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1:
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<a href="/entry/113705?search=113705%20114480%20600185%20604370%20612555%20613347%20614320&highlight=113705%2C114480%2C600185%2C604370%2C612555%2C613347%2C614320">
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113705.
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BRCA1 DNA REPAIR-ASSOCIATED PROTEIN; BRCA1
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Cytogenetic location:
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<a href="/geneMap/17/610?start=-3&limit=10&highlight=610">
17q21.31</a></span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font"><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr17:43044295-43170327&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'})">17:43,044,295-43,170,327</a></span>
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Location
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Phenotype
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Phenotype <br /> MIM number
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Inheritance
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<a href="/geneMap/17/610?start=-3&limit=10&highlight=610">
17q21.31
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{Breast-ovarian cancer, familial, 1}
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<a href="/entry/604370"> 604370 </a>
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<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Multifactorial">Mu</abbr>
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<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
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{Pancreatic cancer, susceptibility to, 4}
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<a href="/entry/614320"> 614320 </a>
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</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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Fanconi anemia, complementation group S
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<span class="mim-font">
<a href="/entry/617883"> 617883 </a>
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<abbr class="mim-tip-hint" title="Autosomal recessive">AR</abbr>
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<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="3 - The molecular basis of the disorder is known"> 3 </abbr>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimGeneMapFold_1" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimLinksFold_1" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=113705[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></dd>
</dl>
</td>
<td>
<dl>
<dt>Genome</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Location/View?db=core;g=ENSG00000012048;t=ENST00000357654" class="mim-tip-hint" title="Genome databases for vertebrates and other eukaryotic species." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/genome/gdv/browser/gene/?id=672" class="mim-tip-hint" title="Detailed views of the complete genomes of selected organisms from vertebrates to protozoa." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Genome Viewer', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Genome Viewer</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=113705" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>DNA</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Transcript/Sequence_cDNA?db=core;g=ENSG00000012048;t=ENST00000357654" class="mim-tip-hint" title="Transcript-based views for coding and noncoding DNA." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl (MANE Select)</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_001407571,NM_001407581,NM_001407582,NM_001407583,NM_001407585,NM_001407587,NM_001407590,NM_001407591,NM_001407593,NM_001407594,NM_001407596,NM_001407597,NM_001407598,NM_001407602,NM_001407603,NM_001407605,NM_001407610,NM_001407611,NM_001407612,NM_001407613,NM_001407614,NM_001407615,NM_001407616,NM_001407617,NM_001407618,NM_001407619,NM_001407620,NM_001407621,NM_001407622,NM_001407623,NM_001407624,NM_001407625,NM_001407626,NM_001407627,NM_001407628,NM_001407629,NM_001407630,NM_001407631,NM_001407632,NM_001407633,NM_001407634,NM_001407635,NM_001407636,NM_001407637,NM_001407638,NM_001407639,NM_001407640,NM_001407641,NM_001407642,NM_001407644,NM_001407645,NM_001407646,NM_001407647,NM_001407648,NM_001407649,NM_001407652,NM_001407653,NM_001407654,NM_001407655,NM_001407656,NM_001407657,NM_001407658,NM_001407659,NM_001407660,NM_001407661,NM_001407662,NM_001407663,NM_001407664,NM_001407665,NM_001407666,NM_001407667,NM_001407668,NM_001407669,NM_001407670,NM_001407671,NM_001407672,NM_001407673,NM_001407674,NM_001407675,NM_001407676,NM_001407677,NM_001407678,NM_001407679,NM_001407680,NM_001407681,NM_001407682,NM_001407683,NM_001407684,NM_001407685,NM_001407686,NM_001407687,NM_001407688,NM_001407689,NM_001407690,NM_001407691,NM_001407692,NM_001407694,NM_001407695,NM_001407696,NM_001407697,NM_001407698,NM_001407724,NM_001407725,NM_001407726,NM_001407727,NM_001407728,NM_001407729,NM_001407730,NM_001407731,NM_001407732,NM_001407733,NM_001407734,NM_001407735,NM_001407736,NM_001407737,NM_001407738,NM_001407739,NM_001407740,NM_001407741,NM_001407742,NM_001407743,NM_001407744,NM_001407745,NM_001407746,NM_001407747,NM_001407748,NM_001407749,NM_001407750,NM_001407751,NM_001407752,NM_001407838,NM_001407839,NM_001407841,NM_001407842,NM_001407843,NM_001407844,NM_001407845,NM_001407846,NM_001407847,NM_001407848,NM_001407849,NM_001407850,NM_001407851,NM_001407852,NM_001407853,NM_001407854,NM_001407858,NM_001407859,NM_001407860,NM_001407861,NM_001407862,NM_001407863,NM_001407874,NM_001407875,NM_001407879,NM_001407881,NM_001407882,NM_001407884,NM_001407885,NM_001407886,NM_001407887,NM_001407889,NM_001407894,NM_001407895,NM_001407896,NM_001407897,NM_001407898,NM_001407899,NM_001407900,NM_001407902,NM_001407904,NM_001407906,NM_001407907,NM_001407908,NM_001407909,NM_001407910,NM_001407915,NM_001407916,NM_001407917,NM_001407918,NM_001407919,NM_001407920,NM_001407921,NM_001407922,NM_001407923,NM_001407924,NM_001407925,NM_001407926,NM_001407927,NM_001407928,NM_001407929,NM_001407930,NM_001407931,NM_001407932,NM_001407933,NM_001407934,NM_001407935,NM_001407936,NM_001407937,NM_001407938,NM_001407939,NM_001407940,NM_001407941,NM_001407942,NM_001407943,NM_001407944,NM_001407945,NM_001407946,NM_001407947,NM_001407948,NM_001407949,NM_001407950,NM_001407951,NM_001407952,NM_001407953,NM_001407954,NM_001407955,NM_001407956,NM_001407957,NM_001407958,NM_001407959,NM_001407960,NM_001407962,NM_001407963,NM_001407964,NM_001407965,NM_001407966,NM_001407967,NM_001407968,NM_001407969,NM_001407970,NM_001407971,NM_001407972,NM_001407973,NM_001407974,NM_001407975,NM_001407976,NM_001407977,NM_001407978,NM_001407979,NM_001407980,NM_001407981,NM_001407982,NM_001407983,NM_001407984,NM_001407985,NM_001407986,NM_001407990,NM_001407991,NM_001407992,NM_001407993,NM_001408392,NM_001408396,NM_001408397,NM_001408398,NM_001408399,NM_001408400,NM_001408401,NM_001408402,NM_001408403,NM_001408404,NM_001408406,NM_001408407,NM_001408408,NM_001408409,NM_001408410,NM_001408411,NM_001408412,NM_001408413,NM_001408414,NM_001408415,NM_001408416,NM_001408418,NM_001408419,NM_001408420,NM_001408421,NM_001408422,NM_001408423,NM_001408424,NM_001408425,NM_001408426,NM_001408427,NM_001408428,NM_001408429,NM_001408430,NM_001408431,NM_001408432,NM_001408433,NM_001408434,NM_001408435,NM_001408436,NM_001408437,NM_001408438,NM_001408439,NM_001408440,NM_001408441,NM_001408442,NM_001408443,NM_001408444,NM_001408445,NM_001408446,NM_001408447,NM_001408448,NM_001408450,NM_001408451,NM_001408452,NM_001408453,NM_001408454,NM_001408455,NM_001408456,NM_001408457,NM_001408458,NM_001408459,NM_001408460,NM_001408461,NM_001408462,NM_001408463,NM_001408464,NM_001408465,NM_001408466,NM_001408467,NM_001408468,NM_001408469,NM_001408470,NM_001408472,NM_001408473,NM_001408474,NM_001408475,NM_001408476,NM_001408478,NM_001408479,NM_001408480,NM_001408481,NM_001408482,NM_001408483,NM_001408484,NM_001408485,NM_001408489,NM_001408490,NM_001408491,NM_001408492,NM_001408493,NM_001408494,NM_001408495,NM_001408496,NM_001408497,NM_001408498,NM_001408499,NM_001408500,NM_001408501,NM_001408502,NM_001408503,NM_001408504,NM_001408505,NM_001408506,NM_001408507,NM_001408508,NM_001408509,NM_001408510,NM_001408511,NM_001408512,NM_001408513,NM_001408514,NM_007294,NM_007297,NM_007298,NM_007299,NM_007300" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_007294" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq (MANE)', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq (MANE Select)</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=113705" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Protein</dt>
<dd><a href="https://hprd.org/summary?hprd_id=00218&isoform_id=00218_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></dd>
