Activity

Filter

Panel

Version

Gene or Genomic Entity Name

Date from

Date to

Cancel

Date	Panel	Item	Activity
Filter activities 9 actions
22 Jul 2020	Congenital Disorders of Glycosylation v0.135	COG2	Zornitza Stark Marked gene: COG2 as ready
22 Jul 2020	Congenital Disorders of Glycosylation v0.135	COG2	Zornitza Stark Gene: cog2 has been classified as Red List (Low Evidence).
22 Jul 2020	Congenital Disorders of Glycosylation v0.135	COG2	Zornitza Stark Phenotypes for gene: COG2 were changed from to Congenital disorder of glycosylation, type IIq (MIM# 617395)
22 Jul 2020	Congenital Disorders of Glycosylation v0.134	COG2	Zornitza Stark Publications for gene: COG2 were set to
22 Jul 2020	Congenital Disorders of Glycosylation v0.133	COG2	Zornitza Stark Mode of inheritance for gene: COG2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
22 Jul 2020	Congenital Disorders of Glycosylation v0.132	COG2	Zornitza Stark Classified gene: COG2 as Red List (low evidence)
22 Jul 2020	Congenital Disorders of Glycosylation v0.132	COG2	Zornitza Stark Gene: cog2 has been classified as Red List (Low Evidence).
22 Jul 2020	Congenital Disorders of Glycosylation v0.131	COG2	Ain Roesley reviewed gene: COG2: Rating: RED; Mode of pathogenicity: None; Publications: 24784932; Phenotypes: Congenital disorder of glycosylation, type IIq (MIM# 617395); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
17 Nov 2019	Congenital Disorders of Glycosylation v0.0	COG2	Zornitza Stark gene: COG2 was added gene: COG2 was added to Congenital Disorders of Glycosylation_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: COG2 was set to Unknown