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<title>
Entry
- *601589 - RAS p21 PROTEIN ACTIVATOR 2; RASA2
- OMIM
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<span class="h4">*601589</span>
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<strong>Table of Contents</strong>
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<a href="#cloning">Cloning and Expression</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="#references"><strong>References</strong></a>
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<a href="#creationDate"><strong>Creation Date</strong></a>
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<div><a href="https://hprd.org/summary?hprd_id=03351&isoform_id=03351_1&isoform_name=Isoform_1" class="mim-tip-hint" title="The Human Protein Reference Database; manually extracted and visually depicted information on human proteins." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HPRD', 'domain': 'hprd.org'})">HPRD</a></div>
<div><a href="https://www.proteinatlas.org/search/RASA2" class="mim-tip-hint" title="The Human Protein Atlas contains information for a large majority of all human protein-coding genes regarding the expression and localization of the corresponding proteins based on both RNA and protein data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HumanProteinAtlas', 'domain': 'proteinatlas.org'})">Human Protein Atlas</a></div>
<div><a href="https://www.ncbi.nlm.nih.gov/protein/1060909,1513026,1513028,1871475,4191600,12545408,62087902,119599404,119599405,158257464,194375039,519668674,747019245,747019247,767927335,1370484864,2217345310,2462591674,2462591676" class="mim-tip-hint" title="NCBI protein data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Protein', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Protein</a></div>
<div><a href="https://www.uniprot.org/uniprotkb/Q15283" class="mim-tip-hint" title="Comprehensive protein sequence and functional information, including supporting data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UniProt', 'domain': 'uniprot.org'})">UniProt</a></div>
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&nbsp;
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<div id="mimGeneInfoLinksFold" class="panel-collapse collapse mimLinksFold" role="tabpanel">
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<div><a href="http://biogps.org/#goto=genereport&id=5922" class="mim-tip-hint" title="The Gene Portal Hub; customizable portal of gene and protein function information." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'BioGPS', 'domain': 'biogps.org'})">BioGPS</a></div>
<div><a href="https://www.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=ENSG00000155903;t=ENST00000286364" class="mim-tip-hint" title="Orthologs, paralogs, regulatory regions, and splice variants." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl</a></div>
<div><a href="https://www.genecards.org/cgi-bin/carddisp.pl?gene=RASA2" class="mim-tip-hint" title="The Human Genome Compendium; web-based cards integrating automatically mined information on human genes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GeneCards', 'domain': 'genecards.org'})">GeneCards</a></div>
<div><a href="http://amigo.geneontology.org/amigo/search/annotation?q=RASA2" class="mim-tip-hint" title="Terms, defined using controlled vocabulary, representing gene product properties (biologic process, cellular component, molecular function) across species." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GeneOntology', 'domain': 'amigo.geneontology.org'})">Gene Ontology</a></div>
<div><a href="https://www.genome.jp/dbget-bin/www_bget?hsa+5922" class="mim-tip-hint" title="Kyoto Encyclopedia of Genes and Genomes; diagrams of signaling pathways." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'KEGG', 'domain': 'genome.jp'})">KEGG</a></div>
<dd><a href="http://v1.marrvel.org/search/gene/RASA2" class="mim-tip-hint" title="Model organism Aggregated Resources for Rare Variant ExpLoration." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MARRVEL', 'domain': 'marrvel.org'})">MARRVEL</a></dd>
<dd><a href="https://monarchinitiative.org/NCBIGene:5922" class="mim-tip-hint" title="Monarch Initiative." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Monarch', 'domain': 'monarchinitiative.org'})">Monarch</a></dd>
