PanelApp
  1. Genes and Genomic Entities
  2. CCT3

CCT3

chaperonin containing TCP1 subunit 3
OMIM: 600114, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green CCT3 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with speech or visual impairment and brain hypomyelination, MIM# 621034

Green CCT3 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.119

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with speech or visual impairment and brain hypomyelination, MIM# 621034

    Green CCT3 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.83

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • neurodevelopmental disorder MONDO:0700092, CCT3-related