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Mitochondrial disease v2.0 GATB Gene migrated from ENSG00000059691 to ENSG00000059691 (gene set migration)
Mitochondrial disease v0.983 GATB Bryony Thompson Phenotypes for gene: GATB were changed from Mitochondrial cardiomyopathy to inborn mitochondrial metabolism disorder MONDO:0004069
Mitochondrial disease v0.982 GATB Bryony Thompson Publications for gene: GATB were set to 30283131; 38703036
Mitochondrial disease v0.981 GATB Bryony Thompson Publications for gene: GATB were set to 30283131
Mitochondrial disease v0.981 GATB Bryony Thompson Classified gene: GATB as Amber List (moderate evidence)
Mitochondrial disease v0.981 GATB Bryony Thompson Gene: gatb has been classified as Amber List (Moderate Evidence).
Mitochondrial disease v0.980 GATB Bryony Thompson reviewed gene: GATB: Rating: AMBER; Mode of pathogenicity: None; Publications: 30283131, 38703036; Phenotypes: inborn mitochondrial metabolism disorder MONDO:0004069; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.235 GATB Zornitza Stark Marked gene: GATB as ready
Mitochondrial disease v0.235 GATB Zornitza Stark Gene: gatb has been classified as Red List (Low Evidence).
Mitochondrial disease v0.235 GATB Zornitza Stark gene: GATB was added
gene: GATB was added to Mitochondrial disease. Sources: NHS GMS
Mode of inheritance for gene: GATB was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: GATB were set to 30283131
Phenotypes for gene: GATB were set to Mitochondrial cardiomyopathy
Review for gene: GATB was set to RED
Added comment: Single family reported with two affected siblings.
Sources: NHS GMS