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Date	Panel	Item	Activity
Filter activities 7 actions
20 Oct 2022	BabyScreen+ newborn screening v0.595	VPS13B	Zornitza Stark Marked gene: VPS13B as ready
20 Oct 2022	BabyScreen+ newborn screening v0.595	VPS13B	Zornitza Stark Gene: vps13b has been classified as Red List (Low Evidence).
20 Oct 2022	BabyScreen+ newborn screening v0.595	VPS13B	Zornitza Stark Phenotypes for gene: VPS13B were changed from Cohen syndrome to Cohen syndrome MIM#216550
20 Oct 2022	BabyScreen+ newborn screening v0.594	VPS13B	Zornitza Stark Classified gene: VPS13B as Red List (low evidence)
20 Oct 2022	BabyScreen+ newborn screening v0.594	VPS13B	Zornitza Stark Gene: vps13b has been classified as Red List (Low Evidence).
20 Oct 2022	BabyScreen+ newborn screening v0.588	VPS13B	Lilian Downie reviewed gene: VPS13B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Cohen syndrome MIM#216550; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	VPS13B	Zornitza Stark gene: VPS13B was added gene: VPS13B was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: VPS13B was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: VPS13B were set to Cohen syndrome