<dd><a href="https://www.proteinatlas.org/search/BRCA1" 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></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/protein/555932,728984,1000569,1498737,1546074,1698399,1841427,2218154,6552299,9739179,23266700,24430095,24430097,24430099,24430101,24430104,24430106,24430108,24430110,24430112,24431185,24431187,24431189,25140446,30039659,32140995,37537746,38382815,47939870,52001522,52001524,52001526,53794093,55250220,70611296,70959462,73665398,73665400,73665402,73665404,73665406,75874527,75874617,75874675,75874794,75874871,75874961,75875069,75875129,78070589,78070810,82623248,82623250,82623252,82623254,82623256,82623258,82623262,82623271,82623276,82623285,82623287,82623289,82623291,82623293,82623295,82623297,82623299,82623301,82623303,82623305,82623307,82623309,82623311,82623313,82623315,82623317,82623319,84626582,84626584,86279115,92096024,94315232,116283824,119581326,119581327,119581328,119581329,119581330,119581331,119581332,119581333,119581334,119581335,119581336,119581337,119581338,119581339,119581340,119581341,119581342,119581343,119581344,119581345,119581346,221045788,237681119,237681121,237681123,237681125,237930356,344179065,350540199,350540201,350540203,350540205,350540207,350540209,350540211,353441749,408773036,408773038,408773040,408773042,408773044,408773046,408773048,408773050,655204045,655204048,655204051,655204056,655204086,655204131,655204145,655204176,655204185,655204200,655204214,655204234,655204246,655204252,655204270,655204290,655204304,655204315,655204331,655204348,655204685,655204701,655204741,655204766,655204773,655204781,655204824,655204872,655204873,655204916,655204955,655205017,725825441,815932479,815932481,815932483,815932485,815932487,815932489,815932491,815932493,819326628,819327290,819327325,819327355,819327357,827494114,827514371,891070991,891071011,891071029,896689375,896689377,925719367,929982561,952951593,952951595,952951597,974031366,974031368,1003107961,1003107963,1003107965,1003107967,1003107969,1003107971,1003107973,1003107975,1003107977,1003107979,1060746688,1246291365,1367361247,1378096911,1378096913,1378096915,1378096917,1378096919,1378096921,1378096923,1378096925,1378096927,1378096929,1378096931,1378096933,1378096935,1378096937,1378096939,1435082957,1435082959,1435082961,1435082963,1435082965,1435082967,1435082969,1435082971,1483525253,1483525255,1483525257,1483525259,1483525260,1483525262,1483525264,1483525275,1483525277,1483525282,1483525284,1483525286,1483525288,1483525290,1483525292,1483525294,1483525296,1483525298,1483525300,1483525302,1483525304,1483525306,1483525308,1483525310,1483525312,1483525314,1483525316,1483525318,1483525320,1483525322,1483525324,1483525326,1483976470,1483976472,1483976474,1534889324,1534889326,1534889328,1534889330,1534889332,1534889334,1534889336,1534889338,1534889340,1534889342,1534889344,1534889346,1534889348,1534889350,1534889352,1534889354,1534889356,1534889358,1534889360,1534889362,1534889364,1534889366,1534889368,1534889370,1534889372,1534889374,1534889376,1534889378,1534889380,1534889382,1534889384,1534889386,1534889388,1534889390,1534889392,1534889394,1534889396,1534889398,1534889400,1534889402,1534889404,1534889406,1534889408,1534889410,1534889412,1534889414,1534889416,1534889418,1534889420,1534889422,1534889424,1534889426,1534889428,1534889430,1534889432,1534889434,1534889436,1534889438,1534889440,1534889442,1534889445,1591645911,1591645913,1591645915,1591645917,1591645919,1591645921,1591645923,1591645925,1591645927,1591645929,1591645931,1591645933,1591645935,1591645937,1591645939,1591645941,1591645943,1591645945,1591645947,1591645949,1591645951,1591645953,1591645955,1591645957,1591645959,1591645961,1591645963,1591645965,1591645967,1591645969,1591645971,1591645973,1591645975,1591645977,1591645979,1591645981,1591645983,1591645985,1591645987,1591645989,1591645991,1591645993,1591645995,1591645997,1591645999,1591646001,1591646003,1591646005,1591646007,1591646009,1591646011,1591646013,1591646015,1591646017,1591646019,1591646021,1591646023,1591646025,1591646027,1591646029,1591646031,1591646033,1591646035,1591646037,1591646039,1591646041,1591646043,1591646045,1591646047,1591646049,1591646051,1591646053,1591646055,1591646057,1591646059,1591646061,1591646063,1591646065,1591646067,1591646069,1591646071,1591646073,1591646075,1591646077,1591646079,1591646081,1591646083,1591646085,1591646087,1591646089,1591646091,1591646093,1591646095,1591646097,1591646101,1591646107,1591646111,1591646113,1591646115,1591646119,1591646121,1591646123,1591646125,1591646129,1591646131,1591646133,1591646135,1591646137,1591646139,1591646141,1591646143,1591646145,1591646147,1591646149,1591646151,1591646153,1591646155,1591646157,1591646159,1591646161,1591646163,1591646165,1591646167,1591646169,1591646171,1591646173,1591646175,1591646177,1591646179,1591646181,1591646183,1591646185,1591646187,1591646189,1591646191,1591646193,1591646195,1591646197,1591646199,1591646201,1591646203,1591646205,1591646207,1591646209,1591646211,1591646213,1591646215,1591646217,1591646219,1591646221,1591646223,1591646225,1591646227,1591646229,1591646231,1591646233,1591646235,1591646237,1591646239,1591646241,1591646245,1591646247,1591646249,1591646251,1591646253,1591646255,1591646257,1591646259,1591646261,1591646263,1591646265,1591646269,1591646271,1591646273,1591646277,1591646279,1591646285,1591646289,1591646291,1591646293,1591646295,1591646297,1591646299,1591646301,1591646303,1591646305,1591646307,1591646309,1591646311,1591646313,1591646315,1591646317,1591646319,1591646321,1591646323,1591646325,1591646327,1591646331,1591646337,1591646339,1591646341,1591646343,1591646345,1591646347,1591646349,1591646351,1591646353,1591646355,1591646357,1591646359,1591646361,1591646363,1591646365,1591646367,1591646369,1591646373,1591646375,1591646377,1591646379,1591646381,1591646383,1591646385,1591646387,1591646389,1591646391,1591646393,1591646395,1591646397,1591646399,1591646401,1591646403,1591646405,1591646407,1591646409,1591646411,1591646413,1591646415,1591646417,1591646419,1591646421,1591646423,1591646425,1591646427,1591646429,1591646431,1591646433,1591646435,1591646437,1591646439,1591646441,1591646443,1591646445,1591646447,1591646449,1591646451,1633439648,1633439650,1633439661,1775113870,1775113872,1811001076,1821655611,1821655613,1821655615,1821655621,1896049792,1896049794,1896049796,1931625759,2001549011,2029084593,2029084595,2029084597,2029084599,2043420397,2043420465,2043420467,2043420469,2043420471,2043420538,2043420540,2043420542,2043420544,2054258294,2054258296,2094552264,2094552272,2095878425,2164862743,2164862749,2164862751,2164862757,2164862765,2164862781,2164862783,2164862785,2164862787,2164862789,2164862791,2164862793,2164862795,2164862797,2164862799,2164862801,2164862803,2178104996,2178104998,2178105000,2178105002,2178105203,2178105575,2179160378,2214793706,2218468102,2218468124,2218469276,2218469280,2218469282,2218469284,2248537882,2249006927,2249006935,2249006949,2249006951,2249006953,2249006955,2249006961,2249006973,2249006975,2249006977,2249006989,2249006991,2249006993,2249006998,2249007000,2249007002,2249007004,2249007008,2249007012,2249007021,2249007023,2249007027,2249007031,2249007033,2249007035,2249007039,2249007045,2249007047,2249007051,2249007058,2249007060,2249007068,2249007070,2249007072,2249007074,2249007076,2249007078,2249007080,2249007091,2249007093,2249007106,2249007124,2249007127,2249007129,2249007131,2249007133,2249007138,2249007144,2249007146,2249007149,2249007153,2249007155,2249007158,2249218165,2249629730,2249629735,2249629737,2249629741,2249629743,2249629754,2249629756,2249629758,2249629760,2249629762,2249629769,2249629771,2249629773,2249629775,2249629777,2249629787,2249629789,2249629791,2249629793,2249629799,2249629801,2249629803,2249629805,2249629807,2249629809,2249629813,2249629819,2249629821,2249629823,2249629825,2249629829,2249629833,2249629840,2249629844,2249629848,2249629852,2249629854,2249629862,2249629864,2249629870,2249629872,2249629876,2249629879,2249629885,2249629887,2249629889,2249629891,2249629895,2249629897,2249629909,2249629917,2249629919,2249629929,2249629931,2249629937,2249629945,2249629950,2249629952,2249629954,2249629958,2249629960,2249629962,2249629966,2249629975,2249629977,2249629981,2249629983,2249629987,2249629989,2249629991,2249629993,2249629997,2249629999,2249630003,2249630011,2250017139,2250017141,2250017151,2250017165,2250017167,2250017187,2250017189,2250017197,2250017202,2250017206,2250017224,2250017250,2250017256,2250017260,2250017272,2250017274,2250017276,2250017278,2250017282,2250017290,2250017298,2250017304,2250017306,2250017308,2250017329,2250017337,2250017339,2250017345,2250017347,2250017349,2250017351,2250017353,2250017355,2250017362,2250017366,2250017368,2250017381,2250017383,2250017389,2250017393,2250017405,2250017411,2250017413,2250017417,2250017419,2250232291,2250232293,2250232295,2250232302,2250232314,2250232316,2250232320,2250232322,2250232324,2250232332,2250232334,2250232336,2250232340,2250232342,2250232345,2250232347,2250232349,2250232355,2250232357,2250232366,2250232368,2250232372,2250232374,2250232378,2250232380,2250232388,2250232394,2250232400,2250232408,2250232410,2250232412,2250232414,2250232416,2250232418,2250232426,2250232432,2250232434,2250232441,2250232444,2250232448,2250232453,2250232458,2250232460,2250232462,2250232467,2250232472,2250232476,2250232480,2250232482,2250232484,2250232489,2250232491,2250232496,2250232498,2250232502,2250232504,2250232508,2250232510,2250232512,2250232520,2250232527,2250232529,2250232531,2250232536,2250232539,2250232541,2250232547,2250232551,2250232553,2250232555,2250232557,2250232559,2250232562,2250232575,2250232577,2250232581,2255444081,2255444083,2255444085,2255444087,2255444091,2255444093,2255444095,2255444097,2255444101,2255444107,2255444112,2255444118,2255444122,2255444126,2255444135,2255444139,2255444145