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Early onset or syndromic epilepsy v8.117 CCT8 Ida Ertmanska Classified gene: CCT8 as Amber List (moderate evidence)
Early onset or syndromic epilepsy v8.117 CCT8 Ida Ertmanska Gene: cct8 has been classified as Amber List (Moderate Evidence).
Early onset or syndromic epilepsy v8.116 CCT8 Ida Ertmanska gene: CCT8 was added
gene: CCT8 was added to Early onset or syndromic epilepsy. Sources: Literature
Mode of inheritance for gene: CCT8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: CCT8 were set to 39480921
Phenotypes for gene: CCT8 were set to CCT8-related neurodevelopmental disorder with brain abnormalities
Review for gene: CCT8 was set to AMBER
Added comment: PMID: 39480921 Kraft et al., 2024
Report of 2 individuals (20yo male and 79yo male) with heterozygous CCT7 variants: c.925_929del p.(Asn309Hisfs*16) - de novo & c.1166_1169delAAAG, p.(Glu389Glyfs*3) - inheritance not known. Patients presented with DD/ID (2/2), cerebral/pyramidal signs (1), seizures (2/2) and MRI abnormalities: Polymicrogyria (2/2).

CCT8 is not yet associated with a disease entity in OMIM (accessed 20th Feb 2026).
Sources: Literature