1. Genes and Genomic Entities
  2. CCT7

CCT7

chaperonin containing TCP1 subunit 7
OMIM: 605140, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CCT7 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • CCT7-related neurodevelopmental disorder with brain abnormalities
    Red CCT7 in Intellectual disability


    Level 2: Developmental disorders
    Version 10.17
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Literature
    Phenotypes
    • CCT7-related neurodevelopmental disorder with brain abnormalities