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