All individuals with variants in gene ZNF423

11 entries on 1 page. Showing entries 1 - 11.
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     
00019896 - PubMed: Gilissen 2014 - ? ? - - - - - - ID - 1 1 Marianne Vos (LOVD-team)
00144156 - PubMed: Katagiri 2014 index patient F no Japan Japanese - - - - retinal disease - 1 1 Rob W.J. Collin
00150185 26539891-FamBAB5590 PubMed: Karaca 2015 - - - - - - - family structure in paper - ? Macrocephaly, extended subarachnoid spaces, thin corpus callosum, hypopigmented fundus 2 2 Johan den Dunnen
00291474 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00291475 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 241 Mohammed Faruq
00291476 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 241 Mohammed Faruq
00304514 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 5 Mohammed Faruq
00304515 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 5 Mohammed Faruq
00375414 RP#006 PubMed: Katagiri 2014 family - - Japan - - - - - retinal disease see paper; ... 1 1 LOVD
00399832 369 PubMed: Tang 2022, Journal: Tang 2022 - - - China - - - - - NPHP - 1 1 Johan den Dunnen
00414440 WHP107 PubMed: Sun 2018 - M - China - - - - - ? - 2 1 LOVD
Legend   How to query  


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