All individuals with variants in gene RP9

18 entries on 1 page. Showing entries 1 - 18.
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     
00033130 - - - M - - - - - - - retinal disease Wilm's tumor 1 1 Kornelia Neveling
00232843 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00232844 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1203 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00232845 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1198 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 2 Yoshito Koyanagi
00232846 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232847 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232848 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 1 Yoshito Koyanagi
00232849 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - retinal disease - 1 3 Yoshito Koyanagi
00325460 3335 PubMed: Zenteno 2020 - - - Mexico - - - - - retinal disease - 1 1 Johan den Dunnen
00331287 Pat41 PubMed: Maeda 2018 patient, no family history F - Japan - - - - - retinal disease - 1 1 LOVD
00335717 - PubMed: Sullivan 2006 - - - United States - - - - - retinal disease - 1 1 Julia Lopez
00372650 RP245 PubMed: Xu 2014 family M - China - - - - - retinal disease see paper; ... 1 1 LOVD
00375445 PatA PubMed: Watson 2014 family - - United Kingdom (Great Britain) - - - - - retinal disease see paper; ... 1 1 LOVD
00387389 9 PubMed: Sun 2020 - F - China - - - - - retinal disease no lens opacity, peripheral choroidal atrophy, negative family history, BCVA OD/OS: 0.6/0.5, hypotension 1 1 LOVD
00388508 15009450 PubMed: Ellingsford 2018 - - - United Kingdom (Great Britain) - - - - - retinal disease - 1 1 LOVD
00393621 - PubMed: Liu-2020 - M - - - - - - - retinal disease - 1 1 LOVD
00394537 - PubMed: Colombo-2020 - F no - - - - - - retinal disease - 1 1 LOVD
00424209 ? PubMed: Keen 2002 9-generation family, 47 affected individuals; segregation is a strong suggestion of causality, but there is doubt - the original His137Leu variant may be a paralogous variant (concurrent sequence from a gene and a pseudogene) and no additional mutations have been reported to segregate with disease M;F - United Kingdom (Great Britain) Southern English - - - - retinal disease - 1 1 LOVD
Legend   How to query  


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