All individuals with variants in gene GUCA1B

32 entries on 1 page. Showing entries 1 - 32.
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00033094 - - - M - - - - - - - retinal disease - 2 1 Kornelia Neveling
00033108 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033109 - PubMed: Neveling 2012 - F no - - - - - - retinal disease - 1 1 Kornelia Neveling
00033112 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033124 - - - F - - - - - - - retinal disease dystrophy, macular, juvenile 1 1 Kornelia Neveling
00033127 - - - F - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033145 - - - M - - - - - - - retinal disease - 1 1 Kornelia Neveling
00033154 - - - F - - - - - - - retinal disease epilepsy 1 1 Kornelia Neveling
00232683 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 23 Yoshito Koyanagi
00232684 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232685 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 3 Yoshito Koyanagi
00232686 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232687 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 6 Yoshito Koyanagi
00233687 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00299640 FamGC18203Pat1 PubMed: Arno 2017 3-generation family, 1 affeted, unaffected heterozygous carrier parents F - - - - - - - retinal disease see paper; ..., 20y-reduced acuity (HP:0007663), mild nyctalopia (HP:0000662), blind spots (HP:0000575); irregular peripheral pigment (HP:0007703), pale discs (HP:0000543), cystoid macular edema (HP:0011505), vitreous opacities (HP:0007648), attenuated sheathed vessels (HP:0007843), peripheral retinal exudate (HP:0001147); 30y-subnormal PERG, rod specific ERG markedly subnormal, bright flash subnormal with unusual bifid b waves, cone specific delayed and subnormal, profound rod>cone dysfunction; 29y-colour vision Ishihara R 17/17 L 13/17; 36y-octopus visual fields central 20-30 degrees retained on R, 30-50 degrees on L;37y 24-2 central scotomas, fields constricted to 15 degrees each eye; presenting VA logMAR (Snellen) R 0.3 (20/40), L 0.18 (20/30); latest VA logMAR R 0.6 (20/80), L 0.6 (20/80); latest refractive error, dioptres R 0/-0.50x100, L +1.00/-0.75x110 1 1 Johan den Dunnen
00328416 680602 PubMed: Zhou 2018 - - - China - - - - - retinal disease - 1 1 LOVD
00362006 Pat9AB PubMed: Duvvari 2016 patient - - Netherlands white - - - - retinal disease - 1 1 LOVD
00372645 RP289 PubMed: Xu 2014 patient F - China - - - - - retinal disease see paper; ... 1 1 LOVD
00373473 RP1728 PubMed: Fernandez-San Jose 2015 family, 2 affected - - Spain - - - - - retinal disease see paper; ... 1 2 LOVD
00373480 RP0992 PubMed: Fernandez-San Jose 2015 family, 2 affected - - Spain - - - - - retinal disease see paper; ... 1 2 LOVD
00376755 15 PubMed: Wang 2014 - M - United States - - - - - retinal disease - 1 1 LOVD
00377374 ? PubMed: Martin-Merida 2018 - - - Spain - - - - - retinal disease - 1 1 LOVD
00379426 - PubMed: Zhou 2011 - - - China - - - - - retinal disease - 1 1 LOVD
00382799 - PubMed: Song-2011 - F - - - - - - - retinal disease - 1 1 LOVD
00383796 RD18184091_B PubMed: Gao 2019 - ? - China - - - - - retinal disease - 1 1 LOVD
00386190 RPN-304 PubMed: Rodriguez-Munoz 2020 family fRPN-144, proband F - Spain - - - - - retinal disease - 1 1 LOVD
00386975 1 PubMed: Jauregui 2020 - M - (United States) white - - - - retinal disease - 1 1 LOVD
00395885 F229 PubMed: Chen 2021 - ? - Taiwan - - - - - retinal disease - 1 1 LOVD
00420535 F229 PubMed: Chen 2021 - - - Taiwan - - - - - retinal disease - 1 1 LOVD
00446964 ARRP-110 PubMed: Weisschuh 2024 family, 2 affected M - Germany - - - - - ? - 1 2 Johan den Dunnen
00447382 STGD-436 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - ? - 1 1 Johan den Dunnen
00447637 UD-118 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
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