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Mitochondrial disorders v6.4 ATP5E Achchuthan Shanmugasundram Tag Q4_23_promote_green was removed from gene: ATP5E.
Mitochondrial disorders v6.3 ATP5E Sarah Leigh edited their review of gene: ATP5E: Added comment: The rating of this gene has been updated to green and the mode of inheritance updated to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v6.2 ATP5E Achchuthan Shanmugasundram Source NHS GMS was added to ATP5E.
Source Expert Review Green was added to ATP5E.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v4.130 ATP5E Sarah Leigh Tag Q4_23_promote_green tag was added to gene: ATP5E.
Mitochondrial disorders v4.130 ATP5E Sarah Leigh Publications for gene: ATP5E were set to 20566710
Mitochondrial disorders v4.129 ATP5E Sarah Leigh Phenotypes for gene: ATP5E were changed from ?Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 614053 to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3, OMIM:614053; mitochondrial complex V (ATP synthase) deficiency nuclear type 3, MONDO:0013547
Mitochondrial disorders v4.128 ATP5E Sarah Leigh Classified gene: ATP5E as Amber List (moderate evidence)
Mitochondrial disorders v4.128 ATP5E Sarah Leigh Gene: atp5e has been classified as Amber List (Moderate Evidence).
Mitochondrial disorders v4.127 ATP5E Sarah Leigh edited their review of gene: ATP5E: Added comment: PMID: 34954817 reports two further cases of OMIM: 614053 who are both homozygous for ATP5E (new gene name: ATP5F1E) variant c.35A>G, p.Tyr12Cys (rs387906929), previously reported in PubMed: 20566710. Personal communication with the lead author of PMID: 34954817, confirmed that none of these cases were related to one another and so represent independent occurrences of this variant.; Changed rating: GREEN; Changed publications to: 27604308, 34954817, 20566710
Mitochondrial disorders v1.231 ATP5E Sarah Leigh Mode of inheritance for gene: ATP5E was changed from to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v1.230 ATP5E Sarah Leigh Publications for gene: ATP5E were set to PMID: 20566710
Mitochondrial disorders v1.229 ATP5E Sarah Leigh Phenotypes for gene: ATP5E were changed from ?Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 to ?Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3 614053
Mitochondrial disorders v1.228 ATP5E Sarah Leigh Classified gene: ATP5E as Red List (low evidence)
Mitochondrial disorders v1.228 ATP5E Sarah Leigh Added comment: Comment on list classification: No additional variants have been reported to date.
Mitochondrial disorders v1.228 ATP5E Sarah Leigh Gene: atp5e has been classified as Red List (Low Evidence).
Mitochondrial disorders ATP5E Louise Daugherty commented on ATP5E