TNFSF12:Ensemblv90

TNF superfamily member 12
OMIM: 602695, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red TNFSF12 in Mendeliome


Version 1.3802

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Inborn error of immunity, MONDO:0003778, TNFSF12-related

Red TNFSF12 in Predominantly Antibody Deficiency


Level 2: Immunological disorders
Version 1.4

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • 2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Inborn error of immunity, MONDO:0003778, TNFSF12-related

    Red TNFSF12 in Common Variable Immunodeficiency


    Level 2: Immunological disorders
    Version 1.15

    2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Inborn error of immunity, MONDO:0003778, TNFSF12-related