,2255444147,2255444151,2255444153,2255444157,2255444159,2255444163,2255444167,2255444169,2255444174,2255444176,2255444178,2255444180,2255444184,2255444192,2255444194,2255444196,2255444200,2255444202,2255444204,2255444206,2255444208,2255444212,2255444216,2255444218,2255444220,2255444222,2255444224,2255444228,2255444232,2255444241,2255444249,2255444251,2255444253,2255444257,2255444259,2255444261,2255444263,2255444265,2255444267,2255444275,2255444282,2255444288,2255444306,2255444308,2255444312,2255444318,2255444320,2255444324,2255444344,2255444346,2255444573,2255444941,2255445265,2255445399,2255445557,2255446218,2255446601,2255446638,2255446641,2255446662,2255446667,2255446697,2255446717,2255447520,2255447721,2255447825,2255448079,2255448093,2255448600,2255448770,2255449024,2255449180,2255449844,2255450433,2255450585,2255450762,2255451067,2255451245,2255451431,2255451928,2255452079,2255452260,2255452523,2255452864,2255453230,2255453587,2255453951,2255454031,2255454272,2255454491,2255454693,2255455096,2255455874,2255456066,2255456860,2389772339,2389772341,2389772343,2389772345,2389772347,2389772349,2389772351,2396616248,2396616250,2396616252,2396616370,2430144117,2430144119,2430144121,2430144123,2430144125,2430144127,2430144129,2430144131,2430144133,2430144135,2450748324,2450748325,2450748326,2450748327,2450748328,2468371728,2468371792,2468371861,2468371888,2468371927,2468371966,2468372051,2468372089,2468372140,2468372185,2468372302,2468372349,2468372391,2468372427,2468372461,2468372497,2468372629,2468372656,2468372732,2468372756,2468372816,2468372848,2468372873,2468372900,2468372952,2468372976,2468373004,2468373025,2468373061,2468373086,2468373110,2468373155,2468373213,2468373236,2468373259,2468373377,2468373407,2557734826,2557734828,2557734830,2557734832,2557734834,2557734836,2607637241,2607637243,2607637245,2607637247,2616260797,2616260799,2616260801,2616260803,2616260805,2701656703,2703623452,2703623454,2703623456,2703623458,2909903171,2909903173" 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></dd>
<dd><a href="https://www.uniprot.org/uniprotkb/P38398" 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></dd>
</dl>
</td>
<td>
<dl>
<dt>Gene Info</dt>
<dd><a href="http://biogps.org/#goto=genereport&id=672" 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></dd>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=ENSG00000012048;t=ENST00000357654" 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></dd>
<dd><a href="https://www.genecards.org/cgi-bin/carddisp.pl?gene=BRCA1" 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></dd>
<dd><a href="http://amigo.geneontology.org/amigo/search/annotation?q=BRCA1" 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></dd>
<dd><a href="https://www.genome.jp/dbget-bin/www_bget?hsa+672" 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></dd>
<dd><a href="http://v1.marrvel.org/search/gene/BRCA1" 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:672" class="mim-tip-hint" title="Monarch Initiative." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Monarch', 'domain': 'monarchinitiative.org'})">Monarch</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/672" class="mim-tip-hint" title="Gene-specific map, sequence, expression, structure, function, citation, and homology data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Gene', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Gene</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgGene?db=hg38&hgg_chrom=chr17&hgg_gene=ENST00000357654.9&hgg_start=43044295&hgg_end=43170327&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></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://search.clinicalgenome.org/kb/gene-dosage/HGNC:1100" class="mim-tip-hint" title="A ClinGen curated resource of genes and regions of the genome that are dosage sensitive and should be targeted on a cytogenomic array." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinGen Dosage', 'domain': 'dosage.clinicalgenome.org'})">ClinGen Dosage</a></dd>
<dd><a href="https://search.clinicalgenome.org/kb/genes/HGNC:1100" 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></dd>
<dd><a href="https://medlineplus.gov/genetics/gene/brca1" class="mim-tip-hint" title="Consumer-friendly information about the effects of genetic variation on human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MedlinePlus Genetics', 'domain': 'medlineplus.gov'})">MedlinePlus Genetics</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=113705[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></dd>
</dl>
</td>
<td>
<dl>
<dt>Variation</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/clinvar?term=113705[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></dd>
<dd><a href="https://www.deciphergenomics.org/gene/BRCA1/overview/clinical-info" class="mim-tip-hint" title="DECIPHER" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'DECIPHER', 'domain': 'DECIPHER'})">DECIPHER</a></dd>
<dd><a href="https://gnomad.broadinstitute.org/gene/ENSG00000012048" 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></dd>
<dd><a href="https://www.ebi.ac.uk/gwas/search?query=BRCA1" 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 </a></dd>
<dd><a href="https://www.gwascentral.org/search?q=BRCA1" 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 </a></dd>
<dd><a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=BRCA1" class="mim-tip-hint" title="Human Gene Mutation Database; published mutations causing or associated with human inherited disease; disease-associated/functional polymorphisms." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HGMD', 'domain': 'hgmd.cf.ac.uk'})">HGMD</a></dd>
<dd>Locus Specific DBs</dd>
<dd style="margin-left: 0.5em;"><a href="http://chromium.liacs.nl/LOVD2/cancer/home.php?select_db=BRCA1" title="LOVD - BReast CAncer 1 - literature unclassified variants (BRCA1)" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">LOVD - BReast CAncer 1 - l…</a></dd><dd style="margin-left: 0.5em;"><a href="http://databases.lovd.nl/genomed/home.php?select_db=BRCA1" title="Zhejiang University-Adinovo Center BRCA1 Database" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">Zhejiang University-Adinov…</a></dd><dd style="margin-left: 0.5em;"><a href="http://research.nhgri.nih.gov/bic/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">Breast Cancer</a></dd><dd style="margin-left: 0.5em;"><a href="http://www.umd.be/BRCA1/" title="The UMD BRCA1 mutations database" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">The UMD BRCA1 mutations da…</a></dd>
<dd><a href="https://evs.gs.washington.edu/EVS/PopStatsServlet?searchBy=Gene+Hugo&target=BRCA1&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></dd>
<dd><a href="https://www.pharmgkb.org/gene/PA25411" 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></dd>
</dl>
</td>
<td>
<dl>
<dt>Animal Models</dt>
<dd><a href="https://www.alliancegenome.org/gene/HGNC:1100" 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></dd>
<dd><a href="https://www.mousephenotype.org/data/genes/MGI:104537" class="mim-tip-hint" title="International Mouse Phenotyping Consortium." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'IMPC', 'domain': 'knockoutmouse.org'})">IMPC</a></dd>
<dd><a href="http://v1.marrvel.org/search/gene/BRCA1#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></dd>
<dd><a href="http://www.informatics.jax.org/marker/MGI:104537" 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></dd>
<dd><a href="https://www.mmrrc.org/catalog/StrainCatalogSearchForm.php?search_query=MGI:104537" class="mim-tip-hint" title="Mutant Mouse Resource & Research Centers." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MMRRC', 'domain': 'mmrrc.org'})">MMRRC</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/672/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></dd>
<dd><a href="https://www.orthodb.org/?ncbi=672" class="mim-tip-hint" title="Hierarchical catalogue of orthologs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrthoDB', 'domain': 'orthodb.org'})">OrthoDB</a></dd>
<dd><a href="https://wormbase.org/db/gene/gene?name=WBGene00000264;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></dd> Wormbase Gene
</dl>
</td>
<td>
<dl>
<dt>Cell Lines</dt>
<dd><a href="https://catalog.coriell.org/Search?q=OmimNum:113705" class="definition" title="Coriell Cell Repositories; cell cultures and DNA derived from cell cultures." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'CCR', 'domain': 'ccr.coriell.org'})">Coriell</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Cellular Pathways</dt>
<dd><a href="https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+hsa:672" 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></dd>
<dd><a href="https://reactome.org/content/query?q=BRCA1&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></dd>
</dl>
</td>
</tr>
</tbody>
</table>
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<a href="#mimLinksFold_1" data-toggle="collapse">▲ Close</a>
</div>
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</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
2:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/114480?search=113705%20114480%20600185%20604370%20612555%20613347%20614320&highlight=113705%2C114480%2C600185%2C604370%2C612555%2C613347%2C614320">
<span class="mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
114480.
