All individuals with variants in gene PDE6G

20 entries on 1 page. Showing entries 1 - 20.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00155522 - Sharon, submitted - M yes Israel Arab-Muslim - - - - retinal disease - 1 1 Dror Sharon
00233498 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00233499 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00291895 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 51 Mohammed Faruq
00304613 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00309297 - PubMed: Sharon 2019 4 IRD families - - Israel - - - - - retinal disease - 1 4 Global Variome, with Curator vacancy
00309620 FamTB14 PubMed: Dvir 2010 extended 4-generation family, 6 affected (2F, 4M), unaffected heterozygous carrier parents/relatives F;M yes Israel Arab Muslim - - - - retinal disease see paper; ..., severe early-onset retinitis pigmentosa 1 1 Johan den Dunnen
00358963 Case71762 PubMed: Tiwari 2016 see paper F - Switzerland - - - - - retinal disease see paper; ... 1 1 LOVD
00359318 30120 PubMed: Khan 2017 see paper - - United Kingdom (Great Britain) - - - - - retinal disease see paper; ... 1 1 LOVD
00372651 RP382 PubMed: Xu 2014 patient F - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372652 RP331 PubMed: Xu 2014 patient M - China - - - - - retinal disease see paper; ... 1 1 LOVD
00372712 RP234 PubMed: Xu 2014 - - - China - - - - - retinal disease see paper; ... 1 1 LOVD
00376763 25 PubMed: Wang 2014 - M - United States - - - - - retinal disease - 1 1 LOVD
00384180 RP-3027 PubMed: Martin Merida 2019 - ? - Spain - - - - - retinal disease - 1 1 LOVD
00389531 815 PubMed: Weisschuh 2020 Filing key number: 332, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given F - Germany - - - - - retinal disease age at genetic diagnosis mentioned 1 1 LOVD
00407356 RP-95 PubMed: Borràs 2013 - - - Spain Spanish - - - - retinal disease - 1 1 LOVD
00429484 - PubMed: Panneman 2023 - F - - - - - - - RP - 1 1 Daan Panneman
00429980 - PubMed: Panneman 2023 - F - - - - - - - RP - 2 1 Daan Panneman
00430135 - PubMed: Panneman 2023 - M - - - - - - - RP - 1 1 Daan Panneman
00447664 CD-584 PubMed: Weisschuh 2024 family, 2 affected F - Germany - - - - - ? - 1 2 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.