm-6 col-xs-6">
<span class="mim-text-font">
Marla J. F. O&#x27;Neill - updated : 8/5/2010<br>Anne M. Stumpf - updated : 9/9/2008<br>Cassandra L. Kniffin - updated : 7/31/2007<br>Victor A. McKusick - updated : 10/6/2006<br>Anne M. Stumpf - updated : 5/26/2006
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Victor A. McKusick : 5/25/2006
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