All individuals with variants in gene GJB2

324 entries on 4 pages. Showing entries 1 - 100.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 1 1 Yu Sun
00024124 - - 4 families, 10 affecteds - - Pakistan - - - - - DFNB;ARNSHL - 1 10 Atteeq Rehman
00024125 - - 2 families, 7 affecteds - - Pakistan - - - - - DFNB;ARNSHL - 1 7 Atteeq Rehman
00024126 - - 2 families, 10 affecteds - - (Pakistan) - - - - - DFNB;ARNSHL - 1 10 Atteeq Rehman
00024131 - PubMed: Estivill 1998, Journal: Estivill 1998 - ? ? Spain - - - - - DFNB1A - 1 1 Johan den Dunnen
00043755 - PubMed: del Castillo 2002, Journal: del Castillo 2002 2-generation family, affected mother and father (parents of daugthers II1/2) - no Spain - - - - - DFNB1A digenic inheritance; severe deafness 1 2 Johan den Dunnen
00043757 - PubMed: del Castillo 2005, Journal: del Castillo 2005 ARNSHI cases from Spain ? no Spain - - - - - DFNB1B di-geneic inheritance; autosomal recessive non-syndromic hearing impairment 1 10 Johan den Dunnen
00043762 - PubMed: Lerer 2001, Journal: Lerer 2001 2-generation family, affected daugther (II4), unaffected heterozygous carrier mother (father I1, brother II3) F no Israel Jewish-Ashkenazi - - - - DFNB;ARNSHL di-genic inheritance; non-syndromic hearing loss 1 3 Johan den Dunnen
00043763 - PubMed: Lerer 2001, Journal: Lerer 2001 2-generation family, affected son (II4), unaffected heterozygous carrier mother (father I1, sister II4) M no Israel Jewish-Ashkenazi - - - - DFNB;ARNSHL di-genic inheritance; non-syndromic hearing loss 1 1 Johan den Dunnen
00043764 - PubMed: Lerer 2001, Journal: Lerer 2001 2-generation family, affected father (I1), affected son (II3) and daugther (II4) M no Israel Jewish-Ashkenazi - - - - DFNB;ARNSHL - 2 1 Johan den Dunnen
00046611 - PubMed: Falk 2012; Journal: Falk 2012 4-generation family seggregating LCA and hearing loss, 7 affecteds (2 LCA, 2 hearing loss, 3 both), unaffected heterozygous carrier parents/sibs - yes Pakistan - - - - - DFNB1A, LCA see paper; ... 1 7 Johan den Dunnen
00050598 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? congenital sensorineural hearing impairment, autism, specific learning disability, abnormal facial shape, sparse eyebrow, full cheeks, thick lower lip vermilion, broad forehead 1 1 Johan den Dunnen
00059144 - PubMed: Sommen 2016, Journal: Sommen 2016 - - - - - - - - - DFNB;ARNSHL - 1 1 Manou Sommen
00060258 - PubMed: Behar 2014, Journal: Behar 2014 3-generation family, 2 affecteds (F, M), unaffected carrier parents/sibs; family segregates GJB2 and USH2A variants F;M no Israel Iraq;Jewish;Jewish-Ashkenazi - - - - USH2A Congenital, moderate HL; retinitis pigmentosa? 1 3 Zippi Brownstein
00060259 - PubMed: Behar 2014, Journal: Behar 2014 3-generation family, 1 affected, unaffected carrier parents/sibs; family segregates GJB2 and USH2A variants M no Israel Iraq;Jewish - - - - DFNB1A Congenital, profound NSHL 1 1 Zippi Brownstein
00080025 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080026 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080028 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080039 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080045 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080046 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080049 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080051 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00080057 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00081072 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - KIDAD Keratitis-ichthyosis-deafness syndrome (OMIM:148210) 1 1 Daniel Trujillano
00092242 - PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016 2-generation family, 1 affected, unaffected heterozygous carrier mother/unaffected homozygous carrier father M no United States Filipino - - - - ?, DFNB1A cardiomyopathy, sialicaciduria (may be benign), moderate stable sensorineural hearing loss 1 1 Johan den Dunnen
00104025 Vogelaar-716A PubMed: Vogelaar 2017, Journal: Vogelaar 2017 54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type gastric cancer - - - - - - - - cancer, gastric diffuse-type or intestinal-type gastric cancer 1 1 Marjolijn JL Ligtenberg
00117226 S1504 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117227 S1528 PubMed: Baux 2017, Journal: Baux 2017 Proband M - France - - - - - deafness - 1 1 David Baux
00117228 S1534 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117229 S1546 PubMed: Baux 2017, Journal: Baux 2017 Proband F - Algeria - - - - - deafness - 1 1 David Baux
00117230 S1547 PubMed: Baux 2017, Journal: Baux 2017 Proband M - - - - - - - deafness - 1 1 David Baux
00117231 S1550 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117232 S1563 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 2 1 David Baux
00117233 S1567 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00117234 S1577 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00117235 S1578 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? Turkey - - - - - deafness - 1 1 David Baux
00117236 S1579 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? - - - - - - deafness - 2 1 David Baux
00117237 S1584 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 1 1 David Baux
00117238 S1582 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? - - - - - - deafness - 2 1 David Baux
00117239 S1594 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00117240 S1599 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00117241 S1604 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117242 S1606 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117243 S1621 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117244 S1635 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00117245 S1636 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 1 1 David Baux
