All individuals with variants in gene TPRN

27 entries on 1 page. Showing entries 1 - 27.
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AscendingIndividual ID     

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Population     

Age at death     

VIP     

Data_av     

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Disease     

Phenotype details     

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Owner     
00043836 - - DFNA9 M - Korea, South (Republic) Asian - - 52 - DFNA1 DFNA9 1 1 Han Sang Kim
00043837 - - DFNA9 M - Korea, South (Republic) Asian - - 48 - DFNA1 DFNA9 1 1 Han Sang Kim
00046602 PKDF1129/HLRB6 PubMed: Rehman 2010, Journal: Rehman 2010, PubMed: Naz 2017 5-generation family, 6 affecteds (F, 5M), unaffected heterozygous carriers parents/sibs - yes Pakistan Pakistani - - - - DFNB79 see paper; … 1 6 Jacopo Celli
00046603 - PubMed: Khan 2010 7-generation family, 17 affecteds (5F, 12M), unaffected heterozygous carriers parents/sibs - yes Pakistan Pakistani - - - - DFNB79 see paper; … 1 17 Jacopo Celli
00046604 - PubMed: Li 2010, Journal: Li 2010 5-generation family, 7 affecteds (6F, M), unaffected heterozygous carriers parents/sibs - yes Morocco Moroccan - - - - DFNB79 see paper; … 1 7 Jacopo Celli
00046605 - PubMed: Khan 2010 4-generation family, 4 affecteds (2F, 2M), unaffected heterozygous carriers parents/sibs M yes Pakistan Pakistani - - - - DFNB79 see paper; … 1 4 Jacopo Celli
00046606 - PubMed: Khan 2010 5-generation family, 5 affecteds (2F, 3M), unaffected heterozygous carriers parents/sibs - yes Pakistan Pakistani - - - - DFNB79 see paper; … 1 5 Jacopo Celli
00046607 - PubMed: Li 2010, Journal: Li 2010 2-generation family, 2 affecteds (F, M), unaffected heterozygous carriers parents - - Netherlands Dutch - - - - DFNB79 see paper; … 1 2 Jacopo Celli
00059154 - PubMed: Sommen 2016, Journal: Sommen 2016 - - - - - - - - - DFNB;ARNSHL - 1 1 Manou Sommen
00284146 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00284147 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00284148 - PubMed: Duzkale 2013 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00284149 - PubMed: Sloan-Heggen 2016 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284150 - PubMed: Li 2010 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284151 - PubMed: Rehman 2010 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284152 - PubMed: Rehman 2010 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284153 - PubMed: Sloan-Heggen 2016 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284154 - PubMed: Rehman 2010, PubMed: Li 2010 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284155 - PubMed: Rehman 2010, PubMed: Li 2010, PubMed: Bashir 2013 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00294818 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294819 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00327147 SB428-830 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - HL - 2 1 So Young Kim
00441163 HL007PatVII3 PubMed: Richard 2019 7-generation family, 11 affected (3F, 8M), seggregating two different genetic hearing loss condistions; 1 double affected individual M yes Pakistan - - - - - HL - 1 11 Johan den Dunnen
00441448 PKDF1756 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441449 PKDF1757 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441450 PKDF1758 PubMed: Richard 2019 - - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
00441460 HL007 PubMed: Richard 2019 individual (F) seggregating CDH23 associated hearing loss - yes Pakistan - - - - - HL - 1 1 Johan den Dunnen
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