CNOT2

CCR4-NOT transcription complex subunit 2
OMIM: 604909, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Green CNOT2 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.66
Signed off v.3.2 on 13 Feb 2020

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Radboud University Medical Center, Nijmegen
    • Literature
    Phenotypes
    • Intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies, 618608