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Date	Panel	Item	Activity
Filter activities 7 actions
23 Sep 2022	BabyScreen+ newborn screening v0.167	ALG3	Zornitza Stark Marked gene: ALG3 as ready
23 Sep 2022	BabyScreen+ newborn screening v0.167	ALG3	Zornitza Stark Gene: alg3 has been classified as Red List (Low Evidence).
23 Sep 2022	BabyScreen+ newborn screening v0.167	ALG3	Zornitza Stark Phenotypes for gene: ALG3 were changed from Congenital disorder of glycosylation, type Id to Congenital disorder of glycosylation, type Id, MIM# 601110
23 Sep 2022	BabyScreen+ newborn screening v0.166	ALG3	Zornitza Stark Classified gene: ALG3 as Red List (low evidence)
23 Sep 2022	BabyScreen+ newborn screening v0.166	ALG3	Zornitza Stark Gene: alg3 has been classified as Red List (Low Evidence).
23 Sep 2022	BabyScreen+ newborn screening v0.165	ALG3	Zornitza Stark reviewed gene: ALG3: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type Id 601110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Sep 2022	BabyScreen+ newborn screening v0.0	ALG3	Zornitza Stark gene: ALG3 was added gene: ALG3 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green Mode of inheritance for gene: ALG3 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ALG3 were set to Congenital disorder of glycosylation, type Id