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Aminoacidopathy v1.5 MCCC1 Bryony Thompson Publications for gene: MCCC1 were set to 29152456; 31730530; 27604308; 11170888
Aminoacidopathy v1.4 MCCC1 Bryony Thompson reviewed gene: MCCC1: Rating: GREEN; Mode of pathogenicity: None; Publications: 36822454, 31730530; Phenotypes: 3-Methylcrotonyl-CoA carboxylase 1 deficiency MIM#210200, Organic acidurias; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Aminoacidopathy v1.4 MCCC1 Bryony Thompson Deleted their review
Aminoacidopathy v0.32 MCCC1 Bryony Thompson Marked gene: MCCC1 as ready
Aminoacidopathy v0.32 MCCC1 Bryony Thompson Gene: mccc1 has been classified as Green List (High Evidence).
Aminoacidopathy v0.32 MCCC1 Bryony Thompson Publications for gene: MCCC1 were set to 29152456
Aminoacidopathy v0.31 MCCC1 Bryony Thompson Classified gene: MCCC1 as Green List (high evidence)
Aminoacidopathy v0.31 MCCC1 Bryony Thompson Gene: mccc1 has been classified as Green List (High Evidence).
Aminoacidopathy v0.0 MCCC1 Bryony Thompson gene: MCCC1 was added
gene: MCCC1 was added to Disorders of branched chain amino acid metabolism. Sources: Literature
Mode of inheritance for gene: MCCC1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: MCCC1 were set to 29152456
Phenotypes for gene: MCCC1 were set to 3-methylcrotonyl-CoA carboxylase deficiency MONDO:0018950