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Date	Panel	Item	Activity
Filter activities 7 actions
23 Sep 2022	BabyScreen+ newborn screening v0.156	B3GLCT	Zornitza Stark Marked gene: B3GLCT as ready
23 Sep 2022	BabyScreen+ newborn screening v0.156	B3GLCT	Zornitza Stark Gene: b3glct has been classified as Red List (Low Evidence).
23 Sep 2022	BabyScreen+ newborn screening v0.156	B3GLCT	Zornitza Stark Phenotypes for gene: B3GLCT were changed from Peters-Plus syndrome to Peters-plus syndrome, MIM#261540
23 Sep 2022	BabyScreen+ newborn screening v0.155	B3GLCT	Zornitza Stark Classified gene: B3GLCT as Red List (low evidence)
23 Sep 2022	BabyScreen+ newborn screening v0.155	B3GLCT	Zornitza Stark Gene: b3glct has been classified as Red List (Low Evidence).
23 Sep 2022	BabyScreen+ newborn screening v0.154	B3GLCT	Zornitza Stark reviewed gene: B3GLCT: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Peters-plus syndrome, MIM#261540; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	B3GLCT	Zornitza Stark gene: B3GLCT was added gene: B3GLCT was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: B3GLCT was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: B3GLCT were set to Peters-Plus syndrome