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Early onset or syndromic epilepsy v3.14 COX15 Arina Puzriakova Phenotypes for gene: COX15 were changed from Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 615119; Leigh syndrome 256000 to Mitochondrial complex IV deficiency, nuclear type 6, OMIM:615119
Early onset or syndromic epilepsy v1.191 COX15 Rebecca Foulger Source Wessex and West Midlands GLH was added to COX15.
Early onset or syndromic epilepsy v1.190 COX15 Rebecca Foulger Source NHS GMS was added to COX15.
Early onset or syndromic epilepsy v1.189 COX15 Rebecca Foulger reviewed gene: COX15: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Early onset or syndromic epilepsy v1.188 COX15 Tracy Lester reviewed gene: COX15: Rating: AMBER; Mode of pathogenicity: ; Publications: 12474143; Phenotypes: Cardioencephalomyopathy fatal infantile due to cytochrome c oxidase deficiency 2 615119 , Leigh syndrome due to cytochrome c oxidase deficiency, 256000; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v0.1589 COX15 Sarah Leigh Marked gene: COX15 as ready
Early onset or syndromic epilepsy v0.1589 COX15 Sarah Leigh Added comment: Comment when marking as ready: Based on reviewers' comments.
Early onset or syndromic epilepsy v0.1589 COX15 Sarah Leigh Gene: cox15 has been classified as Amber List (Moderate Evidence).
Early onset or syndromic epilepsy v0.1443 COX15 Sarah Leigh Mode of inheritance for gene: COX15 was changed from to BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v0.1442 COX15 Sarah Leigh Phenotypes for gene: COX15 were changed from to Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2 615119; Leigh syndrome 256000
Early onset or syndromic epilepsy v0.1441 COX15 Sarah Leigh Publications for gene: COX15 were set to
Early onset or syndromic epilepsy COX15 Zornitza Stark reviewed gene: COX15
Early onset or syndromic epilepsy COX15 Sarah Leigh Added gene to panel