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Date	Panel	Item	Activity
Filter activities 6 actions
25 Oct 2021	Congenital nystagmus v0.44	GRK1	Zornitza Stark Marked gene: GRK1 as ready
25 Oct 2021	Congenital nystagmus v0.44	GRK1	Zornitza Stark Gene: grk1 has been classified as Red List (Low Evidence).
25 Oct 2021	Congenital nystagmus v0.44	GRK1	Zornitza Stark Classified gene: GRK1 as Red List (low evidence)
25 Oct 2021	Congenital nystagmus v0.44	GRK1	Zornitza Stark Gene: grk1 has been classified as Red List (Low Evidence).
25 Oct 2021	Congenital nystagmus v0.43	GRK1	Zornitza Stark reviewed gene: GRK1: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Oguchi disease-2, MIM# 613411; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
06 Oct 2021	Congenital nystagmus v0.4	GRK1	Zornitza Stark gene: GRK1 was added gene: GRK1 was added to Congenital nystagmus. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: GRK1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: GRK1 were set to Oguchi disease-2, 613411