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Rhabdomyolysis and Metabolic Myopathy v0.164 SUCLA2 Bryony Thompson Publications for gene: SUCLA2 were set to
Rhabdomyolysis and Metabolic Myopathy v0.163 SUCLA2 Bryony Thompson Deleted their review
Rhabdomyolysis and Metabolic Myopathy v0.163 SUCLA2 Bryony Thompson commented on gene: SUCLA2
Rhabdomyolysis and Metabolic Myopathy v0.163 SUCLA2 Bryony Thompson Deleted their review
Rhabdomyolysis and Metabolic Myopathy v0.163 SUCLA2 Bryony Thompson Classified gene: SUCLA2 as Green List (high evidence)
Rhabdomyolysis and Metabolic Myopathy v0.163 SUCLA2 Bryony Thompson Gene: sucla2 has been classified as Green List (High Evidence).
Rhabdomyolysis and Metabolic Myopathy v0.162 SUCLA2 Bryony Thompson Deleted their comment
Rhabdomyolysis and Metabolic Myopathy v0.67 SUCLA2 Zornitza Stark Marked gene: SUCLA2 as ready
Rhabdomyolysis and Metabolic Myopathy v0.67 SUCLA2 Zornitza Stark Gene: sucla2 has been classified as Red List (Low Evidence).
Rhabdomyolysis and Metabolic Myopathy v0.6 SUCLA2 Bryony Thompson Classified gene: SUCLA2 as Red List (low evidence)
Rhabdomyolysis and Metabolic Myopathy v0.6 SUCLA2 Bryony Thompson Gene: sucla2 has been classified as Red List (Low Evidence).
Rhabdomyolysis and Metabolic Myopathy v0.5 SUCLA2 Bryony Thompson reviewed gene: SUCLA2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) MIM#612073; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rhabdomyolysis and Metabolic Myopathy v0.0 SUCLA2 Bryony Thompson gene: SUCLA2 was added
gene: SUCLA2 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: SUCLA2 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SUCLA2 were set to Mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) 612073