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Combined Immunodeficiency v2.0 IRF4 Gene migrated from ENSG00000137265 to ENSG00000137265 (gene set migration)
Combined Immunodeficiency v1.115 IRF4 Zornitza Stark Phenotypes for gene: IRF4 were changed from Combined immunodeficiency, MONDO:0015131, IRF4-related to Immunodeficiency 131, MIM# 621097
Combined Immunodeficiency v1.48 IRF4 Zornitza Stark Phenotypes for gene: IRF4 were changed from Combined immunodeficiency to Combined immunodeficiency, MONDO:0015131, IRF4-related
Combined Immunodeficiency v1.47 IRF4 Zornitza Stark Publications for gene: IRF4 were set to 29408330
Combined Immunodeficiency v1.46 IRF4 Zornitza Stark Mode of inheritance for gene: IRF4 was changed from BIALLELIC, autosomal or pseudoautosomal to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Combined Immunodeficiency v1.45 IRF4 Zornitza Stark Classified gene: IRF4 as Green List (high evidence)
Combined Immunodeficiency v1.45 IRF4 Zornitza Stark Gene: irf4 has been classified as Green List (High Evidence).
Combined Immunodeficiency v1.44 IRF4 Peter McNaughton reviewed gene: IRF4: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 36662884; Phenotypes: Combined Immune deficiency; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Combined Immunodeficiency v0.176 IRF4 Bryony Thompson Marked gene: IRF4 as ready
Combined Immunodeficiency v0.176 IRF4 Bryony Thompson Gene: irf4 has been classified as Amber List (Moderate Evidence).
Combined Immunodeficiency v0.176 IRF4 Bryony Thompson Classified gene: IRF4 as Amber List (moderate evidence)
Combined Immunodeficiency v0.176 IRF4 Bryony Thompson Gene: irf4 has been classified as Amber List (Moderate Evidence).
Combined Immunodeficiency v0.175 IRF4 Bryony Thompson gene: IRF4 was added
gene: IRF4 was added to Combined Immunodeficiency. Sources: Other
Mode of inheritance for gene: IRF4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: IRF4 were set to 29408330
Phenotypes for gene: IRF4 were set to Combined immunodeficiency
Review for gene: IRF4 was set to AMBER
Added comment: A single case with a homozygous splice variant inherited by uniparental isodisomy, and previously reported supporting null animal models.
Sources: Other