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Rhabdomyolysis and Metabolic Myopathy v2.0 TSEN54 Gene migrated from ENSG00000182173 to ENSG00000182173 (gene set migration)
Rhabdomyolysis and Metabolic Myopathy v0.67 TSEN54 Zornitza Stark Marked gene: TSEN54 as ready
Rhabdomyolysis and Metabolic Myopathy v0.67 TSEN54 Zornitza Stark Gene: tsen54 has been classified as Red List (Low Evidence).
Rhabdomyolysis and Metabolic Myopathy v0.67 TSEN54 Zornitza Stark Publications for gene: TSEN54 were set to
Rhabdomyolysis and Metabolic Myopathy v0.50 TSEN54 Bryony Thompson edited their review of gene: TSEN54: Changed publications: 23177318; Changed phenotypes: Pontocerebellar hypoplasia type 2A MIM#277470
Rhabdomyolysis and Metabolic Myopathy v0.50 TSEN54 Bryony Thompson changed review comment from: Cannot find any evidence that rhabdomyolysis is a feature of the condition. Hypertonia reported which is neurogenic.; to: Single case reported with recurrent rhabdomyolysis and PCH with a homozygous variant.
Rhabdomyolysis and Metabolic Myopathy v0.7 TSEN54 Bryony Thompson Classified gene: TSEN54 as Red List (low evidence)
Rhabdomyolysis and Metabolic Myopathy v0.7 TSEN54 Bryony Thompson Gene: tsen54 has been classified as Red List (Low Evidence).
Rhabdomyolysis and Metabolic Myopathy v0.6 TSEN54 Bryony Thompson reviewed gene: TSEN54: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Pontocerebellar hypoplasia; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Rhabdomyolysis and Metabolic Myopathy v0.0 TSEN54 Bryony Thompson gene: TSEN54 was added
gene: TSEN54 was added to Rhabdomyolysis_RMH. Sources: Royal Melbourne Hospital,Expert Review Green
Mode of inheritance for gene: TSEN54 was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: TSEN54 were set to ?Pontocerebellar hypoplasia type 5 610204; Pontocerebellar hypoplasia type 4 225753; Pontocerebellar hypoplasia type 2A 277470