ISG15

ISG15 ubiquitin-like modifier
OMIM: 147571, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green ISG15 in Brain Calcification


Level 2: Neurology and neurodevelopmental disorders
Version 1.99

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Immunodeficiency 38 with BG calcification, MIM# 616126

    Green ISG15 in Mendeliome


    Version 1.2374

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immunodeficiency 38, MIM# 616126

    Green ISG15 in Defects of intrinsic and innate immunity


    Level 2: Immunological disorders
    Version 1.20

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immunodeficiency 38, MIM# 616126