CNOT3

CCR4-NOT transcription complex subunit 3
OMIM: 604910, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green CNOT3 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 0.205

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672

Green CNOT3 in Mendeliome


Version 1.2374

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672

Green CNOT3 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
  • Genetic Health Queensland
Phenotypes
  • Intellectual developmental disorder with speech delay, autism, and dysmorphic facies 618672

Amber CNOT3 in Cerebral vascular malformations


Level 2: Neurology and neurodevelopmental disorders
Version 1.0

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Moya Moya
    • Intellectual developmental disorder with speech delay, autism, and dysmorphic facies, MIM# 618672

    Green CNOT3 in Fetal anomalies


    Version 1.314

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Genetic Health Queensland
    Phenotypes
    • Intellectual developmental disorder with speech delay, autism, and dysmorphic facies , MIM#618672