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Complement Deficiencies v0.86 CFHR5 Bryony Thompson Mode of inheritance for gene: CFHR5 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Complement Deficiencies v0.85 CFHR5 Bryony Thompson Classified gene: CFHR5 as Green List (high evidence)
Complement Deficiencies v0.85 CFHR5 Bryony Thompson Added comment: Comment on list classification: IUIS include this gene on their July 2024 list of inborn errors of immunology
Complement Deficiencies v0.85 CFHR5 Bryony Thompson Gene: cfhr5 has been classified as Green List (High Evidence).
Complement Deficiencies v0.23 CFHR5 Zornitza Stark Marked gene: CFHR5 as ready
Complement Deficiencies v0.23 CFHR5 Zornitza Stark Gene: cfhr5 has been classified as Red List (Low Evidence).
Complement Deficiencies v0.23 CFHR5 Zornitza Stark Phenotypes for gene: CFHR5 were changed from to Nephropathy due to CFHR5 deficiency, MIM# 614809
Complement Deficiencies v0.22 CFHR5 Zornitza Stark Classified gene: CFHR5 as Red List (low evidence)
Complement Deficiencies v0.22 CFHR5 Zornitza Stark Gene: cfhr5 has been classified as Red List (Low Evidence).
Complement Deficiencies v0.21 CFHR5 Zornitza Stark reviewed gene: CFHR5: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Nephropathy due to CFHR5 deficiency, MIM# 614809; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Complement Deficiencies v0.0 CFHR5 Zornitza Stark gene: CFHR5 was added
gene: CFHR5 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: CFHR5 was set to Unknown