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Date	Panel	Item	Activity
Filter activities 9 actions
29 Feb 2020	Mendeliome v0.1525	SYT14	Zornitza Stark Marked gene: SYT14 as ready
29 Feb 2020	Mendeliome v0.1525	SYT14	Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
29 Feb 2020	Mendeliome v0.1525	SYT14	Zornitza Stark Phenotypes for gene: SYT14 were changed from to Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229
29 Feb 2020	Mendeliome v0.1524	SYT14	Zornitza Stark Publications for gene: SYT14 were set to
29 Feb 2020	Mendeliome v0.1523	SYT14	Zornitza Stark Mode of inheritance for gene: SYT14 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
29 Feb 2020	Mendeliome v0.1522	SYT14	Zornitza Stark Classified gene: SYT14 as Red List (low evidence)
29 Feb 2020	Mendeliome v0.1522	SYT14	Zornitza Stark Gene: syt14 has been classified as Red List (Low Evidence).
29 Feb 2020	Mendeliome v0.1521	SYT14	Zornitza Stark reviewed gene: SYT14: Rating: RED; Mode of pathogenicity: None; Publications: 21835308; Phenotypes: Spinocerebellar ataxia, autosomal recessive 11, MIM# 614229; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Nov 2019	Mendeliome v0.0	SYT14	Zornitza Stark gene: SYT14 was added gene: SYT14 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: SYT14 was set to Unknown