IRF7

interferon regulatory factor 7
OMIM: 605047, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red IRF7 in Genomic imprinting


Version 0.104

review MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • Literature

Red IRF7 in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.1

review Not set
Sources
  • Literature

Green IRF7 in COVID-19 research


Level 2: Viral research
Version 1.77

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • Melbourne Genomics Health Alliance Immunology Flagship
  • IUIS Classification December 2019
  • IUIS Classification February 2018
  • Victorian Clinical Genetics Services
  • GRID V2.0
  • Literature
Phenotypes
  • Severe influenza
  • ?Immunodeficiency 39, 616345
  • Severe influenza disease
  • IRF7 deficiency
  • Defects in Intrinsic and Innate Immunity

Amber IRF7 in Primary immunodeficiency


Version 2.427
Latest signed off version: v2.1 (24 Feb 2020)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • IUIS Classification December 2019
  • IUIS Classification February 2018
  • Victorian Clinical Genetics Services
  • Expert Review Amber
  • GRID V2.0
Phenotypes
  • Severe influenza
  • Defects in Intrinsic and Innate Immunity
  • IRF7 deficiency
  • ?Immunodeficiency 39, 616345
  • Severe influenza disease

Amber IRF7 in Severe Paediatric Disorders


Version 1.78

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Next Generation Children Project
  • Expert Review Amber
  • Expert list
Phenotypes
  • ?Immunodeficiency 39, 616345