00117246 S1647 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00117247 S1654 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117248 S1674 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117249 S1685 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117250 S1686 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? - - - - - - deafness - 1 1 David Baux
00117251 S1589 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? Portugal - - - - - deafness - 1 1 David Baux
00117252 S1694 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 2 1 David Baux
00117253 S1705 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 2 1 David Baux
00117254 S1715 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117255 S1716 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 2 1 David Baux
00117256 S1720 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 1 1 David Baux
00117257 S1727 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117258 S1735 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117259 S1740 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117260 S1754 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 2 1 David Baux
00117261 S1760 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? - - - - - - deafness - 1 1 David Baux
00117262 S1768 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117263 S1771 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 2 1 David Baux
00117264 S1778 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 1 1 David Baux
00117265 S1790 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? Morocco - - - - - deafness - 1 1 David Baux
00117266 S1791 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 2 1 David Baux
00117267 S1795 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 2 1 David Baux
00117268 S1801 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117269 S1820 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117270 S1825 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117271 S1851 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00117272 S1854 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117273 S1857 PubMed: Baux 2017, Journal: Baux 2017 Proband F ? France - - - - - deafness - 1 1 David Baux
00117274 S1872 PubMed: Baux 2017, Journal: Baux 2017 Proband M no France - - - - - deafness - 2 1 David Baux
00117278 S1566 PubMed: Baux 2017, Journal: Baux 2017 Proband F no France - - - - - deafness - 1 1 David Baux
00117287 S1733 PubMed: Baux 2017, Journal: Baux 2017 Proband M ? France - - - - - deafness - 1 1 David Baux
00132291 FamPatIV2 PubMed: Eisenberger 2018 4-generation family, 8 affected (4F, 4M) M no Germany white - - - - DFNA see paper; ... 1 8 Hanno Bolz
00170804 S1679 PubMed: Baux 2017 Proband - Age 14 at the time of the study - possible USH2 F - France - - - - - DFN - 1 1 Anne-Françoise Roux
00181170 68944 - - M no Switzerland - - - - - EE - 2 1 Anaïs Begemann
00181181 24158611-Pat PubMed: Dalamon 2013 - M - Argentina - 22y - - - deafness hypoparathyroidism, congenital bilateral profound HI, cochlear implanted with good outcome 2 1 Viviana Karina Dalamón
00181208 24158611-Pat PubMed: Dalamon 2013 - M ? (Argentina) - ? - - cochlear implant deafness profound deafness 3 1 Viviana Karina Dalamón
00181210 24158611-Pat PubMed: Dalamon 2013 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M no Argentina - >30y - - - DFNB - 1 1 Viviana Karina Dalamón
00181222 24158611-Pat PubMed: Dalamon 2013 - M no Argentina - >02y - - - DFNB - 3 1 Viviana Karina Dalamón
00181514 - PubMed: del Castillo 2005, Journal: del Castillo 2005 ARNSHI cases - - Spain - - - - - DFNB1B di-geneic inheritance; autosomal recessive non-syndromic hearing impairment 1 1 Johan den Dunnen
00181516 - PubMed: del Castillo 2005, Journal: del Castillo 2005 ARNSHI cases - - Italy - - - - - DFNB1B di-geneic inheritance; autosomal recessive non-syndromic hearing impairment 1 1 Johan den Dunnen
00181517 - PubMed: del Castillo 2005, Journal: del Castillo 2005 ARNSHI cases - - United Kingdom (Great Britain) - - - - - DFNB1B di-geneic inheritance; autosomal recessive non-syndromic hearing impairment 1 4 Johan den Dunnen
00181518 - PubMed: del Castillo 2005, Journal: del Castillo 2005 ARNSHI cases - - Brazil - - - - - DFNB1B di-geneic inheritance; autosomal recessive non-syndromic hearing impairment 1 1 Johan den Dunnen
00182956 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (moderate) 1 1 Viviana Karina Dalamón
00182957 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (moderate) 1 1 Viviana Karina Dalamón
00182958 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (moderate) 1 1 Viviana Karina Dalamón
00182959 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (severe) 1 1 Viviana Karina Dalamón
00182960 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (severe) 1 1 Viviana Karina Dalamón
00182961 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (severe) 1 1 Viviana Karina Dalamón
00182962 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (profound) 1 1 Viviana Karina Dalamón
00182963 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (profound) 1 1 Viviana Karina Dalamón
00182964 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (profound) 1 1 Viviana Karina Dalamón
00182965 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (profound) 1 1 Viviana Karina Dalamón
00182966 24158611-Pat PubMed: Dalamon 2013 analysis 476 unrelated non-syndromic deaf individuals - - Argentina - - - - - deafness deafness (profound) 1 1 Viviana Karina Dalamón
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