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Mitochondrial disease v0.862 ATP5E Bryony Thompson Publications for gene: ATP5E were set to 20566710; 27626380; 20026007
Mitochondrial disease v0.861 ATP5E Bryony Thompson Classified gene: ATP5E as Green List (high evidence)
Mitochondrial disease v0.861 ATP5E Bryony Thompson Gene: atp5e has been classified as Green List (High Evidence).
Mitochondrial disease v0.688 ATP5E Ain Roesley reviewed gene: ATP5E: Rating: GREEN; Mode of pathogenicity: None; Publications: 34954817; Phenotypes: Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 MIM#614053; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Mitochondrial disease v0.445 ATP5E Zornitza Stark Marked gene: ATP5E as ready
Mitochondrial disease v0.445 ATP5E Zornitza Stark Added comment: Comment when marking as ready: HGNC approved name ATP5F1E.
Mitochondrial disease v0.445 ATP5E Zornitza Stark Gene: atp5e has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.445 ATP5E Zornitza Stark Tag new gene name tag was added to gene: ATP5E.
Mitochondrial disease v0.203 ATP5E Zornitza Stark Marked gene: ATP5E as ready
Mitochondrial disease v0.203 ATP5E Zornitza Stark Gene: atp5e has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.203 ATP5E Zornitza Stark Phenotypes for gene: ATP5E were changed from to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 MIM#614053
Mitochondrial disease v0.202 ATP5E Zornitza Stark Publications for gene: ATP5E were set to
Mitochondrial disease v0.201 ATP5E Zornitza Stark Mode of inheritance for gene: ATP5E was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.91 ATP5E Bryony Thompson Classified gene: ATP5E as Amber List (moderate evidence)
Mitochondrial disease v0.91 ATP5E Bryony Thompson Gene: atp5e has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.90 ATP5E Bryony Thompson reviewed gene: ATP5E: Rating: AMBER; Mode of pathogenicity: None; Publications: 20566710, 27626380, 20026007; Phenotypes: Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 MIM#614053; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.0 ATP5E Zornitza Stark gene: ATP5E was added
gene: ATP5E 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: ATP5E was set to Unknown