All individuals with variants in gene OTOGL

26 entries on 1 page. Showing entries 1 - 26.
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00080144 - PubMed: Zazo Seco 2017, Journal: Zazo Seco 2017 - - - - - - - - - deafness - 2 1 Mieke Wesdorp
00228149 FamPatII3 PubMed: Mahfood 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents M yes United Arab Emirates - - - - - DFNB congenital bilateral profound sensorineural hearing loss 2 1 Johan den Dunnen
00284927 - PubMed: Yariz 2012 - - - - - - - - - HL - 1 1 Global Variome, with Curator vacancy
00284928 - PubMed: Yariz 2012 - - - - - - - - - HL - 1 1 Global Variome, with Curator vacancy
00284929 - PubMed: Bonnet 2013 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284930 - PubMed: Sloan-Heggen 2016 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284931 - PubMed: Lim 2013 - - - - - - - - - autism - 1 1 Global Variome, with Curator vacancy
00284932 - - - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284933 - PubMed: Bonnet 2013 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284934 - PubMed: Sloan-Heggen 2016 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284935 - - - - - - - - - - - HL - 1 1 Global Variome, with Curator vacancy
00284936 - PubMed: Yariz 2012 - - - - - - - - - HL - 1 1 Global Variome, with Curator vacancy
00284937 - PubMed: Lim 2013 - - - - - - - - - autism - 1 1 Global Variome, with Curator vacancy
00284938 - PubMed: Sloan-Heggen 2016 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00284939 - PubMed: Sloan-Heggen 2016 - - - - - - - - - deafness - 1 1 Global Variome, with Curator vacancy
00290798 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 34 Mohammed Faruq
00290799 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00290800 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00290801 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 79 Mohammed Faruq
00304380 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00304381 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00325869 - - - F - - - - - - - ? Hearing impairment (HP:0000365); Scotoma (HP:0000575); Keratoconjunctivitis sicca (HP:0001097); Migraine (HP:0002076) 1 1 IMGAG
00332253 FamF PubMed: Astuti 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents - yes Algeria - - - - - retinal disease see paper; ... 2 1 LOVD
00332411 - - - - - - - - - - - DFNB84B - 2 1 Gemeinschaftspraxis für Humangenetik Dresden
00398068 185896 - - F yes Germany - - - - - DFNB84B Hearing impairment 1 1 Andreas Laner
00459539 patient;PatB PubMed: Szczałuba 2018, PubMed: Chmielewska 2024 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Poland - - - - - NDD see paper; ..., pregnancy complicated by maternal kidney stones, hyperemesis; birth-37w cesarean section, weight 3580g (75th), length 56cm (50th), OFC 34cm (25th-50th); no congenital anomalies, no dysmorphic features; feeding difficulties, constipation, frequent infections, slightly raised body temperature, allergy to cow's milk; intellectual disability; developmental delay, autistic features; hypotonia; increased immunoglobulin E; 13m-delayed teeth eruption; neurologic sensory; MRI normal non-contrast; no muskuloskeletal anomalies; no cardiac anomalies 1 1 Johan den Dunnen
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