</span>
BREAST CANCER
</a>
</span>
<br />
<span class="mim-font">BREAST CANCER, FAMILIAL MALE, INCLUDED</span>
<br />
<span class="text-muted">
Cytogenetic locations:
<span class="mim-font">
<a href="/geneMap/1/567?start=-3&limit=10&highlight=567">
1p34.1</a></span>,
<span class="mim-font">
<a href="/geneMap/2/914?start=-3&limit=10&highlight=914">
2q33.1</a></span>,
<span class="mim-font">
<a href="/geneMap/2/982?start=-3&limit=10&highlight=982">
2q35</a></span>,
<span class="mim-font">
<a href="/geneMap/3/876?start=-3&limit=10&highlight=876">
3q26.32</a></span>,
<span class="mim-font">
<a href="/geneMap/5/739?start=-3&limit=10&highlight=739">
5q34</a></span>,
<span class="mim-font">
<a href="/geneMap/6/19?start=-3&limit=10&highlight=19">
6p25.2</a></span>,
<span class="mim-font">
<a href="/geneMap/6/962?start=-3&limit=10&highlight=962">
6q25.1-q25.2</a></span>,
<span class="mim-font">
<a href="/geneMap/8/263?start=-3&limit=10&highlight=263">
8q11.23</a></span>,
<span class="mim-font">
<a href="/geneMap/11/88?start=-3&limit=10&highlight=88">
11p15.4</a></span>,
<span class="mim-font">
<a href="/geneMap/11/897?start=-3&limit=10&highlight=897">
11q22.3</a></span>,
<span class="mim-font">
<a href="/geneMap/12/240?start=-3&limit=10&highlight=240">
12p12.1</a></span>,
<span class="mim-font">
<a href="/geneMap/13/83?start=-3&limit=10&highlight=83">
13q13.1</a></span>,
<span class="mim-font">
<a href="/geneMap/14/580?start=-3&limit=10&highlight=580">
14q32.33</a></span>,
<span class="mim-font">
<a href="/geneMap/14/593?start=-3&limit=10&highlight=593">
14q32.33</a></span>,
<span class="mim-font">
<a href="/geneMap/15/103?start=-3&limit=10&highlight=103">
15q15.1</a></span>,
<span class="mim-font">
<a href="/geneMap/16/582?start=-3&limit=10&highlight=582">
16q22.1</a></span>,
<span class="mim-font">
<a href="/geneMap/17/175?start=-3&limit=10&highlight=175">
17p13.1</a></span>,
<span class="mim-font">
<a href="/geneMap/17/720?start=-3&limit=10&highlight=720">
17q21.33</a></span>,
<span class="mim-font">
<a href="/geneMap/17/819?start=-3&limit=10&highlight=819">
17q23.2</a></span>,
<span class="mim-font">
<a href="/geneMap/17/824?start=-3&limit=10&highlight=824">
17q23.2</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">114480</span></span>
<br />
<a href="#mimPhenotypeMapFold_2" id="mimPhenotypeMapToggle_2" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimPhenotypeMapToggleTriangle_2" class="mimPingletonToggleTriangle" style="color: DarkOrchid">►</span> Phenotype-Gene Relationships</span></a>
<a href="#mimDisorderCodesFold_2" id="mimDisorderCodesToggle_2" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_2" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_2" id="mimLinksToggle_2" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_2" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimPhenotypeMapFold_2" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Phenotype-Gene Relationships
</caption>
<thead>
<tr>
<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/1/567?start=-3&limit=10&highlight=567">
1p34.1
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, invasive ductal}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
RAD54L
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/603615"> 603615 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/914?start=-3&limit=10&highlight=914">
2q33.1
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, protection against}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
CASP8
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601763"> 601763 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/2/982?start=-3&limit=10&highlight=982">
2q35
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
BARD1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/601593"> 601593 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/3/876?start=-3&limit=10&highlight=876">
3q26.32
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
PIK3CA
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/171834"> 171834 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/5/739?start=-3&limit=10&highlight=739">
5q34
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
HMMR
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600936"> 600936 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/19?start=-3&limit=10&highlight=19">
6p25.2
</a>
</span>
</td>
<td>
<span class="mim-font">
{?Breast cancer susceptibility}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</abbr>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="1 - The disorder is placed on the map due to its association with a gene, but the underlying defect is not known"> 1 </abbr>
</span>
</td>
<td>
<span class="mim-font">
NQO2
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/160998"> 160998 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/6/962?start=-3&limit=10&highlight=962">
6q25.1-q25.2
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
ESR1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/133430"> 133430 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/8/263?start=-3&limit=10&highlight=263">
8q11.23
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
RB1CC1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/606837"> 606837 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/88?start=-3&limit=10&highlight=88">
11p15.4
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
SLC22A1L
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602631"> 602631 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/11/897?start=-3&limit=10&highlight=897">
11q22.3
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
ATM
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/607585"> 607585 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/12/240?start=-3&limit=10&highlight=240">
12p12.1
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
KRAS
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/190070"> 190070 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/13/83?start=-3&limit=10&highlight=83">
13q13.1
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, male, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
BRCA2
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600185"> 600185 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/580?start=-3&limit=10&highlight=580">
14q32.33
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
XRCC3
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600675"> 600675 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/14/593?start=-3&limit=10&highlight=593">
14q32.33
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
AKT1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/164730"> 164730 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/15/103?start=-3&limit=10&highlight=103">
15q15.1
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
RAD51
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/179617"> 179617 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/582?start=-3&limit=10&highlight=582">
16q22.1
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, lobular, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
CDH1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/192090"> 192090 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/175?start=-3&limit=10&highlight=175">
17p13.1
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
TP53
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/191170"> 191170 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/720?start=-3&limit=10&highlight=720">
17q21.33
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
PHB1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/176705"> 176705 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/819?start=-3&limit=10&highlight=819">
17q23.2
</a>
</span>
</td>
<td>
<span class="mim-font">
Breast cancer, somatic
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </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">
PPM1D
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605100"> 605100 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/824?start=-3&limit=10&highlight=824">
17q23.2
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, early-onset, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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">
BRIP1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605882"> 605882 </a>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimPhenotypeMapFold_2" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimLinksFold_2" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=114480[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></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=19054&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://clinicaltrials.gov/search?cond=BREAST CANCER" class="mim-tip-hint" title="A registry of federally and privately supported clinical trials conducted in the United States and around the world." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=19054&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/books/NBK1247/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></dd>
<dd><a href="https://www.diseaseinfosearch.org/x/8375" 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></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=114480[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></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=227535" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Animal Models</dt>
<dd><a href="https://www.alliancegenome.org/disease/DOID:1612" 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></dd>
<dd><a href="http://www.informatics.jax.org/disease/114480" 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></dd>
<dd><a href="https://omia.org/results?search_type=advanced&omia_id=001777,001990" class="mim-tip-hint" title="OMIA" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OMIA', 'domain': 'omia.angis.org.au'})">OMIA</a></dd>
<dd><a href="https://wormbase.org/resources/disease/DOID:1612" 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': 'Wormbase Disease Ontology', 'domain': 'wormbase.org'})">Wormbase Disease Ontology</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Cell Lines</dt>
<dd><a href="https://catalog.coriell.org/Search?q=OmimNum:114480" class="definition" title="Coriell Cell Repositories; cell cultures and DNA derived from cell cultures." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'CCR', 'domain': 'ccr.coriell.org'})">Coriell</a></dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimLinksFold_2" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimDisorderCodesFold_2" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>SNOMEDCT: 254837009, 254843006</dd>
<dd>ICD10CM: C50, C50-C50</dd>
<dd>ORPHA: 227535</dd>
<dd>DO: 1612</dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimDisorderCodesFold_2" data-toggle="collapse">▲ Close</a>
</div>
</div>
</div>
</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
3:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/613347?search=113705%20114480%20600185%20604370%20612555%20613347%20614320&highlight=113705%2C114480%2C600185%2C604370%2C612555%2C613347%2C614320">
<span class="mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
613347.
