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Complement Deficiencies v0.81 CFHR1 Bryony Thompson Publications for gene: CFHR1 were set to
Complement Deficiencies v0.80 CFHR1 Bryony Thompson Mode of inheritance for gene: CFHR1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Complement Deficiencies v0.79 CFHR1 Bryony Thompson Classified gene: CFHR1 as Green List (high evidence)
Complement Deficiencies v0.79 CFHR1 Bryony Thompson Added comment: Comment on list classification: IUIS include this gene on their July 2024 list of inborn errors of immunology
Complement Deficiencies v0.79 CFHR1 Bryony Thompson Gene: cfhr1 has been classified as Green List (High Evidence).
Complement Deficiencies v0.13 CFHR1 Zornitza Stark Marked gene: CFHR1 as ready
Complement Deficiencies v0.13 CFHR1 Zornitza Stark Gene: cfhr1 has been classified as Red List (Low Evidence).
Complement Deficiencies v0.13 CFHR1 Zornitza Stark Classified gene: CFHR1 as Red List (low evidence)
Complement Deficiencies v0.13 CFHR1 Zornitza Stark Gene: cfhr1 has been classified as Red List (Low Evidence).
Complement Deficiencies v0.12 CFHR1 Zornitza Stark reviewed gene: CFHR1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Complement Deficiencies v0.0 CFHR1 Zornitza Stark gene: CFHR1 was added
gene: CFHR1 was added to Complement deficiencies_MGHA_AGHA_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship
Mode of inheritance for gene: CFHR1 was set to Unknown