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Intellectual disability syndromic and non-syndromic v0.788 CEP89 Zornitza Stark Marked gene: CEP89 as ready
Intellectual disability syndromic and non-syndromic v0.788 CEP89 Zornitza Stark Gene: cep89 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.788 CEP89 Zornitza Stark Phenotypes for gene: CEP89 were changed from to Mitochondrial complex IV deficiency
Intellectual disability syndromic and non-syndromic v0.787 CEP89 Zornitza Stark Publications for gene: CEP89 were set to
Intellectual disability syndromic and non-syndromic v0.786 CEP89 Zornitza Stark Mode of inheritance for gene: CEP89 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.785 CEP89 Zornitza Stark Classified gene: CEP89 as Amber List (moderate evidence)
Intellectual disability syndromic and non-syndromic v0.785 CEP89 Zornitza Stark Gene: cep89 has been classified as Amber List (Moderate Evidence).
Intellectual disability syndromic and non-syndromic v0.8 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
Intellectual disability syndromic and non-syndromic v0.0 CEP89 Zornitza Stark gene: CEP89 was added
gene: CEP89 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland
Mode of inheritance for gene: CEP89 was set to Unknown