</span>
PANCREATIC CANCER, SUSCEPTIBILITY TO, 2
</a>
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/13/83?start=-3&limit=10&highlight=83">
13q13.1</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">613347</span></span>
<br />
<a href="#mimPhenotypeMapFold_3" id="mimPhenotypeMapToggle_3" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimPhenotypeMapToggleTriangle_3" class="mimPingletonToggleTriangle" style="color: DarkOrchid">►</span> Phenotype-Gene Relationships</span></a>
<a href="#mimDisorderCodesFold_3" id="mimDisorderCodesToggle_3" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_3" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_3" id="mimLinksToggle_3" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_3" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimPhenotypeMapFold_3" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Phenotype-Gene Relationships
</caption>
<thead>
<tr>
<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/13/83?start=-3&limit=10&highlight=83">
13q13.1
</a>
</span>
</td>
<td>
<span class="mim-font">
{Pancreatic cancer 2}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613347"> 613347 </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">
BRCA2
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600185"> 600185 </a>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimPhenotypeMapFold_3" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimLinksFold_3" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=613347[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></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3708&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://clinicaltrials.gov/search?cond=PANCREATIC CANCER" class="mim-tip-hint" title="A registry of federally and privately supported clinical trials conducted in the United States and around the world." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3708&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/books/NBK1247/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></dd>
<dd><a href="https://www.diseaseinfosearch.org/x/9069" 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></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=613347[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></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=1333" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimLinksFold_3" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimDisorderCodesFold_3" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>ORPHA: 1333</dd>
</dl>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimDisorderCodesFold_3" data-toggle="collapse">▲ Close</a>
</div>
</div>
</div>
</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
4:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/612555?search=113705%20114480%20600185%20604370%20612555%20613347%20614320&highlight=113705%2C114480%2C600185%2C604370%2C612555%2C613347%2C614320">
<span class="mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
612555.
</span>
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2
</a>
</span>
<br />
<span class="mim-font">BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2, INCLUDED</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/13/83?start=-3&limit=10&highlight=83">
13q13.1</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">612555</span></span>
<br />
<a href="#mimPhenotypeMapFold_4" id="mimPhenotypeMapToggle_4" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimPhenotypeMapToggleTriangle_4" class="mimPingletonToggleTriangle" style="color: DarkOrchid">►</span> Phenotype-Gene Relationships</span></a>
<a href="#mimPhenotypicSeriesFold_4" id="mimPhenotypicSeriesToggle_4" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'PhenotypicSeries'})"><span class="small"><span id="mimPhenotypicSeriesToggleTriangle_4" class="mimSingletonToggleTriangle" style="color: #47B7D9">►</span> Phenotypic Series</span></a>
<a href="#mimDisorderCodesFold_4" id="mimDisorderCodesToggle_4" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_4" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_4" id="mimLinksToggle_4" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_4" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimPhenotypeMapFold_4" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Phenotype-Gene Relationships
</caption>
<thead>
<tr>
<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/13/83?start=-3&limit=10&highlight=83">
13q13.1
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast-ovarian cancer, familial, 2}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612555"> 612555 </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">
BRCA2
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600185"> 600185 </a>
</span>
</td>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimPhenotypeMapFold_4" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimPhenotypicSeriesFold_4" 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>
Breast-ovarian cancer, familial, susceptibility to
- <a href="/phenotypicSeries/PS604370">PS604370</a>
- 5 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/13/83?start=-3&limit=10&highlight=83"> 13q13.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612555"> {Breast-ovarian cancer, familial, 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/612555"> 612555 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600185"> BRCA2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600185"> 600185 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/278?start=-3&limit=10&highlight=278"> 16p12.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620442"> {Breast-ovarian cancer, familial, susceptibility to, 5} </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/620442"> 620442 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610355"> PALB2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610355"> 610355 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/415?start=-3&limit=10&highlight=415"> 17q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614291"> {Breast-ovarian cancer, familial, susceptibility to, 4} </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/614291"> 614291 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602954"> RAD51D </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602954"> 602954 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/610?start=-3&limit=10&highlight=610"> 17q21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604370"> {Breast-ovarian cancer, familial, 1} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Multifactorial">Mu</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/604370"> 604370 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/113705"> BRCA1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/113705"> 113705 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/792?start=-3&limit=10&highlight=792"> 17q22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613399"> {Breast-ovarian cancer, familial, susceptibility to, 3} </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/613399"> 613399 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602774"> RAD51C </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602774"> 602774 </a>
</span>
</td>
</tr>
</tbody>
</table>
</div>
<div class="text-right small">
<a href="#mimPhenotypicSeriesFold_4" data-toggle="collapse">▲ Close</a>
</div>
</div>
</div>
<div id="mimLinksFold_4" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=612555[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></dd>
<dd>EuroGentest</dd>
<dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3384&Typ=Pat" title="Hereditary breast and/or ovarian cancer syndrome" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast and/or o… </a></dd><dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=19054&Typ=Pat" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast cancer </a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://clinicaltrials.gov/search?cond=BREAST-OVARIAN CANCER, FAMILIAL" class="mim-tip-hint" title="A registry of federally and privately supported clinical trials conducted in the United States and around the world." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></dd>
<dd>EuroGentest</dd>
<dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3384&Typ=Pat" title="Hereditary breast and/or ovarian cancer syndrome" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast and/or o… </a></dd><dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=19054&Typ=Pat" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast cancer </a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/books/NBK1247/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></dd>
<dd><a href="https://www.diseaseinfosearch.org/x/7866" 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></dd>
<dd><a href="https://medlineplus.gov/genetics/condition/breast-cancer" class="mim-tip-hint" title="Consumer-friendly information about the effects of genetic variation on human health." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MedlinePlus Genetics', 'domain': 'medlineplus.gov'})">MedlinePlus Genetics</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=612555[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></dd>
<dd>OrphaNet</dd>
<dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=145" title="Hereditary breast and/or ovarian cancer syndrome" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">Hereditary breast and/or o…</a></dd><dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=227535" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">Hereditary breast cancer</a></dd>
</dl>
</td>
</tr>
</tbody>
</table>
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<a href="#mimLinksFold_4" data-toggle="collapse">▲ Close</a>
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</div>
<div id="mimDisorderCodesFold_4" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>ORPHA: 145, 227535</dd>
</dl>
</td>
</tr>
</tbody>
</table>
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<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
5:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/600185?search=113705%20114480%20600185%20604370%20612555%20613347%20614320&highlight=113705%2C114480%2C600185%2C604370%2C612555%2C613347%2C614320">
<span class="mim-tip-hint" title="Gene description">
<span class="text-danger"><strong>*</strong></span>
600185.