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<div><a href="https://genome.ucsc.edu/cgi-bin/hgGene?db=hg38&hgg_chrom=chr3&hgg_gene=ENST00000286364.9&hgg_start=141487027&hgg_end=141615344&hgg_type=knownGene" class="mim-tip-hint" title="UCSC Genome Bioinformatics; gene-specific structure and function information with links to other databases." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UCSC', 'domain': 'genome.ucsc.edu'})">UCSC</a></div>
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<div><a href="https://search.clinicalgenome.org/kb/genes/HGNC:9872" class="mim-tip-hint" title="A ClinGen curated resource of ratings for the strength of evidence supporting or refuting the clinical validity of the claim(s) that variation in a particular gene causes disease." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinGen Validity', 'domain': 'search.clinicalgenome.org'})">ClinGen Validity</a></div>
<div><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=601589[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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<span id="mimVariationLinksToggleTriangle" class="small mimSingletonTriangle" style="color: #337CB5">&#9660;</span> Variation
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<div><a href="https://www.ncbi.nlm.nih.gov/clinvar?term=601589[MIM]" class="mim-tip-hint" title="ClinVar aggregates information about sequence variation and its relationship to human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinVar', 'domain': 'ncbi.nlm.nih.gov'})">ClinVar</a></div>
<div><a href="https://www.deciphergenomics.org/gene/RASA2/overview/clinical-info" class="mim-tip-hint" title="DECIPHER" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'DECIPHER', 'domain': 'DECIPHER'})">DECIPHER</a></div>
<div><a href="https://gnomad.broadinstitute.org/gene/ENSG00000155903" class="mim-tip-hint" title="The Genome Aggregation Database (gnomAD), Broad Institute." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'gnomAD', 'domain': 'gnomad.broadinstitute.org'})">gnomAD</a></div>
<div><a href="https://www.ebi.ac.uk/gwas/search?query=RASA2" class="mim-tip-hint" title="GWAS Catalog; NHGRI-EBI Catalog of published genome-wide association studies." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GWAS Catalog', 'domain': 'gwascatalog.org'})">GWAS Catalog&nbsp;</a></div>
<div><a href="https://www.gwascentral.org/search?q=RASA2" class="mim-tip-hint" title="GWAS Central; summary level genotype-to-phenotype information from genetic association studies." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'GWAS Central', 'domain': 'gwascentral.org'})">GWAS Central&nbsp;</a></div>
<div><a href="https://evs.gs.washington.edu/EVS/PopStatsServlet?searchBy=Gene+Hugo&target=RASA2&upstreamSize=0&downstreamSize=0&x=0&y=0" class="mim-tip-hint" title="National Heart, Lung, and Blood Institute Exome Variant Server." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NHLBI EVS', 'domain': 'evs.gs.washington.edu'})">NHLBI EVS</a></div>
<div><a href="https://www.pharmgkb.org/gene/PA34233" class="mim-tip-hint" title="Pharmacogenomics Knowledge Base; curated and annotated information regarding the effects of human genetic variations on drug response." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PharmGKB', 'domain': 'pharmgkb.org'})">PharmGKB</a></div>
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<div><a href="https://www.alliancegenome.org/gene/HGNC:9872" 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="https://flybase.org/reports/FBgn0004390.html" class="mim-tip-hint" title="A Database of Drosophila Genes and Genomes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'FlyBase', 'domain': 'flybase.org'})">FlyBase</a></div>
<div><a href="https://www.mousephenotype.org/data/genes/MGI:2149960" class="mim-tip-hint" title="International Mouse Phenotyping Consortium." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'IMPC', 'domain': 'knockoutmouse.org'})">IMPC</a></div>
<div><a href="http://v1.marrvel.org/search/gene/RASA2#HomologGenesPanel" class="mim-tip-hint" title="Model organism Aggregated Resources for Rare Variant ExpLoration." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MARRVEL', 'domain': 'marrvel.org'})">MARRVEL</a></div>
<div><a href="http://www.informatics.jax.org/marker/MGI:2149960" class="mim-tip-hint" title="Mouse Genome Informatics; international database resource for the laboratory mouse, including integrated genetic, genomic, and biological data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MGI Mouse Gene', 'domain': 'informatics.jax.org'})">MGI Mouse Gene</a></div>
