IFNGR1

interferon gamma receptor 1
OMIM: 107470, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green IFNGR1 in Mendeliome


Version 1.2374

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Immunodeficiency 27A, mycobacteriosis, AR, MIM# 209950
  • Immunodeficiency 27B, mycobacteriosis, AD, MIM# 615978

Green IFNGR1 in Defects of intrinsic and innate immunity


Level 2: Immunological disorders
Version 1.20

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immunodeficiency 27A, mycobacteriosis, AR, MIM# 209950
    • Immunodeficiency 27B, mycobacteriosis, AD, MIM# 615978

    Green IFNGR1 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Immunodeficiency 27A, mycobacteriosis, AR, 209950 (3)

    Green IFNGR1 in Prepair 1000+


    Level 2: Screening
    Version 1.1586

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Immunodeficiency 27A, mycobacteriosis, AR, 209950 (3)

    Amber IFNGR1 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.116

    review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Immunodeficiency 27A, mycobacteriosis, AR, MIM# 209950
    • Immunodeficiency 27B, mycobacteriosis, AD, MIM# 615978
    Tags
    • treatable
    • immunological