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Mitochondrial disease v0.940 PUS1 Zornitza Stark Phenotypes for gene: PUS1 were changed from Myopathy, lactic acidosis, and sideroblastic anaemia 1, MIM# 600462 to Myopathy, lactic acidosis, and sideroblastic anaemia 1, MIM# 600462
Mitochondrial disease v0.939 PUS1 Zornitza Stark Marked gene: PUS1 as ready
Mitochondrial disease v0.939 PUS1 Zornitza Stark Gene: pus1 has been classified as Green List (High Evidence).
Mitochondrial disease v0.939 PUS1 Zornitza Stark Phenotypes for gene: PUS1 were changed from to Myopathy, lactic acidosis, and sideroblastic anaemia 1, MIM# 600462
Mitochondrial disease v0.938 PUS1 Zornitza Stark Publications for gene: PUS1 were set to
Mitochondrial disease v0.937 PUS1 Zornitza Stark Mode of inheritance for gene: PUS1 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.936 PUS1 Zornitza Stark edited their review of gene: PUS1: Changed phenotypes: Myopathy, lactic acidosis, and sideroblastic anaemia 1, MIM# 600462
Mitochondrial disease v0.0 PUS1 Zornitza Stark gene: PUS1 was added
gene: PUS1 was added to Mitochondrial_AGHA_VCGS. Sources: Expert Review Green,Australian Genomics Health Alliance Mitochondrial Flagship,Victorian Clinical Genetics Services
Mode of inheritance for gene: PUS1 was set to Unknown