<div><a href="https://www.mmrrc.org/catalog/StrainCatalogSearchForm.php?search_query=" class="mim-tip-hint" title="Mutant Mouse Resource & Research Centers." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MMRRC', 'domain': 'mmrrc.org'})">MMRRC</a></div>
<div><a href="https://www.ncbi.nlm.nih.gov/gene/5922/ortholog/" class="mim-tip-hint" title="Orthologous genes at NCBI." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Orthologs', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Orthologs</a></div>
<div><a href="https://www.orthodb.org/?ncbi=5922" class="mim-tip-hint" title="Hierarchical catalogue of orthologs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrthoDB', 'domain': 'orthodb.org'})">OrthoDB</a></div>
<div><a href="https://wormbase.org/db/gene/gene?name=WBGene00001515;class=Gene" class="mim-tip-hint" title="Database of the biology and genome of Caenorhabditis elegans and related nematodes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name'{'name': 'Wormbase Gene', 'domain': 'wormbase.org'})">Wormbase Gene</a></div>
<div><a href="https://zfin.org/ZDB-GENE-030131-5660" class="mim-tip-hint" title="The Zebrafish Model Organism Database." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ZFin', 'domain': 'zfin.org'})">ZFin</a></div>
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<div><a href="https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+hsa:5922" class="mim-tip-hint" title="Kyoto Encyclopedia of Genes and Genomes; diagrams of signaling pathways." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'KEGG', 'domain': 'genome.jp'})">KEGG</a></div>
<div><a href="https://reactome.org/content/query?q=RASA2&species=Homo+sapiens&types=Reaction&types=Pathway&cluster=true" class="definition" title="Protein-specific information in the context of relevant cellular pathways." target="_blank" onclick="gtag('event', 'mim_outbound', {{'name': 'Reactome', 'domain': 'reactome.org'}})">Reactome</a></div>
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<a id="title" class="mim-anchor"></a>
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<a id="number" class="mim-anchor"></a>
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&nbsp;
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<div>
<span class="h3">
<span class="mim-font mim-tip-hint" title="Gene description">
<span class="text-danger"><strong>*</strong></span>
601589
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<div>
<a id="preferredTitle" class="mim-anchor"></a>
<h3>
<span class="mim-font">
RAS p21 PROTEIN ACTIVATOR 2; RASA2
</span>
</h3>
</div>
<div>
<br />
</div>
<div>
<a id="alternativeTitles" class="mim-anchor"></a>
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<p>
<span class="mim-font">
<em>Alternative titles; symbols</em>
</span>
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<h4>
<span class="mim-font">
GTPase-ACTIVATING PROTEIN OF RAS; GAP1M
</span>
</h4>
</div>
</div>
<div>
<br />
</div>
</div>
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<a id="approvedGeneSymbols" class="mim-anchor"></a>
<p>
<span class="mim-text-font">
<strong><em>HGNC Approved Gene Symbol: <a href="https://www.genenames.org/tools/search/#!/genes?query=RASA2" class="mim-tip-hint" title="HUGO Gene Nomenclature Committee." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HGNC', 'domain': 'genenames.org'})">RASA2</a></em></strong>
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<a id="cytogeneticLocation" class="mim-anchor"></a>
<p>
<span class="mim-text-font">
<strong>
<em>
Cytogenetic location: <a href="/geneMap/3/737?start=-3&limit=10&highlight=737">3q23</a>
&nbsp;
Genomic coordinates <span class="small">(GRCh38)</span> : <a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr3:141487027-141615344&dgv=pack&knownGene=pack&omimGene=pack" class="mim-tip-hint" title="UCSC Genome Browser; reference sequences and working draft assemblies for a large collection of genomes." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'UCSC Genome Browser', 'domain': 'genome.ucsc.edu'})">3:141,487,027-141,615,344</a> </span>
</em>
</strong>
<a href="https://www.ncbi.nlm.nih.gov/" target="_blank" class="small"> (from NCBI) </a>
</span>
</p>
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<br />
