Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Cardiomyopathy_Paediatric v1.104 GBE1 Zornitza Stark Marked gene: GBE1 as ready
Cardiomyopathy_Paediatric v1.104 GBE1 Zornitza Stark Gene: gbe1 has been classified as Green List (High Evidence).
Cardiomyopathy_Paediatric v1.104 GBE1 Zornitza Stark Phenotypes for gene: GBE1 were changed from Glycogen Storage Disorders- Liver; Glycogen Storage Disorders- Muscle; Glycogen storage disease type IV, Andersen (Glycogen storage disorders); Glycogen storage disease IV, 232500; hypotonia, exercise intolerance, polyglucosan bodies in affected tissues; Glycogen Storage Disease Type IV; failure to thrive in addition to hepatomegaly van have neuromuscular adult form ( polyglucosan body ideas which presents with neurogenic bladder, gait difficulties; DCM; Polyglucosan body disease, adult form, 263570; Glycogen storage disease type IV (brancher enzyme deficiency), neuromuscular form; Hypertrophic-hypocontractile cardiomyopathy; Glycogen Storage Disease to glycogen storage disease due to glycogen branching enzyme deficiency, MONDO:0009292
Cardiomyopathy_Paediatric v1.103 GBE1 Zornitza Stark Classified gene: GBE1 as Green List (high evidence)
Cardiomyopathy_Paediatric v1.103 GBE1 Zornitza Stark Gene: gbe1 has been classified as Green List (High Evidence).
Cardiomyopathy_Paediatric v1.102 GBE1 Zornitza Stark reviewed gene: GBE1: Rating: GREEN; Mode of pathogenicity: None; Publications: 38516405, 38436530, 38012812, 36830903, 29379554; Phenotypes: glycogen storage disease due to glycogen branching enzyme deficiency, MONDO:0009292; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cardiomyopathy_Paediatric v1.0 GBE1 Gene migrated from ENSG00000114480 to ENSG00000114480 (gene set migration)
Cardiomyopathy_Paediatric v0.0 GBE1 Zornitza Stark gene: GBE1 was added
gene: GBE1 was added to Cardiomyopathy_Paediatric. Sources: NHS GMS,Expert Review Red,South West GLH,MetBioNet
Mode of inheritance for gene: GBE1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GBE1 were set to 27604308
Phenotypes for gene: GBE1 were set to Glycogen Storage Disorders- Liver; Glycogen Storage Disorders- Muscle; Glycogen storage disease type IV, Andersen (Glycogen storage disorders); Glycogen storage disease IV, 232500; hypotonia, exercise intolerance, polyglucosan bodies in affected tissues; Glycogen Storage Disease Type IV; failure to thrive in addition to hepatomegaly van have neuromuscular adult form ( polyglucosan body ideas which presents with neurogenic bladder, gait difficulties; DCM; Polyglucosan body disease, adult form, 263570; Glycogen storage disease type IV (brancher enzyme deficiency), neuromuscular form; Hypertrophic-hypocontractile cardiomyopathy; Glycogen Storage Disease