NFAT5

nuclear factor of activated T-cells 5
OMIM: 604708, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber NFAT5 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Immune deficiency disease, MONDO:0003778, NFAT5-related
  • Recurrent infections
  • Autoimmune enterocolopathy
  • EBV susceptibility
  • HLH

Amber NFAT5 in Disorders of immune dysregulation


Level 2: Immunological disorders
Version 0.186

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immune deficiency disease, MONDO:0003778, NFAT5-related
    • Recurrent infections
    • Autoimmune enterocolopathy
    • EBV susceptibility
    • HLH