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<span class="mim-tip-floating" qtip_title="<strong>Looking For More References?</strong>" qtip_text="Click the 'reference plus' icon &lt;span class='glyphicon glyphicon-plus-sign'&gt;&lt;/span&gt at the end of each OMIM text paragraph to see more references related to the content of the preceding paragraph.">
<strong>TEXT</strong>
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<strong>Cloning and Expression</strong>
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<p><a href="#5" class="mim-tip-reference" title="Maekawa, M., Li, S., Iwamatsu, A., Morishita, T., Yokota, K., Imai, Y., Kohsaka, S., Nakamura, S., Hattori, S. &lt;strong&gt;A novel mammalian Ras GTPase-activating protein which has phospholipid-binding and Btk homology regions.&lt;/strong&gt; Molec. Cell. Biol. 14: 6879-6885, 1994.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/7935405/&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;7935405&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1128/mcb.14.10.6879-6885.1994&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="7935405">Maekawa et al. (1994)</a> isolated a mammalian GTPase-activating protein of RAS from rat (GAP1M) that shows sequence similarity to the suppressor of RAS (see <a href="/entry/190020">190020</a>) function in Drosophila, known as Gap1 (<a href="#3" class="mim-tip-reference" title="Gaul, U., Mardon, G., Rubin, G. M. &lt;strong&gt;A putative Ras GTPase activating protein acts as a negative regulator of signaling by the Sevenless receptor tyrosine kinase.&lt;/strong&gt; Cell 68: 1007-1019, 1992.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/1547500/&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;1547500&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1016/0092-8674(92)90073-l&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="1547500">Gaul et al., 1992</a>). Expression was relatively high in brain, placenta, and kidney but lower in other tissues. A recombinantly expressed protein containing the GAP-related domain was shown to stimulate GTPase activity of RAS. <a href="https://pubmed.ncbi.nlm.nih.gov/?term=1547500+7935405" 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="#4" class="mim-tip-reference" title="Li, S., Satoh, H., Watanabe, T., Nakamura, S., Hattori, S. &lt;strong&gt;cDNA cloning and chromosomal mapping of a novel human GAP (GAP1M), a GTPase-activating protein of Ras.&lt;/strong&gt; Genomics 35: 625-627, 1996.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/8812506/&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;8812506&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1006/geno.1996.0412&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="8812506">Li et al. (1996)</a> isolated the human homolog of rat GAP1M from a brain cDNA library. The deduced 853-amino acid protein is 89.4% identical to the rat protein. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8812506" 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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<strong>Mapping</strong>
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<p>Using a panel of somatic cell hybrid DNAs, <a href="#4" class="mim-tip-reference" title="Li, S., Satoh, H., Watanabe, T., Nakamura, S., Hattori, S. &lt;strong&gt;cDNA cloning and chromosomal mapping of a novel human GAP (GAP1M), a GTPase-activating protein of Ras.&lt;/strong&gt; Genomics 35: 625-627, 1996.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/8812506/&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;8812506&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1006/geno.1996.0412&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="8812506">Li et al. (1996)</a> mapped the human GAP1M gene to chromosome 3. By fluorescence in situ hybridization, they mapped GAP1M to chromosome 3q22-q23. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8812506" 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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<strong>Molecular Genetics</strong>
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<p><strong><em>Somatic Mutation</em></strong></p><p>
