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Ataxia v1.140 Bryony Thompson Copied STR FGF14_SCA27B_GAA from panel Ataxia - adult onset
Ataxia v1.140 FGF14_SCA27B_GAA Bryony Thompson STR: FGF14_SCA27B_GAA was added
STR: FGF14_SCA27B_GAA was added to Ataxia. Sources: Expert Review Green,Literature
Mode of inheritance for STR: FGF14_SCA27B_GAA was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for STR: FGF14_SCA27B_GAA were set to 37165652; 36516086; 36493768
Phenotypes for STR: FGF14_SCA27B_GAA were set to Spinocerebellar ataxia type 27B MONDO:0012247; Spinocerebellar ataxia 50; late-onset cerebellar ataxias (LOCAs)
Ataxia v0.112 FGF14 Bryony Thompson Marked gene: FGF14 as ready
Ataxia v0.112 FGF14 Bryony Thompson Gene: fgf14 has been classified as Green List (High Evidence).
Ataxia v0.112 FGF14 Bryony Thompson Classified gene: FGF14 as Green List (high evidence)
Ataxia v0.112 FGF14 Bryony Thompson Gene: fgf14 has been classified as Green List (High Evidence).
Ataxia v0.111 FGF14 Bryony Thompson gene: FGF14 was added
gene: FGF14 was added to Ataxia - paediatric. Sources: Expert list
Mode of inheritance for gene: FGF14 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: FGF14 were set to Spinocerebellar ataxia 27 MIM#609307
Review for gene: FGF14 was set to GREEN
Added comment: Onset in late-childhood to early adulthood (12 to 20 years).
Sources: Expert list