All individuals with variants in gene ARL2BP

20 entries on 1 page. Showing entries 1 - 20.
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00155381 FamMOL0807 PubMed: Davidson 2013 4-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents/relatives M yes Israel Arab-Muslim - - - - retinal disease - 1 3 Dror Sharon
00233372 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 3 Yoshito Koyanagi
00233373 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233374 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00271385 FamGC19277 PubMed: Davidson 2013 5-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M yes Israel European - - - - HL, retinal disease primary ciliary dyskinesia, recurrent otitis media progressively affecting hearing, retinitis pigmentosa, respiratory failure from early age, required physiotherapy regularly through school years;20s-night-vision problems, ERG confirmed severe rod and /cone dysfunction, progressive loss peripheral vision and later central vision; visual acuities right 0.25/left 0.5, visual fields constricted to 10, fundus examination revealed widespread retinal degeneration with only sparse bone-spicule pigmentation 1 1 Johan den Dunnen
00271386 FamPatCIC01154 PubMed: Audo 2017 2-generation family, 2 affected sisters (2F), unaffected heterozygous carrier parents F yes Morocco - - - - - retinal disease 10s-moderately severe rod-cone dystrophy; 36y-best corrected visual acuity right 20/200 and left counting finger, visual fields <10 degrees; fundus examination typical rod-cone dystrophy signs, atrophic macular changes, X-rays chest no situs inversus 1 2 Johan den Dunnen
00271387 FamPatCIC01155 PubMed: Audo 2017 - F - Morocco - - - - - retinal disease 10s-moderately severe rod-cone dystrophy; 2y best corrected visual acuity both eyes 20/25, visual fields reduced 30degrees 1 1 Johan den Dunnen
00271388 Fam1PatII4 PubMed: Fiorentino 2018 3-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F no United Kingdom (Great Britain) white - - - - retinal disease retinitis pigmentosa, no syndromic features 1 1 Johan den Dunnen
00271389 Fam2PatIII2 PubMed: Fiorentino 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents/relatives M no United Kingdom (Great Britain) North African - - - - retinal disease see paper; ... 1 1 Johan den Dunnen
00308949 - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - retinal disease - 1 1 Global Variome, with Curator vacancy
00308950 - PubMed: Sharon 2019 5 IRD families - - Israel - - - - - retinal disease - 1 5 Global Variome, with Curator vacancy
00328097 G005193 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - retinal disease - 1 1 LOVD
00372650 RP245 PubMed: Xu 2014 family M - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372660 RP275 PubMed: Xu 2014 patient F - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372710 RP206 PubMed: Xu 2014 - - - China - - - - - retinal disease see paper; ... 1 1 LOVD
00383776 RD18073517_A PubMed: Gao 2019 - ? - China - - - - - retinal disease - 1 1 LOVD
00386226 RPN-404 PubMed: Rodriguez-Munoz 2020 - ? - Spain - - - - - retinal disease - 1 1 LOVD
00390166 G005193 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
00428030 A213 PubMed: Bournazos 2022 family, 1 affected - - Australia - - - - - ? - 1 1 Johan den Dunnen
00447298 SRP-1199 PubMed: Weisschuh 2024 patient, no family history M - Germany - - - - - ? - 1 1 Johan den Dunnen
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