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Dystonia - isolated/combined v0.48 KMT2B Zornitza Stark reviewed gene: KMT2B: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Dystonia 28, childhood-onset 617284, MONDO:0015004; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Dystonia - isolated/combined v0.48 KMT2B Zornitza Stark Marked gene: KMT2B as ready
Dystonia - isolated/combined v0.48 KMT2B Zornitza Stark Gene: kmt2b has been classified as Green List (High Evidence).
Dystonia - isolated/combined v0.48 KMT2B Zornitza Stark Phenotypes for gene: KMT2B were changed from early-onset dystonia; Dystonia 28, childhood-onset 617284 to early-onset dystonia; Dystonia 28, childhood-onset 617284; MONDO:0015004
Dystonia - isolated/combined v0.47 KMT2B Zornitza Stark Publications for gene: KMT2B were set to
Dystonia - isolated/combined v0.46 KMT2B Zornitza Stark Mode of inheritance for gene: KMT2B was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Dystonia - isolated/combined v0.0 KMT2B Bryony Thompson gene: KMT2B was added
gene: KMT2B was added to Dystonia - isolated/combined_RMH. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: KMT2B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: KMT2B were set to early-onset dystonia; Dystonia 28, childhood-onset 617284