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Date	Panel	Item	Activity
Filter activities 7 actions
10 Apr 2020	Complement Deficiencies v0.21	CFHR4	Zornitza Stark Marked gene: CFHR4 as ready
10 Apr 2020	Complement Deficiencies v0.21	CFHR4	Zornitza Stark Gene: cfhr4 has been classified as Red List (Low Evidence).
10 Apr 2020	Complement Deficiencies v0.21	CFHR4	Zornitza Stark Classified gene: CFHR4 as Red List (low evidence)
10 Apr 2020	Complement Deficiencies v0.21	CFHR4	Zornitza Stark Gene: cfhr4 has been classified as Red List (Low Evidence).
10 Apr 2020	Complement Deficiencies v0.20	CFHR4	Zornitza Stark changed review comment from: Association is with aHUS, gene is on aHUS panel.; to: No Mendelian gene disease association I can find.
10 Apr 2020	Complement Deficiencies v0.20	CFHR4	Zornitza Stark reviewed gene: CFHR4: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Susceptibility to atypical haemolytic uraemic syndrome; Mode of inheritance: None
17 Nov 2019	Complement Deficiencies v0.0	CFHR4	Zornitza Stark gene: CFHR4 was added gene: CFHR4 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: CFHR4 was set to Unknown