</span>
BRCA2 DNA REPAIR-ASSOCIATED PROTEIN; BRCA2
</a>
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/13/83?start=-3&limit=10&highlight=83">
13q13.1</a></span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font"><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&position=chr13:32315077-32400268&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'})">13:32,315,077-32,400,268</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">600185</span></span>
<br />
<a href="#mimGeneMapFold_5" id="mimGeneMapToggle_5" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimGeneMapToggleTriangle_5" class="mimSingletonToggleTriangle" style="color: DarkOrchid">►</span> Gene-Phenotype Relationships</span></a>
<a href="#mimDisorderCodesFold_5" id="mimDisorderCodesToggle_5" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_5" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_5" id="mimLinksToggle_5" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_5" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimGeneMapFold_5" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Gene-Phenotype Relationships
</caption>
<thead>
<tr>
<th>
Location
</th>
<th>
Phenotype
</th>
<th>
Phenotype <br /> MIM number
</th>
<th>
Inheritance
</th>
<th>
Phenotype <br /> mapping key
</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="8">
<span class="mim-font">
<a href="/geneMap/13/83?start=-3&limit=10&highlight=83">
13q13.1
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast cancer, male, susceptibility to}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/114480"> 114480 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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>
</tr>
<tr>
<td>
<span class="mim-font">
{Breast-ovarian cancer, familial, 2}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612555"> 612555 </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>
</tr>
<tr>
<td>
<span class="mim-font">
{Glioblastoma 3}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613029"> 613029 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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>
</tr>
<tr>
<td>
<span class="mim-font">
{Medulloblastoma}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/155255"> 155255 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Autosomal recessive">AR</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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>
</tr>
<tr>
<td>
<span class="mim-font">
{Pancreatic cancer 2}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613347"> 613347 </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>
</tr>
<tr>
<td>
<span class="mim-font">
{Prostate cancer}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/176807"> 176807 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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>
</tr>
<tr>
<td>
<span class="mim-font">
Fanconi anemia, complementation group D1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/605724"> 605724 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal recessive">AR</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>
</tr>
<tr>
<td>
<span class="mim-font">
Wilms tumor
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/194070"> 194070 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Somatic mutation">SMu</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>
</tr>
</tbody>
</table>
<div class="text-right small">
<a href="#mimGeneMapFold_5" data-toggle="collapse">▲ Close</a>
</div>
</div>
<div id="mimLinksFold_5" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=600185[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></dd>
</dl>
</td>
<td>
<dl>
<dt>Genome</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Location/View?db=core;g=ENSG00000139618;t=ENST00000380152" class="mim-tip-hint" title="Genome databases for vertebrates and other eukaryotic species." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/genome/gdv/browser/gene/?id=675" class="mim-tip-hint" title="Detailed views of the complete genomes of selected organisms from vertebrates to protozoa." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Genome Viewer', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Genome Viewer</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=600185" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>DNA</dt>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Transcript/Sequence_cDNA?db=core;g=ENSG00000139618;t=ENST00000380152" class="mim-tip-hint" title="Transcript-based views for coding and noncoding DNA." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Ensembl', 'domain': 'ensembl.org'})">Ensembl (MANE Select)</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_000059,NM_001406719,NM_001406720,NM_001406721,NM_001406722,NM_001432077,NR_176251" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/nuccore/NM_000059" class="mim-tip-hint" title="A collection of genome, gene, and transcript sequence data from several sources, including GenBank, RefSeq." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI RefSeq (MANE)', 'domain': 'ncbi.nlm.nih'})">NCBI RefSeq (MANE Select)</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgTracks?db=hg38&hgFind=omimGeneAcc&position=600185" 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'})">UCSC Genome Browser</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Protein</dt>
<dd><a href="https://hprd.org/summary?hprd_id=02554&isoform_id=02554_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></dd>
<dd><a href="https://www.proteinatlas.org/search/BRCA2" 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></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/protein/1161384,1177438,2315186,11276061,11276063,12034851,13540359,16116616,23506223,24431156,24431158,24431160,24431162,24431164,24431166,24431168,24431170,24431172,24431174,24431176,24431178,24431180,24431182,24431191,24431193,24431195,24431197,24431199,24431201,24431203,24431205,24431207,24431209,24431211,24431213,37675289,71064155,114432132,116256779,119628904,119628905,119628906,187233949,408773052,408773054,408773056,408773058,408773060,408773062,408773064,408773066,408773068,408773070,408773072,655203996,655204001,655204009,655204013,655204017,655204021,655204026,655204031,655204035,655204040,655204061,655204374,655204416,655204443,655204489,655204521,655204539,655204570,655204597,655204616,655204657,655204672,655205039,655205091,655205092,655205093,655205150,655205169,727705129,815932495,815932497,815932499,815932501,815932503,815932505,815932507,815932509,815932511,815932513,815932515,815932517,815932519,815932521,819327359,819327361,958168067,958168069,958168071,958168073,958168075,958168077,958168081,958168083,958168085,1147163652,1237408064,1238813711,1238813713,1238813715,1238813717,1238813719,1238813721,1238813723,1238813725,1238813727,1238813729,1238813731,1238813733,1388694386,1388694388,1388694390,1483525183,1483525185,1483525187,1483525189,1483525191,1483525193,1483525195,1483525197,1483525199,1483525201,1483525203,1483525205,1483525207,1483525209,1483525211,1483525213,1483525215,1483525217,1483525219,1483525221,1483525223,1483525225,1483525227,1483525229,1483525231,1483525233,1483525235,1483525237,1483525239,1483525241,1483525243,1483525245,1483525247,1483525249,1483525251,1483525266,1483525268,1483525270,1483525271,1483525273,1633439653,1633439655,1633439657,1633439659,1775781152,1775781154,1775781156,1775781158,1813836565,1821655617,1821655619,1889924844,1896049798,1896049800,1899341482,1899341484,2001548938,2001548973,2028478947,2029084601,2029084603,2029084605,2029084607,2029084609,2029084611,2029084613,2043420624,2043420691,2043420693,2043420695,2043420697,2043420699,2043420701,2043420703,2043420705,2043420707,2043420709,2043420711,2043420713,2043420715,2043420717,2043420719,2043420721,2043420723,2043420725,2043420727,2043420729,2043420731,2043420733,2043420735,2043420737,2043420739,2043420741,2043420743,2043420745,2043420747,2043420749,2043420751,2043420753,2043420755,2043420757,2043420759,2043420761,2043420828,2043420830,2043420897,2043420899,2094552266,2094552268,2094552274,2164862745,2164862753,2164862755,2164862805,2164862807,2164862809,2164862811,2164862813,2164862815,2164862817,2164862819,2165384314,2165384316,2178104973,2178104975,2178104977,2178105004,2178105244,2178105246,2178105248,2178105250,2178105577,2178105579,2178105581,2178105583,2178105585,2203400801,2218469244,2218469246,2218469248,2218469256,2218469260,2218469264,2218469270,2240897237,2240897241,2240897267,2240897269,2301582623,2301582625,2301582627,2301582629,2301582681,2301582683,2301582685,2301582687,2301582689,2301582691,2301582693,2301582695,2301582697,2301582699,2301582701,2396616330,2396616332,2396616405,2577097962,2607637286,2607637288,2703623460,2703623462,2703623464,2703623466,2703623468,2703623470,2703623472,2703623474,2703623476,2703623478,2703623480,2703623482,2703623484,2703623486,2703623488,2703623490,2778098788,2909903175" 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></dd>
<dd><a href="https://www.uniprot.org/uniprotkb/P51587" 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></dd>
</dl>
</td>
<td>
<dl>
<dt>Gene Info</dt>
<dd><a href="http://biogps.org/#goto=genereport&id=675" 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></dd>
<dd><a href="https://www.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=ENSG00000139618;t=ENST00000380152" 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></dd>
<dd><a href="https://www.genecards.org/cgi-bin/carddisp.pl?gene=BRCA2" 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></dd>
<dd><a href="http://amigo.geneontology.org/amigo/search/annotation?q=BRCA2" 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></dd>
<dd><a href="https://www.genome.jp/dbget-bin/www_bget?hsa+675" 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></dd>
<dd><a href="http://v1.marrvel.org/search/gene/BRCA2" 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:675" class="mim-tip-hint" title="Monarch Initiative." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Monarch', 'domain': 'monarchinitiative.org'})">Monarch</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/675" class="mim-tip-hint" title="Gene-specific map, sequence, expression, structure, function, citation, and homology data." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'NCBI Gene', 'domain': 'ncbi.nlm.nih.gov'})">NCBI Gene</a></dd>
<dd><a href="https://genome.ucsc.edu/cgi-bin/hgGene?db=hg38&hgg_chrom=chr13&hgg_gene=ENST00000380152.8&hgg_start=32315077&hgg_end=32400268&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></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://search.clinicalgenome.org/kb/gene-dosage/HGNC:1101" class="mim-tip-hint" title="A ClinGen curated resource of genes and regions of the genome that are dosage sensitive and should be targeted on a cytogenomic array." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ClinGen Dosage', 'domain': 'dosage.clinicalgenome.org'})">ClinGen Dosage</a></dd>
<dd><a href="https://search.clinicalgenome.org/kb/genes/HGNC:1101" 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></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=600185[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></dd>
</dl>
</td>
<td>
<dl>
<dt>Variation</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/clinvar?term=600185[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></dd>
<dd><a href="https://gnomad.broadinstitute.org/gene/ENSG00000139618" 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></dd>
<dd><a href="https://www.ebi.ac.uk/gwas/search?query=BRCA2" 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 </a></dd>
