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Ataxia v2.0 VRK1 Gene migrated from ENSG00000100749 to ENSG00000100749 (gene set migration)
Ataxia v0.161 VRK1 Bryony Thompson Deleted their review
Ataxia v0.161 VRK1 Bryony Thompson Deleted their comment
Ataxia v0.58 VRK1 Zornitza Stark Marked gene: VRK1 as ready
Ataxia v0.58 VRK1 Zornitza Stark Gene: vrk1 has been classified as Amber List (Moderate Evidence).
Ataxia v0.58 VRK1 Zornitza Stark Publications for gene: VRK1 were set to
Ataxia v0.57 VRK1 Zornitza Stark Classified gene: VRK1 as Amber List (moderate evidence)
Ataxia v0.57 VRK1 Zornitza Stark Gene: vrk1 has been classified as Amber List (Moderate Evidence).
Ataxia v0.56 VRK1 Zornitza Stark reviewed gene: VRK1: Rating: AMBER; Mode of pathogenicity: None; Publications: 19646678, 21937992, 25609612, 24126608, 27281532; Phenotypes: Pontocerebellar hypoplasia type 1A, MIM# 607596; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Ataxia v0.46 VRK1 Bryony Thompson gene: VRK1 was added
gene: VRK1 was added to Ataxia - paediatric_RMH. Sources: Expert list
Mode of inheritance for gene: VRK1 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: VRK1 were set to Pontocerebellar hypoplasia type 1A, 607596
Review for gene: VRK1 was set to RED
Added comment: Ataxia can be a feature of the phenotype. Biallelic variants cause pontocerebellar hypoplasia and death before age 12, thus not a relevant gene for testing in an adult hospital.
Sources: Expert list