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Congenital nystagmus v0.162 DGUOK Zornitza Stark Marked gene: DGUOK as ready
Congenital nystagmus v0.162 DGUOK Zornitza Stark Gene: dguok has been classified as Red List (Low Evidence).
Congenital nystagmus v0.162 DGUOK Zornitza Stark Phenotypes for gene: DGUOK were changed from Mitochondrial DNA depletion syndrome 3 to Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), MIM# 251880
Congenital nystagmus v0.161 DGUOK Zornitza Stark reviewed gene: DGUOK: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), MIM# 251880; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Congenital nystagmus v0.4 DGUOK Zornitza Stark Added phenotypes Mitochondrial DNA depletion syndrome 3 for gene: DGUOK
Congenital nystagmus v0.0 DGUOK Zornitza Stark gene: DGUOK was added
gene: DGUOK was added to Albinism or congenital nystagmus. Sources: Expert Review Red,NHS Genomic Medicine Service,Genomics England PanelApp
Mode of inheritance for gene: DGUOK was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: DGUOK were set to 12210798; 12205643
Phenotypes for gene: DGUOK were set to Mitochondrial DNA depletion syndrome 3