<dd><a href="https://www.gwascentral.org/search?q=BRCA2" 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 </a></dd>
<dd><a href="http://www.hgmd.cf.ac.uk/ac/gene.php?gene=BRCA2" class="mim-tip-hint" title="Human Gene Mutation Database; published mutations causing or associated with human inherited disease; disease-associated/functional polymorphisms." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'HGMD', 'domain': 'hgmd.cf.ac.uk'})">HGMD</a></dd>
<dd>Locus Specific DBs</dd>
<dd style="margin-left: 0.5em;"><a href="http://chromium.liacs.nl/LOVD2/cancer/home.php?select_db=BRCA2" title="LOVD - BReast CAncer 2 - literature unclassified variants (BRCA2)" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">LOVD - BReast CAncer 2 - l…</a></dd><dd style="margin-left: 0.5em;"><a href="http://databases.lovd.nl/genomed/home.php?select_db=BRCA2" title="Zhejiang University-Adinovo Center BRCA2 Database" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">Zhejiang University-Adinov…</a></dd><dd style="margin-left: 0.5em;"><a href="http://research.nhgri.nih.gov/bic/" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">Breast Cancer</a></dd><dd style="margin-left: 0.5em;"><a href="http://www.rockefeller.edu/fanconi/mutate/" title="Fanconi Anaemia Mutation Database" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Locus Specific DB', 'domain': 'locus-specific-db.org'})">Fanconi Anaemia Mutation D…</a></dd>
<dd><a href="https://evs.gs.washington.edu/EVS/PopStatsServlet?searchBy=Gene+Hugo&target=BRCA2&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></dd>
<dd><a href="https://www.pharmgkb.org/gene/PA25412" 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></dd>
</dl>
</td>
<td>
<dl>
<dt>Animal Models</dt>
<dd><a href="https://www.alliancegenome.org/gene/HGNC:1101" 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></dd>
<dd><a href="https://www.mousephenotype.org/data/genes/MGI:109337" class="mim-tip-hint" title="International Mouse Phenotyping Consortium." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'IMPC', 'domain': 'knockoutmouse.org'})">IMPC</a></dd>
<dd><a href="http://v1.marrvel.org/search/gene/BRCA2#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></dd>
<dd><a href="http://www.informatics.jax.org/marker/MGI:109337" 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></dd>
<dd><a href="https://www.mmrrc.org/catalog/StrainCatalogSearchForm.php?search_query=MGI:109337" class="mim-tip-hint" title="Mutant Mouse Resource & Research Centers." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'MMRRC', 'domain': 'mmrrc.org'})">MMRRC</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gene/675/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></dd>
<dd><a href="https://www.orthodb.org/?ncbi=675" class="mim-tip-hint" title="Hierarchical catalogue of orthologs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrthoDB', 'domain': 'orthodb.org'})">OrthoDB</a></dd>
<dd><a href="https://zfin.org/ZDB-GENE-060510-3" class="mim-tip-hint" title="The Zebrafish Model Organism Database." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'ZFin', 'domain': 'zfin.org'})">ZFin</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Cell Lines</dt>
<dd><a href="https://catalog.coriell.org/Search?q=OmimNum:600185" class="definition" title="Coriell Cell Repositories; cell cultures and DNA derived from cell cultures." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'CCR', 'domain': 'ccr.coriell.org'})">Coriell</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Cellular Pathways</dt>
<dd><a href="https://www.genome.jp/dbget-bin/get_linkdb?-t+pathway+hsa:675" 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></dd>
<dd><a href="https://reactome.org/content/query?q=BRCA2&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></dd>
</dl>
</td>
</tr>
</tbody>
</table>
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<a href="#mimLinksFold_5" data-toggle="collapse">▲ Close</a>
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</div>
<div id="mimDisorderCodesFold_5" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>SNOMEDCT: 1156923005, 25081006, 302849000, 399068003, 443333004</dd>
<dd>ICD10CM: C61</dd>
<dd>ICD9CM: 185</dd>
</dl>
</td>
</tr>
</tbody>
</table>
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<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
6:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/604370?search=113705%20114480%20600185%20604370%20612555%20613347%20614320&highlight=113705%2C114480%2C600185%2C604370%2C612555%2C613347%2C614320">
<span class="mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
604370.
</span>
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1
</a>
</span>
<br />
<span class="mim-font">BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1, INCLUDED</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/17/610?start=-3&limit=10&highlight=610">
17q21.31</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">604370</span></span>
<br />
<a href="#mimPhenotypeMapFold_6" id="mimPhenotypeMapToggle_6" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimPhenotypeMapToggleTriangle_6" class="mimPingletonToggleTriangle" style="color: DarkOrchid">►</span> Phenotype-Gene Relationships</span></a>
<a href="#mimPhenotypicSeriesFold_6" id="mimPhenotypicSeriesToggle_6" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'PhenotypicSeries'})"><span class="small"><span id="mimPhenotypicSeriesToggleTriangle_6" class="mimSingletonToggleTriangle" style="color: #47B7D9">►</span> Phenotypic Series</span></a>
<a href="#mimDisorderCodesFold_6" id="mimDisorderCodesToggle_6" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_6" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_6" id="mimLinksToggle_6" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_6" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimPhenotypeMapFold_6" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Phenotype-Gene Relationships
</caption>
<thead>
<tr>
<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/17/610?start=-3&limit=10&highlight=610">
17q21.31
</a>
</span>
</td>
<td>
<span class="mim-font">
{Breast-ovarian cancer, familial, 1}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604370"> 604370 </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Multifactorial">Mu</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">
BRCA1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/113705"> 113705 </a>
</span>
</td>
</tr>
</tbody>
</table>
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<div class="col-lg-12 col-md-12 col-sm-12 col-xs-12">
<h5>
Breast-ovarian cancer, familial, susceptibility to
- <a href="/phenotypicSeries/PS604370">PS604370</a>
- 5 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/13/83?start=-3&limit=10&highlight=83"> 13q13.1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/612555"> {Breast-ovarian cancer, familial, 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/612555"> 612555 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600185"> BRCA2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/600185"> 600185 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/16/278?start=-3&limit=10&highlight=278"> 16p12.2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/620442"> {Breast-ovarian cancer, familial, susceptibility to, 5} </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/620442"> 620442 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610355"> PALB2 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/610355"> 610355 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/415?start=-3&limit=10&highlight=415"> 17q12 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614291"> {Breast-ovarian cancer, familial, susceptibility to, 4} </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/614291"> 614291 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602954"> RAD51D </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602954"> 602954 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/610?start=-3&limit=10&highlight=610"> 17q21.31 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/604370"> {Breast-ovarian cancer, familial, 1} </a>
</span>
</td>
<td>
<span class="mim-font">
<abbr class="mim-tip-hint" title="Autosomal dominant">AD</abbr>, <abbr class="mim-tip-hint" title="Multifactorial">Mu</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/604370"> 604370 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/113705"> BRCA1 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/113705"> 113705 </a>
</span>
</td>
</tr>
<tr>
<td>
<span class="mim-font">
<a href="/geneMap/17/792?start=-3&limit=10&highlight=792"> 17q22 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/613399"> {Breast-ovarian cancer, familial, susceptibility to, 3} </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/613399"> 613399 </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602774"> RAD51C </a>
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/602774"> 602774 </a>
</span>
</td>
</tr>
</tbody>
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<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=604370[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></dd>
<dd>EuroGentest</dd>
<dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3384&Typ=Pat" title="Hereditary breast and/or ovarian cancer syndrome" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast and/or o… </a></dd><dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=19054&Typ=Pat" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast cancer </a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://clinicaltrials.gov/search?cond=BREAST-OVARIAN CANCER, FAMILIAL" class="mim-tip-hint" title="A registry of federally and privately supported clinical trials conducted in the United States and around the world." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></dd>
<dd>EuroGentest</dd>
<dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3384&Typ=Pat" title="Hereditary breast and/or ovarian cancer syndrome" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast and/or o… </a></dd><dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=19054&Typ=Pat" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">Hereditary breast cancer </a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/books/NBK1247/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></dd>
<dd><a href="https://www.diseaseinfosearch.org/x/7865" 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></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=604370[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></dd>
<dd>OrphaNet</dd>
<dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=145" title="Hereditary breast and/or ovarian cancer syndrome" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">Hereditary breast and/or o…</a></dd><dd style="margin-left: 0.5em;"><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=227535" target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">Hereditary breast cancer</a></dd>
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<div id="mimDisorderCodesFold_6" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>ORPHA: 145, 227535</dd>
</dl>
</td>
</tr>
</tbody>
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7:
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<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<a href="/entry/614320?search=113705%20114480%20600185%20604370%20612555%20613347%20614320&highlight=113705%2C114480%2C600185%2C604370%2C612555%2C613347%2C614320">
<span class="mim-tip-hint" title="Phenotype description, molecular basis known">
<span class="text-danger"><strong>#</strong></span>
614320.