<a href="#1" class="mim-tip-reference" title="Arafeh, R., Qutob, N., Emmanuel, R., Keren-Paz, A., Madore, J., Elkahloun, A., Wilmott, J. S., Gartner, J. J., Di Pizio, A., Winograd-Katz, S., Sindiri, S., Rotkopf, R., and 16 others. &lt;strong&gt;Recurrent inactivating RASA2 mutations in melanoma.&lt;/strong&gt; Nature Genet. 47: 1408-1410, 2015.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/26502337/&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;26502337&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1038/ng.3427&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="26502337">Arafeh et al. (2015)</a> analyzed 501 melanoma (see <a href="/entry/155600">155600</a>) exomes and found that RASA2 was mutated in 5% of melanomas. Recurrent loss-of-function mutations in RASA2 were found to increase RAS activation and melanoma cell growth and migration. RASA2 expression was lost in at least 30% of human melanomas analyzed and was associated with reduced patient survival. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=26502337" 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><strong><em>Associations Pending Confirmation</em></strong></p><p>
Among 27 Noonan syndrome (see <a href="/entry/163950">163950</a>) patients who were negative for mutations in known causative genes, <a href="#2" class="mim-tip-reference" title="Chen, P.-C., Yin, J., Yu, H.-W., Yuan, T., Fernandez, M., Yung, C. K., Trinh, Q. M., Peltekova, V. D., Reid, J. G., Tworog-Dube, E., Morgan, M. B., Muzny, D. M., Stein, L., McPherson, J. D., Roberts, A. E., Gibbs, R. A., Neel, B. G., Kucherlapati, R. &lt;strong&gt;Next-generation sequencing identifies rare variants associated with Noonan syndrome.&lt;/strong&gt; Proc. Nat. Acad. Sci. 111: 11473-11478, 2014.[PubMed: &lt;a href=&quot;https://pubmed.ncbi.nlm.nih.gov/25049390/&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;25049390&lt;/a&gt;] [&lt;a href=&quot;https://doi.org/10.1073/pnas.1324128111&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="25049390">Chen et al. (2014)</a> identified 3 who carried missense mutations in RASA2. Two of the patients had changes in the same codon, tyr326; one mutation was tyr326 to cys (Y326C) and the other was tyr326 to asn (Y326N). The third patient carried an arg511-to-cys (R511C) variant. The patient (NS78) with the Y326C mutation also carried a mutation in RIT1 (F82V; <a href="/entry/609591#0005">609591.0005</a>) known to cause Noonan syndrome-8 (<a href="/entry/615355">615355</a>). No parental DNA was available for segregation analysis. Knockdown studies of RASA2 showed that it plays a role in the RAS-ERK pathway, but no functional testing of these variants was reported. <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=25049390" 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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<strong>REFERENCES</strong>
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<li>
<a id="1" class="mim-anchor"></a>
<a id="Arafeh2015" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Arafeh, R., Qutob, N., Emmanuel, R., Keren-Paz, A., Madore, J., Elkahloun, A., Wilmott, J. S., Gartner, J. J., Di Pizio, A., Winograd-Katz, S., Sindiri, S., Rotkopf, R., and 16 others.
<strong>Recurrent inactivating RASA2 mutations in melanoma.</strong>
Nature Genet. 47: 1408-1410, 2015.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/26502337/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">26502337</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=26502337" 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.3427" target="_blank">Full Text</a>]
</p>
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<a id="2" class="mim-anchor"></a>
<a id="Chen2014" class="mim-anchor"></a>
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<p class="mim-text-font">
Chen, P.-C., Yin, J., Yu, H.-W., Yuan, T., Fernandez, M., Yung, C. K., Trinh, Q. M., Peltekova, V. D., Reid, J. G., Tworog-Dube, E., Morgan, M. B., Muzny, D. M., Stein, L., McPherson, J. D., Roberts, A. E., Gibbs, R. A., Neel, B. G., Kucherlapati, R.
<strong>Next-generation sequencing identifies rare variants associated with Noonan syndrome.</strong>
Proc. Nat. Acad. Sci. 111: 11473-11478, 2014.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/25049390/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">25049390</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=25049390" 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.1324128111" target="_blank">Full Text</a>]
</p>
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<a id="3" class="mim-anchor"></a>
<a id="Gaul1992" class="mim-anchor"></a>
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<p class="mim-text-font">
Gaul, U., Mardon, G., Rubin, G. M.
