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Date	Panel	Item	Activity
Filter activities 9 actions
10 Apr 2020	Mendeliome v0.2083	FCN3	Zornitza Stark Marked gene: FCN3 as ready
10 Apr 2020	Mendeliome v0.2083	FCN3	Zornitza Stark Gene: fcn3 has been classified as Amber List (Moderate Evidence).
10 Apr 2020	Mendeliome v0.2083	FCN3	Zornitza Stark Phenotypes for gene: FCN3 were changed from to Immunodeficiency due to ficolin 3 deficiency, MIM# 613860
10 Apr 2020	Mendeliome v0.2082	FCN3	Zornitza Stark Publications for gene: FCN3 were set to
10 Apr 2020	Mendeliome v0.2081	FCN3	Zornitza Stark Mode of inheritance for gene: FCN3 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
10 Apr 2020	Mendeliome v0.2080	FCN3	Zornitza Stark Classified gene: FCN3 as Amber List (moderate evidence)
10 Apr 2020	Mendeliome v0.2080	FCN3	Zornitza Stark Gene: fcn3 has been classified as Amber List (Moderate Evidence).
10 Apr 2020	Mendeliome v0.2079	FCN3	Zornitza Stark reviewed gene: FCN3: Rating: AMBER; Mode of pathogenicity: None; Publications: 25662573, 22226667, 19535802, 20971976; Phenotypes: Immunodeficiency due to ficolin 3 deficiency, MIM# 613860; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Nov 2019	Mendeliome v0.0	FCN3	Zornitza Stark gene: FCN3 was added gene: FCN3 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: FCN3 was set to Unknown