All individuals with variants in gene WNT10B

8 entries on 1 page. Showing entries 1 - 8.
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     
00231002 32-II-1 - - F no Japan - - - - - SHFM6 split hand, split foot, syndactyly 2 2 Kaori Yamoto
00231003 33-II-1 - - F no Japan - - - - - SHFM6 split hand, syndactyly 1 1 Kaori Yamoto
00231004 34-II-1 - - M no Japan - - - - - SHFM6 split foot, ventricular septal defect 1 1 Kaori Yamoto
00231005 35-II-1 - - M no Japan - - - - - SHFM6 split foot, polydactyly, Microphthalmia, cryptorchidism, global developmental delay 1 1 Kaori Yamoto
00235305 32-II-2 - - M no Japan - - - - - SHFM6 split hand, syndactyly 2 1 Kaori Yamoto
00235401 Pat48 PubMed: Nagata 2014 - - yes Japan - - - - - SHFM split-hand/foot malformation 1 1 Johan den Dunnen
00290716 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00438716 HSJ0781 PubMed: Hamdan 2017 WGS analysis 197 individuals with unexplained DEE (unaffected parents) - - Canada - - - - pharmaco-resistant seizures DEE - 1 1 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.