PLCG2

phospholipase C gamma 2
OMIM: 600220, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green PLCG2 in Vasculitis


Level 2: Immunological disorders
Version 0.82

review Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Red PLCG2 in Cataract


Level 2: Ophthalmological disorders
Version 0.366

review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services

Green PLCG2 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
  • Victorian Clinical Genetics Services
Phenotypes
  • Common variable immunodeficiency
  • Autoinflammation, antibody deficiency, and immune dysregulation syndrome MIM#614878

Green PLCG2 in Common Variable Immunodeficiency


Level 2: Immunological disorders
Version 1.12

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Common variable immunodeficiency
    • Autoinflammation, antibody deficiency, and immune dysregulation syndrome MIM#614878

    Green PLCG2 in Susceptibility to Viral Infections


    Level 2: Immunological disorders
    Version 0.117

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Hereditary susceptibility to infections, MONDO:0015979, PLCG2-related
    • Susceptibility to herpes virus

    Green PLCG2 in Systemic Autoinflammatory Disease_Periodic Fever


    Level 2: Immunological disorders
    Version 1.47

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Autoinflammation, antibody deficiency, and immune dysregulation syndrome MIM#614878