IRF7

interferon regulatory factor 7
OMIM: 605047, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Red IRF7 in Genomic imprinting Version 0.149	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 1.3	review	Not set	Sources Literature
Green IRF7 in COVID-19 research Level 2: Viral research Version 1.141	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
Green IRF7 in Primary immunodeficiency or monogenic inflammatory bowel disease Version 4.197 Latest signed off version: v4.0 (22 Mar 2023)	review	BIALLELIC, autosomal or pseudoautosomal	Sources NHS GMS Expert Review Green IUIS Classification December 2019 IUIS Classification February 2018 Victorian Clinical Genetics Services GRID V2.0 Phenotypes Immunodeficiency 39 , OMIM:616345
Amber IRF7 in Severe Paediatric Disorders Version 1.184	review	BIALLELIC, autosomal or pseudoautosomal	Sources Next Generation Children Project Expert Review Amber Expert list Phenotypes ?Immunodeficiency 39, 616345