<strong>A putative Ras GTPase activating protein acts as a negative regulator of signaling by the Sevenless receptor tyrosine kinase.</strong>
Cell 68: 1007-1019, 1992.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/1547500/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">1547500</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=1547500" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1016/0092-8674(92)90073-l" target="_blank">Full Text</a>]
</p>
</div>
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<a id="4" class="mim-anchor"></a>
<a id="Li1996" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Li, S., Satoh, H., Watanabe, T., Nakamura, S., Hattori, S.
<strong>cDNA cloning and chromosomal mapping of a novel human GAP (GAP1M), a GTPase-activating protein of Ras.</strong>
Genomics 35: 625-627, 1996.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/8812506/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">8812506</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=8812506" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1006/geno.1996.0412" target="_blank">Full Text</a>]
</p>
</div>
</li>
<li>
<a id="5" class="mim-anchor"></a>
<a id="Maekawa1994" class="mim-anchor"></a>
<div class="">
<p class="mim-text-font">
Maekawa, M., Li, S., Iwamatsu, A., Morishita, T., Yokota, K., Imai, Y., Kohsaka, S., Nakamura, S., Hattori, S.
<strong>A novel mammalian Ras GTPase-activating protein which has phospholipid-binding and Btk homology regions.</strong>
Molec. Cell. Biol. 14: 6879-6885, 1994.
[PubMed: <a href="https://pubmed.ncbi.nlm.nih.gov/7935405/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">7935405</a>, <a href="https://pubmed.ncbi.nlm.nih.gov/?cmd=link&linkname=pubmed_pubmed&from_uid=7935405" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'PubMed Related', 'domain': 'pubmed.ncbi.nlm.nih.gov'})">related citations</a>]
[<a href="https://doi.org/10.1128/mcb.14.10.6879-6885.1994" target="_blank">Full Text</a>]
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Ada Hamosh - updated : 09/10/2019
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Ada Hamosh - updated : 02/10/2016
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Alan F. Scott : 12/18/1996
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alopez : 09/10/2019
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alopez : 02/10/2016<br>carol : 6/8/2010<br>psherman : 8/12/1999<br>jamie : 1/6/1997<br>jamie : 12/19/1996
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<span class="mim-font">
<strong>*</strong> 601589
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<span class="mim-font">
RAS p21 PROTEIN ACTIVATOR 2; RASA2
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<span class="mim-font">
<em>Alternative titles; symbols</em>
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<span class="mim-font">
GTPase-ACTIVATING PROTEIN OF RAS; GAP1M
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<strong><em>HGNC Approved Gene Symbol: RASA2</em></strong>
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<strong>
<em>
Cytogenetic location: 3q23
&nbsp;
Genomic coordinates <span class="small">(GRCh38)</span> : 3:141,487,027-141,615,344 </span>
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</strong>
<span class="small">(from NCBI)</span>
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<span class="mim-font">
<strong>TEXT</strong>
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<strong>Cloning and Expression</strong>
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<p>Maekawa et al. (1994) isolated a mammalian GTPase-activating protein of RAS from rat (GAP1M) that shows sequence similarity to the suppressor of RAS (see 190020) function in Drosophila, known as Gap1 (Gaul et al., 1992). Expression was relatively high in brain, placenta, and kidney but lower in other tissues. A recombinantly expressed protein containing the GAP-related domain was shown to stimulate GTPase activity of RAS. </p><p>Li et al. (1996) isolated the human homolog of rat GAP1M from a brain cDNA library. The deduced 853-amino acid protein is 89.4% identical to the rat protein. </p>
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<span class="mim-font">
