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Date	Panel	Item	Activity
Filter activities 8 actions
30 Jan 2020	Mendeliome v0.1048	CACNG2	Zornitza Stark Marked gene: CACNG2 as ready
30 Jan 2020	Mendeliome v0.1048	CACNG2	Zornitza Stark Gene: cacng2 has been classified as Red List (Low Evidence).
30 Jan 2020	Mendeliome v0.1048	CACNG2	Zornitza Stark Phenotypes for gene: CACNG2 were changed from to Mental retardation, autosomal dominant 10, MIM#614256
30 Jan 2020	Mendeliome v0.1047	CACNG2	Zornitza Stark Publications for gene: CACNG2 were set to
30 Jan 2020	Mendeliome v0.1046	CACNG2	Zornitza Stark Classified gene: CACNG2 as Red List (low evidence)
30 Jan 2020	Mendeliome v0.1046	CACNG2	Zornitza Stark Gene: cacng2 has been classified as Red List (Low Evidence).
30 Jan 2020	Mendeliome v0.1045	CACNG2	Zornitza Stark reviewed gene: CACNG2: Rating: RED; Mode of pathogenicity: None; Publications: 21376300; Phenotypes: Mental retardation, autosomal dominant 10, MIM#614256; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
17 Nov 2019	Mendeliome v0.0	CACNG2	Zornitza Stark gene: CACNG2 was added gene: CACNG2 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CACNG2 was set to Unknown