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Mitochondrial disease v0.827 GFM2 Zornitza Stark Marked gene: GFM2 as ready
Mitochondrial disease v0.827 GFM2 Zornitza Stark Gene: gfm2 has been classified as Green List (High Evidence).
Mitochondrial disease v0.827 GFM2 Zornitza Stark Phenotypes for gene: GFM2 were changed from to Combined oxidative phosphorylation deficiency 39, OMIM #618397
Mitochondrial disease v0.826 GFM2 Zornitza Stark Publications for gene: GFM2 were set to 22700954; 26016410; 29075935
Mitochondrial disease v0.825 GFM2 Zornitza Stark Publications for gene: GFM2 were set to
Mitochondrial disease v0.824 GFM2 Zornitza Stark Mode of inheritance for gene: GFM2 was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.823 GFM2 Zornitza Stark Mode of inheritance for gene: GFM2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.821 GFM2 Chirag Patel reviewed gene: GFM2: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 22700954, 26016410, 29075935; Phenotypes: Combined oxidative phosphorylation deficiency 39, OMIM #618397; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.0 GFM2 Zornitza Stark gene: GFM2 was added
gene: GFM2 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: GFM2 was set to Unknown