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Congenital Disorders of Glycosylation v2.0 CHST8 Gene migrated from ENSG00000124302 to ENSG00000124302 (gene set migration)
Congenital Disorders of Glycosylation v0.33 CHST8 Zornitza Stark Marked gene: CHST8 as ready
Congenital Disorders of Glycosylation v0.33 CHST8 Zornitza Stark Gene: chst8 has been classified as Red List (Low Evidence).
Congenital Disorders of Glycosylation v0.33 CHST8 Zornitza Stark Phenotypes for gene: CHST8 were changed from to Peeling Skin Syndrome
Congenital Disorders of Glycosylation v0.32 CHST8 Zornitza Stark Publications for gene: CHST8 were set to
Congenital Disorders of Glycosylation v0.31 CHST8 Zornitza Stark Mode of inheritance for gene: CHST8 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.30 CHST8 Zornitza Stark Classified gene: CHST8 as Red List (low evidence)
Congenital Disorders of Glycosylation v0.30 CHST8 Zornitza Stark Gene: chst8 has been classified as Red List (Low Evidence).
Congenital Disorders of Glycosylation v0.29 CHST8 Elena Savva reviewed gene: CHST8: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 22289416, 28204496; Phenotypes: Peeling Skin Syndrome; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital Disorders of Glycosylation v0.0 CHST8 Zornitza Stark gene: CHST8 was added
gene: CHST8 was added to Congenital Disorders of Glycosylation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CHST8 was set to Unknown