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Congenital nystagmus v2.0 RGS9 Gene migrated from ENSG00000108370 to ENSG00000108370 (gene set migration)
Congenital nystagmus v1.9 RGS9 Bryony Thompson Deleted their review
Congenital nystagmus v0.127 RGS9BP Zornitza Stark Marked gene: RGS9BP as ready
Congenital nystagmus v0.127 RGS9BP Zornitza Stark Gene: rgs9bp has been classified as Red List (Low Evidence).
Congenital nystagmus v0.127 RGS9BP Zornitza Stark Classified gene: RGS9BP as Red List (low evidence)
Congenital nystagmus v0.127 RGS9BP Zornitza Stark Gene: rgs9bp has been classified as Red List (Low Evidence).
Congenital nystagmus v0.126 RGS9BP Zornitza Stark reviewed gene: RGS9BP: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Bradyopsia MIM#608415; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital nystagmus v0.126 RGS9 Zornitza Stark Marked gene: RGS9 as ready
Congenital nystagmus v0.126 RGS9 Zornitza Stark Gene: rgs9 has been classified as Red List (Low Evidence).
Congenital nystagmus v0.126 RGS9 Zornitza Stark Classified gene: RGS9 as Red List (low evidence)
Congenital nystagmus v0.126 RGS9 Zornitza Stark Gene: rgs9 has been classified as Red List (Low Evidence).
Congenital nystagmus v0.125 RGS9 Zornitza Stark reviewed gene: RGS9: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Bradyopsia MIM#608415; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital nystagmus v0.4 RGS9BP Zornitza Stark gene: RGS9BP was added
gene: RGS9BP was added to Congenital nystagmus. Sources: Expert Review Green,Expert list
Mode of inheritance for gene: RGS9BP was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RGS9BP were set to 19818506; 14702087
Phenotypes for gene: RGS9BP were set to Bradyopsia MIM#608415
Congenital nystagmus v0.4 RGS9 Zornitza Stark gene: RGS9 was added
gene: RGS9 was added to Congenital nystagmus. Sources: Expert Review Green,Expert list
Mode of inheritance for gene: RGS9 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: RGS9 were set to 10676965; 29107794; 14702087
Phenotypes for gene: RGS9 were set to Bradyopsia MIM#608415