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Mitochondrial disease v0.198 CEP89 Zornitza Stark edited their review of gene: CEP89: Changed rating: RED
Mitochondrial disease v0.7 CEP89 Zornitza Stark Marked gene: CEP89 as ready
Mitochondrial disease v0.7 CEP89 Zornitza Stark Gene: cep89 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.7 CEP89 Zornitza Stark Phenotypes for gene: CEP89 were changed from to Mitochondrial complex IV deficiency
Mitochondrial disease v0.6 CEP89 Zornitza Stark Publications for gene: CEP89 were set to
Mitochondrial disease v0.5 CEP89 Zornitza Stark Mode of inheritance for gene: CEP89 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.4 CEP89 Zornitza Stark Classified gene: CEP89 as Amber List (moderate evidence)
Mitochondrial disease v0.4 CEP89 Zornitza Stark Gene: cep89 has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.3 CEP89 Zornitza Stark reviewed gene: CEP89: Rating: AMBER; Mode of pathogenicity: None; Publications: 23575228; Phenotypes: Mitochondrial complex IV deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.0 CEP89 Zornitza Stark gene: CEP89 was added
gene: CEP89 was added to Mitochondrial_AGHA_VCGS. Sources: Expert Review Green,Australian Genomics Health Alliance Mitochondrial Flagship,Victorian Clinical Genetics Services
Mode of inheritance for gene: CEP89 was set to Unknown