1. Genes and Genomic Entities
  2. CCNK

CCNK

cyclin K
OMIM: 603544, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red CCNK in DDG2P


Version 3.90
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
    • Syndromic Neurodevelopmental Disorder with Distinctive Facial Dysmorphism