All individuals with variants in gene GNPAT

14 entries on 1 page. Showing entries 1 - 14.
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AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00245706 - - - - - - - - - - - Healthy/Control - 2 1 LOVD
00245707 - - 2-generation family, 3 affecteds (2M, F) - yes - - - - - - RCDP2 - 1 3 LOVD
00245708 - - - - - - - - - - - RCDP2 - 1 1 LOVD
00245709 - - - - - - - - - - - RCDP2 - 1 1 LOVD
00245710 - - - - - - - - - - - RCDP2 - 1 1 LOVD
00245711 - - - - - - - - - - - RCDP2 - 1 1 LOVD
00245712 - - - - - - - - - - - RCDP2 - 1 1 LOVD
00245713 - - - - - - - - - - - ? - 2 1 Brandon Itzkovitz
00245714 - - - M - - - - - - - RCDP2 - 1 1 Brandon Itzkovitz
00245715 - - - M - - - - - - - RCDP2 - 1 1 Brandon Itzkovitz
00245716 - - - - - - - - - - - RCDP2 Less severe 1 1 Brandon Itzkovitz
00331463 DG08RC00021 PubMed: Maddirevula 2018 family F yes - Arab - - - - skeletal dysplasia Global developmental delay, Microcephaly, Anteverted nares, Brachycephaly, Optic disc p Yes 1 1 LOVD
00391876 133P - - M no Spain - - - - - CPDX1 - 2 1 Alejandro Brea-Fernández
00444981 14DG2068 PubMed: Patel 2017 simplex case - - - - - - - - CTRCT cataract as part of rhizomelic chondrodysplasia punctata; syndromic 1 2 Johan den Dunnen
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