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Intellectual disability syndromic and non-syndromic v0.645 ALS2 Zornitza Stark Marked gene: ALS2 as ready
Intellectual disability syndromic and non-syndromic v0.645 ALS2 Zornitza Stark Gene: als2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.645 ALS2 Zornitza Stark Phenotypes for gene: ALS2 were changed from to Spastic paralysis, infantile onset ascending, MIM#607225
Intellectual disability syndromic and non-syndromic v0.644 ALS2 Zornitza Stark Mode of inheritance for gene: ALS2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.643 ALS2 Zornitza Stark Classified gene: ALS2 as Red List (low evidence)
Intellectual disability syndromic and non-syndromic v0.643 ALS2 Zornitza Stark Gene: als2 has been classified as Red List (Low Evidence).
Intellectual disability syndromic and non-syndromic v0.1 ALS2 Zornitza Stark reviewed gene: ALS2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Spastic paralysis, infantile onset ascending, MIM#607225; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Intellectual disability syndromic and non-syndromic v0.0 ALS2 Zornitza Stark gene: ALS2 was added
gene: ALS2 was added to Intellectual disability, syndromic and non-syndromic_GHQ. Sources: Expert Review Green,Genetic Health Queensland
Mode of inheritance for gene: ALS2 was set to Unknown