NCOR1

nuclear receptor corepressor 1
OMIM: 600849, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red NCOR1 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Red NCOR1 in DDG2P


Version 3.88
Latest signed off version: v3.1 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • NCOR1-related developmental disorder