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Callosome v0.354 COX15 Zornitza Stark Marked gene: COX15 as ready
Callosome v0.354 COX15 Zornitza Stark Gene: cox15 has been classified as Red List (Low Evidence).
Callosome v0.354 COX15 Zornitza Stark Phenotypes for gene: COX15 were changed from to Mitochondrial complex IV deficiency, nuclear type 6, MIM# 615119
Callosome v0.353 COX15 Zornitza Stark Publications for gene: COX15 were set to
Callosome v0.352 COX15 Zornitza Stark Mode of inheritance for gene: COX15 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Callosome v0.351 COX15 Zornitza Stark Classified gene: COX15 as Red List (low evidence)
Callosome v0.351 COX15 Zornitza Stark Gene: cox15 has been classified as Red List (Low Evidence).
Callosome v0.350 COX15 Zornitza Stark reviewed gene: COX15: Rating: RED; Mode of pathogenicity: None; Publications: 33746038, 32232962, 26959537, 21412973, 12474143, 15235026; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 6, MIM# 615119; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Callosome v0.0 COX15 Zornitza Stark gene: COX15 was added
gene: COX15 was added to Corpus callosum agenesis, Callosome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: COX15 was set to Unknown