<strong>Mapping</strong>
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<p>Using a panel of somatic cell hybrid DNAs, Li et al. (1996) mapped the human GAP1M gene to chromosome 3. By fluorescence in situ hybridization, they mapped GAP1M to chromosome 3q22-q23. </p>
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<h4>
<span class="mim-font">
<strong>Molecular Genetics</strong>
</span>
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<span class="mim-text-font">
<p><strong><em>Somatic Mutation</em></strong></p><p>
Arafeh et al. (2015) analyzed 501 melanoma (see 155600) exomes and found that RASA2 was mutated in 5% of melanomas. Recurrent loss-of-function mutations in RASA2 were found to increase RAS activation and melanoma cell growth and migration. RASA2 expression was lost in at least 30% of human melanomas analyzed and was associated with reduced patient survival. </p><p><strong><em>Associations Pending Confirmation</em></strong></p><p>
Among 27 Noonan syndrome (see 163950) patients who were negative for mutations in known causative genes, Chen et al. (2014) identified 3 who carried missense mutations in RASA2. Two of the patients had changes in the same codon, tyr326; one mutation was tyr326 to cys (Y326C) and the other was tyr326 to asn (Y326N). The third patient carried an arg511-to-cys (R511C) variant. The patient (NS78) with the Y326C mutation also carried a mutation in RIT1 (F82V; 609591.0005) known to cause Noonan syndrome-8 (615355). No parental DNA was available for segregation analysis. Knockdown studies of RASA2 showed that it plays a role in the RAS-ERK pathway, but no functional testing of these variants was reported. </p>
</span>
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</div>
</div>
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<h4>
<span class="mim-font">
<strong>REFERENCES</strong>
</span>
</h4>
<div>
<p />
</div>
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<li>
<p class="mim-text-font">
Arafeh, R., Qutob, N., Emmanuel, R., Keren-Paz, A., Madore, J., Elkahloun, A., Wilmott, J. S., Gartner, J. J., Di Pizio, A., Winograd-Katz, S., Sindiri, S., Rotkopf, R., and 16 others.
<strong>Recurrent inactivating RASA2 mutations in melanoma.</strong>
Nature Genet. 47: 1408-1410, 2015.
[PubMed: 26502337]
[Full Text: https://doi.org/10.1038/ng.3427]
</p>
</li>
<li>
<p class="mim-text-font">
Chen, P.-C., Yin, J., Yu, H.-W., Yuan, T., Fernandez, M., Yung, C. K., Trinh, Q. M., Peltekova, V. D., Reid, J. G., Tworog-Dube, E., Morgan, M. B., Muzny, D. M., Stein, L., McPherson, J. D., Roberts, A. E., Gibbs, R. A., Neel, B. G., Kucherlapati, R.
<strong>Next-generation sequencing identifies rare variants associated with Noonan syndrome.</strong>
Proc. Nat. Acad. Sci. 111: 11473-11478, 2014.
[PubMed: 25049390]
[Full Text: https://doi.org/10.1073/pnas.1324128111]
</p>
</li>
<li>
<p class="mim-text-font">
Gaul, U., Mardon, G., Rubin, G. M.
<strong>A putative Ras GTPase activating protein acts as a negative regulator of signaling by the Sevenless receptor tyrosine kinase.</strong>
Cell 68: 1007-1019, 1992.
[PubMed: 1547500]
[Full Text: https://doi.org/10.1016/0092-8674(92)90073-l]
</p>
</li>
<li>
<p class="mim-text-font">
Li, S., Satoh, H., Watanabe, T., Nakamura, S., Hattori, S.
<strong>cDNA cloning and chromosomal mapping of a novel human GAP (GAP1M), a GTPase-activating protein of Ras.</strong>
Genomics 35: 625-627, 1996.
[PubMed: 8812506]
[Full Text: https://doi.org/10.1006/geno.1996.0412]
</p>
</li>
<li>
<p class="mim-text-font">
Maekawa, M., Li, S., Iwamatsu, A., Morishita, T., Yokota, K., Imai, Y., Kohsaka, S., Nakamura, S., Hattori, S.
<strong>A novel mammalian Ras GTPase-activating protein which has phospholipid-binding and Btk homology regions.</strong>
Molec. Cell. Biol. 14: 6879-6885, 1994.
[PubMed: 7935405]
[Full Text: https://doi.org/10.1128/mcb.14.10.6879-6885.1994]
</p>
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Ada Hamosh - updated : 09/10/2019<br>Ada Hamosh - updated : 02/10/2016
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Creation Date:
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Alan F. Scott : 12/18/1996
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