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Mitochondrial disease v0.806 MTFMT Zornitza Stark Marked gene: MTFMT as ready
Mitochondrial disease v0.806 MTFMT Zornitza Stark Gene: mtfmt has been classified as Green List (High Evidence).
Mitochondrial disease v0.806 MTFMT Zornitza Stark Phenotypes for gene: MTFMT were changed from to Combined oxidative phosphorylation deficiency 15, MIM# 614947; Mitochondrial complex I deficiency, nuclear type 27, MIM# 618248
Mitochondrial disease v0.805 MTFMT Zornitza Stark Publications for gene: MTFMT were set to
Mitochondrial disease v0.804 MTFMT Zornitza Stark Mode of inheritance for gene: MTFMT was changed from BIALLELIC, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.803 MTFMT Zornitza Stark Mode of inheritance for gene: MTFMT was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.802 MTFMT Zornitza Stark reviewed gene: MTFMT: Rating: GREEN; Mode of pathogenicity: None; Publications: 21907147, 23499752, 24461907, 22499348; Phenotypes: Combined oxidative phosphorylation deficiency 15, MIM# 614947, Mitochondrial complex I deficiency, nuclear type 27, MIM# 618248; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.0 MTFMT Zornitza Stark gene: MTFMT was added
gene: MTFMT 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: MTFMT was set to Unknown