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Early onset or syndromic epilepsy v3.13 COX10 Arina Puzriakova Phenotypes for gene: COX10 were changed from to Mitochondrial complex IV deficiency, nuclear type 3, OMIM:619046
Early onset or syndromic epilepsy v3.12 COX10 Arina Puzriakova Mode of inheritance for gene: COX10 was changed from to BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v1.191 COX10 Rebecca Foulger Source Wessex and West Midlands GLH was added to COX10.
Early onset or syndromic epilepsy v1.190 COX10 Rebecca Foulger Source NHS GMS was added to COX10.
Early onset or syndromic epilepsy v1.189 COX10 Rebecca Foulger reviewed gene: COX10: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Early onset or syndromic epilepsy v1.188 COX10 Tracy Lester reviewed gene: COX10: Rating: AMBER; Mode of pathogenicity: ; Publications: 10767350; Phenotypes: Leigh syndrome due to mitochondrial COX4 deficiency, 256000 , Mitochondrial, Mitochondrial complex IV deficiency, 220110; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Early onset or syndromic epilepsy v0.1589 COX10 Sarah Leigh Marked gene: COX10 as ready
Early onset or syndromic epilepsy v0.1589 COX10 Sarah Leigh Added comment: Comment when marking as ready: Based on reviewers' comments.
Early onset or syndromic epilepsy v0.1589 COX10 Sarah Leigh Gene: cox10 has been classified as Amber List (Moderate Evidence).
Early onset or syndromic epilepsy COX10 Zornitza Stark reviewed gene: COX10
Early onset or syndromic epilepsy COX10 Sarah Leigh Added gene to panel