All individuals with variants in gene GPR179

36 entries on 1 page. Showing entries 1 - 36.
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00087820 - PubMed: Audo 2012 - - - - - - - - - CSNB - 1 1 SIB - Livia Famiglietti
00087821 - PubMed: Audo 2012 - - - - - - - - - CSNB - 1 1 SIB - Livia Famiglietti
00087822 - PubMed: Audo 2012 - - - - - - - - - CSNB - 1 1 SIB - Livia Famiglietti
00087823 - PubMed: Audo 2012 - - - - - - - - - CSNB - 1 1 SIB - Livia Famiglietti
00088061 - - - F yes India Indian - - - - CSNB1E - 1 1 Soumittra Nagasamy
00291688 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00291690 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 10 Mohammed Faruq
00291691 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00291692 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00309836 - PubMed: Shah 2018 - F - United States white - - - - retinal disease see paper; ... 1 1 Johan den Dunnen
00327981 G001012 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00328859 Fam20289PatII1 PubMed: Zhong 2019 2-generation family, 1 affected, unaffected parents M no China - - - - - retinal disease see paper; ..., poor vision, nystagmus, pronounced maculopathy, peripheral hyperpigmentation, retinal vascular attenuation 1 1 LOVD
00332556 - - - M - - - - - - - ? Congenital stationary night blindness (HP:0007642) 1 1 IMGAG
00333359 Pat10 PubMed: Costa 2017 - F - Brazil - - - - - retinal disease see paper; ... 1 1 LOVD
00363662 11DG1962 PubMed: Patel 2016 - - - Saudi Arabia - - - - - retinal disease non-syndromic 1 1 LOVD
00363747 14DG0286 PubMed: Patel 2016 - - - Saudi Arabia - - - - - retinal disease non-syndromic 1 1 LOVD
00372498 171 PubMed: Wang 2015 index case - - China - - - - - retinal disease see paper; ... 1 1 LOVD
00375403 - PubMed: Zeitz 2015 - - - United Kingdom (Great Britain) - - - - - retinal disease see paper; ... 1 1 LOVD
00375404 - PubMed: Zeitz 2015 - - - United Kingdom (Great Britain) - - - - - retinal disease see paper; ... 1 1 LOVD
00375411 RP#002 PubMed: Katagiri 2014 family - - Japan - - - - - retinal disease see paper; ... 1 1 LOVD
00375432 RP#027 PubMed: Katagiri 2014 family - - Japan - - - - - retinal disease see paper; ... 1 1 LOVD
00376848 Pat3 PubMed: Malaichamy 2014 see paper - - India - - - - - retinal disease see paper; ... 1 1 LOVD
00381266 - PubMed: Bijveld-2013 1 female, 1 male - - Netherlands Dutch - - - - retinal disease - 1 2 Julia Lopez
00382549 411 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 2 1 LOVD
00382601 464 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - retinal disease - 1 1 LOVD
00384167 RP-2904 PubMed: Martin Merida 2019 - ? - Spain - - - - - retinal disease - 1 1 LOVD
00389080 364 PubMed: Weisschuh 2020 Filing key number: 122, congenital stationary night blindness, no patient Ids, consecutive numbers given M - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00390268 G001012 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - retinal disease - 1 1 LOVD
00391757 2.II:1 PubMed: DiScipio 2020 - M - - - - - - - retinal disease Right exotropia - infancy, Nyctalopia at 11 years, visual acuity right/left eye: 20/70: 20/40, Contrast Sensitivity: 1.65:165, Color vision: normal, Refractive error :-7.75+1.50 × 108:, -7.75+1.50 × 70, Tilted disc;, tessellated, background; dull, FR, Fundus autofluorescence: not done, Optical Coherence Tomography: normal central retinal thickness and laminati 1 1 LOVD
00413673 proband 1 PubMed: Peachey 2012 proband M - - - - - - - retinal disease best corrected visual acuity: 20/70 both eyes, mild myopic refractive error, congenital nystagmus, a history of early onset night blindness, a normal retinal appearance and full Goldmann visual fields; electroretinogram: dark-adapted conditions: the ERG b-wave recorded to a low luminance markedly reduced in amplitude, high flash luminance: robust a-wave without the subsequent b-wave seen in controls; light-adapted conditions: a square a-wave, retaining a late positive ERG component 2 1 LOVD
00413674 proband 2 PubMed: Peachey 2012 proband F - - Norwegian - - - - retinal disease rotatory nystagmus, a very unusual blond fundus, and congenital night blindness; best corrected visual acuity and refraction: 20/30 and - 12.00 D; electroretinogram: dark-adapted conditions: the ERG b-wave recorded to a low luminance markedly reduced in amplitude, high flash luminance: robust a-wave without the subsequent b-wave seen in controls; light-adapted conditions: a square a-wave, retaining a late positive ERG component 2 1 LOVD
00426936 40_48 PubMed: Zhu 2022 family 40, individual 48 M - - - - - - - retinal disease - 1 1 LOVD
00429589 - PubMed: Panneman 2023 - F - - - - - - - RP - 2 1 Daan Panneman
00447132 CSNB-146 PubMed: Weisschuh 2024 patient M - Germany - - - - - ? - 2 1 Johan den Dunnen
00447327 SRP-1283 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
00447717 SRP-1255 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - ? - 1 1 Johan den Dunnen
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