Activity

Filter

Cancel
Date Panel Item Activity
9 actions
Muscular dystrophy and myopathy_Paediatric v0.59 DPM2 Zornitza Stark Marked gene: DPM2 as ready
Muscular dystrophy and myopathy_Paediatric v0.59 DPM2 Zornitza Stark Gene: dpm2 has been classified as Amber List (Moderate Evidence).
Muscular dystrophy and myopathy_Paediatric v0.59 DPM2 Zornitza Stark Phenotypes for gene: DPM2 were changed from to Congenital disorder of glycosylation, type Iu, MIM# 615042
Muscular dystrophy and myopathy_Paediatric v0.58 DPM2 Zornitza Stark Publications for gene: DPM2 were set to
Muscular dystrophy and myopathy_Paediatric v0.57 DPM2 Zornitza Stark Mode of inheritance for gene: DPM2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Muscular dystrophy and myopathy_Paediatric v0.56 DPM2 Zornitza Stark Classified gene: DPM2 as Amber List (moderate evidence)
Muscular dystrophy and myopathy_Paediatric v0.56 DPM2 Zornitza Stark Gene: dpm2 has been classified as Amber List (Moderate Evidence).
Muscular dystrophy and myopathy_Paediatric v0.55 DPM2 Zornitza Stark reviewed gene: DPM2: Rating: AMBER; Mode of pathogenicity: None; Publications: 23109149; Phenotypes: Congenital disorder of glycosylation, type Iu, MIM# 615042; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Muscular dystrophy and myopathy_Paediatric v0.0 DPM2 Zornitza Stark gene: DPM2 was added
gene: DPM2 was added to Muscular dystrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: DPM2 was set to Unknown