</span>
PANCREATIC CANCER, SUSCEPTIBILITY TO, 4; PNCA4
</a>
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">
<a href="/geneMap/17/610?start=-3&limit=10&highlight=610">
17q21.31</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">614320</span></span>
<br />
<a href="#mimPhenotypeMapFold_7" id="mimPhenotypeMapToggle_7" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'GeneMap'})"><span class="small"><span id="mimPhenotypeMapToggleTriangle_7" class="mimPingletonToggleTriangle" style="color: DarkOrchid">►</span> Phenotype-Gene Relationships</span></a>
<a href="#mimDisorderCodesFold_7" id="mimDisorderCodesToggle_7" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'ICD+'})"><span class="small"><span id="mimDisorderCodesToggleTriangle_7" class="mimSingletonToggleTriangle" style="color: DarkRed">►</span> ICD+</span></a>
<a href="#mimLinksFold_7" id="mimLinksToggle_7" class="mimSingletonFoldToggle" data-toggle="collapse" onclick="gtag('event', 'mim_unfurl', {'fold': 'Links'})"><span class="small"><span id="mimLinksToggleTriangle_7" class="mimSingletonToggleTriangle" style="color: #337CB5">►</span> Links</span></a>
<div id="mimPhenotypeMapFold_7" class="well well-sm collapse mimSingletonToggleFold">
<table class="table table-bordered table-condensed small mim-table-padding">
<caption>
Phenotype-Gene Relationships
</caption>
<thead>
<tr>
<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/17/610?start=-3&limit=10&highlight=610">
17q21.31
</a>
</span>
</td>
<td>
<span class="mim-font">
{Pancreatic cancer, susceptibility to, 4}
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/614320"> 614320 </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">
BRCA1
</span>
</td>
<td>
<span class="mim-font">
<a href="/entry/113705"> 113705 </a>
</span>
</td>
</tr>
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<table class="table table-condensed small mim-table-padding ">
<caption>
Links
</caption>
<tbody>
<tr>
<td>
<dl>
<dt>Testing</dt>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=614320[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></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3708&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
</dl>
</td>
<td>
<dl>
<dt>Clinical Resources</dt>
<dd><a href="https://clinicaltrials.gov/search?cond=PANCREATIC CANCER" class="mim-tip-hint" title="A registry of federally and privately supported clinical trials conducted in the United States and around the world." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Clinical Trials', 'domain': 'clinicaltrials.gov'})">Clinical Trials</a></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/ClinicalLabs_Search_Simple.php?lng=EN&LnkId=3708&Typ=Pat" class="mim-tip-hint" title="A list of European laboratories that offer genetic testing." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'EuroGentest', 'domain': 'orpha.net'})">EuroGentest</a></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/books/NBK1247/" class="mim-tip-hint" title="Expert-authored, peer-reviewed descriptions of inherited disorders including the uses of genetic testing in diagnosis, management, and genetic counseling." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'Gene Reviews', 'domain': 'ncbi.nlm.nih.gov'})">Gene Reviews</a></dd>
<dd><a href="https://www.diseaseinfosearch.org/x/9071" 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></dd>
<dd><a href="https://www.ncbi.nlm.nih.gov/gtr/all/tests/?term=614320[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></dd>
<dd><a href="https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=1333" class="mim-tip-hint" title="European reference portal for information on rare diseases and orphan drugs." target="_blank" onclick="gtag('event', 'mim_outbound', {'name': 'OrphaNet', 'domain': 'orpha.net'})">OrphaNet</a></dd>
</dl>
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<table class="table table-condensed small mim-table-padding">
<caption>
ICD+
</caption>
<tbody>
<tr>
<td>
<dl>
<dd>ORPHA: 1333</dd>
</dl>
</td>
</tr>
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Search: <span class="mim-text-font">113705 114480 600185 604370 612555 613347 614320 (Search in: MIM number)</span>
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Results: 7 entries.
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<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
1:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<span class="text-danger"><strong>*</strong></span>
113705.
BRCA1 DNA REPAIR-ASSOCIATED PROTEIN; BRCA1
</span>
<br />
<span class="text-muted">
Cytogenetic location: <span class="mim-font">17q21.31</span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font">17:43,044,295-43,170,327</span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">113705</span></span>
</div>
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<div class="row">
<p />
</div>
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<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
2:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<span class="text-danger"><strong>#</strong></span>
114480.
BREAST CANCER
</span>
<br />
<span class="mim-font">BREAST CANCER, FAMILIAL MALE, INCLUDED</span>
<br />
<span class="text-muted">
Cytogenetic locations:
<span class="mim-font">1p34.1</a></span>,
<span class="mim-font">2q33.1</a></span>,
<span class="mim-font">2q35</a></span>,
<span class="mim-font">3q26.32</a></span>,
<span class="mim-font">5q34</a></span>,
<span class="mim-font">6p25.2</a></span>,
<span class="mim-font">6q25.1-q25.2</a></span>,
<span class="mim-font">8q11.23</a></span>,
<span class="mim-font">11p15.4</a></span>,
<span class="mim-font">11q22.3</a></span>,
<span class="mim-font">12p12.1</a></span>,
<span class="mim-font">13q13.1</a></span>,
<span class="mim-font">14q32.33</a></span>,
<span class="mim-font">14q32.33</a></span>,
<span class="mim-font">15q15.1</a></span>,
<span class="mim-font">16q22.1</a></span>,
<span class="mim-font">17p13.1</a></span>,
<span class="mim-font">17q21.33</a></span>,
<span class="mim-font">17q23.2</a></span>,
<span class="mim-font">17q23.2</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">114480</span></span>
</div>
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<p />
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3:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<span class="text-danger"><strong>#</strong></span>
613347.
PANCREATIC CANCER, SUSCEPTIBILITY TO, 2
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">13q13.1</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">613347</span></span>
</div>
</div>
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<p />
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4:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<span class="text-danger"><strong>#</strong></span>
612555.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2; BROVCA2
</span>
<br />
<span class="mim-font">BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2, INCLUDED</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">13q13.1</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">612555</span></span>
</div>
</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
5:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<span class="text-danger"><strong>*</strong></span>
600185.
BRCA2 DNA REPAIR-ASSOCIATED PROTEIN; BRCA2
</span>
<br />
<span class="text-muted">
Cytogenetic location: <span class="mim-font">13q13.1</span>,
Genomic coordinates <span class="small">(GRCh38)</span>: <span class="mim-font">13:32,315,077-32,400,268</span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">600185</span></span>
</div>
</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
6:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<span class="text-danger"><strong>#</strong></span>
604370.
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1; BROVCA1
</span>
<br />
<span class="mim-font">BREAST CANCER, FAMILIAL, SUSCEPTIBILITY TO, 1, INCLUDED</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">17q21.31</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">604370</span></span>
</div>
</div>
<div class="row">
<p />
</div>
<div class="row">
<div class="col-lg-1 col-md-1 col-sm-1 col-xs-1" style="width: 2em;">
7:
</div>
<div class="col-lg-11 col-md-11 col-sm-11 col-xs-11">
<span class="mim-result-font">
<span class="text-danger"><strong>#</strong></span>
614320.
PANCREATIC CANCER, SUSCEPTIBILITY TO, 4; PNCA4
</span>
<br />
<span class="text-muted">
Cytogenetic location:
<span class="mim-font">17q21.31</a></span>
</span>
<br />
<span class="text-success">Matching terms: <span class="mim-font">614320</span></span>
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