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Mitochondrial disease v0.1375 ATPAF2 Zornitza Stark Marked gene: ATPAF2 as ready
Mitochondrial disease v0.1375 ATPAF2 Zornitza Stark Gene: atpaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.1375 ATPAF2 Zornitza Stark Phenotypes for gene: ATPAF2 were changed from to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1, OMIM# 604273
Mitochondrial disease v0.1374 ATPAF2 Zornitza Stark Publications for gene: ATPAF2 were set to
Mitochondrial disease v0.1373 ATPAF2 Zornitza Stark Mode of inheritance for gene: ATPAF2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Classified gene: ATPAF2 as Red List (low evidence)
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Gene: atpaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.823 ATPAF2 Chirag Patel Classified gene: ATPAF2 as Red List (low evidence)
Mitochondrial disease v0.823 ATPAF2 Chirag Patel Gene: atpaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Classified gene: ATPAF2 as Red List (low evidence)
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Gene: atpaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Classified gene: ATPAF2 as Red List (low evidence)
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Gene: atpaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Classified gene: ATPAF2 as Red List (low evidence)
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Gene: atpaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Classified gene: ATPAF2 as Red List (low evidence)
Mitochondrial disease v0.822 ATPAF2 Chirag Patel Gene: atpaf2 has been classified as Red List (Low Evidence).
Mitochondrial disease v0.821 ATPAF2 Chirag Patel reviewed gene: ATPAF2: Rating: RED; Mode of pathogenicity: None; Publications: PMID: 14757859; Phenotypes: ?Mitochondrial complex V (ATP synthase) deficiency, nuclear type 1, OMIM# 604273; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disease v0.0 ATPAF2 Zornitza Stark gene: ATPAF2 was added
gene: ATPAF2 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: ATPAF2 was set to Unknown