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BabyScreen+ newborn screening v1.114 ALG6 Tommy Li Added phenotypes Congenital disorder of glycosylation, type Ic (MIM#603147) for gene: ALG6
BabyScreen+ newborn screening v0.169 ALG6 Zornitza Stark Marked gene: ALG6 as ready
BabyScreen+ newborn screening v0.169 ALG6 Zornitza Stark Gene: alg6 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.169 ALG6 Zornitza Stark Phenotypes for gene: ALG6 were changed from Congenital disorder of glycosylation, type Ic to Congenital disorder of glycosylation, type Ic (MIM#603147)
BabyScreen+ newborn screening v0.168 ALG6 Zornitza Stark Classified gene: ALG6 as Red List (low evidence)
BabyScreen+ newborn screening v0.168 ALG6 Zornitza Stark Gene: alg6 has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.167 ALG6 Zornitza Stark reviewed gene: ALG6: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type Ic (MIM#603147); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 ALG6 Zornitza Stark gene: ALG6 was added
gene: ALG6 was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: ALG6 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: ALG6 were set to Congenital disorder of glycosylation, type Ic