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Congenital Disorders of Glycosylation v2.0 POGLUT1 Gene migrated from ENSG00000163389 to ENSG00000163389 (gene set migration)
Congenital Disorders of Glycosylation v0.126 POGLUT1 Zornitza Stark Marked gene: POGLUT1 as ready
Congenital Disorders of Glycosylation v0.126 POGLUT1 Zornitza Stark Added comment: Comment when marking as ready: Limited evidence for bi-allelic disease or for CDG association.
Congenital Disorders of Glycosylation v0.126 POGLUT1 Zornitza Stark Gene: poglut1 has been classified as Red List (Low Evidence).
Congenital Disorders of Glycosylation v0.126 POGLUT1 Zornitza Stark Phenotypes for gene: POGLUT1 were changed from to Muscular dystrophy, limb-girdle, autosomal recessive 21 (MIM# 617232), Dowling-Degos disease 4 (MIM# 615696)
Congenital Disorders of Glycosylation v0.125 POGLUT1 Zornitza Stark Mode of inheritance for gene: POGLUT1 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to BIALLELIC, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.124 POGLUT1 Zornitza Stark Publications for gene: POGLUT1 were set to
Congenital Disorders of Glycosylation v0.123 POGLUT1 Zornitza Stark Mode of inheritance for gene: POGLUT1 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Congenital Disorders of Glycosylation v0.121 POGLUT1 Zornitza Stark Classified gene: POGLUT1 as Red List (low evidence)
Congenital Disorders of Glycosylation v0.121 POGLUT1 Zornitza Stark Gene: poglut1 has been classified as Red List (Low Evidence).
Congenital Disorders of Glycosylation v0.120 POGLUT1 Zornitza Stark Mode of inheritance for gene: POGLUT1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.119 POGLUT1 Zornitza Stark Classified gene: POGLUT1 as Amber List (moderate evidence)
Congenital Disorders of Glycosylation v0.119 POGLUT1 Zornitza Stark Gene: poglut1 has been classified as Amber List (Moderate Evidence).
Congenital Disorders of Glycosylation v0.96 POGLUT1 Ain Roesley reviewed gene: POGLUT1: Rating: AMBER; Mode of pathogenicity: None; Publications: 27807076, 24387993; Phenotypes: Muscular dystrophy, limb-girdle, autosomal recessive 21 (MIM# 617232), Dowling-Degos disease 4 (MIM# 615696); Mode of inheritance: Other
Congenital Disorders of Glycosylation v0.0 POGLUT1 Zornitza Stark gene: POGLUT1 was added
gene: POGLUT1 was added to Congenital Disorders of Glycosylation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: POGLUT1 was set to Unknown