1. Genes and Genomic Entities
  2. CCNK

CCNK

cyclin K
OMIM: 603544, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CCNK in DDG2P


Version 8.2
Latest signed off version: v8.0 (12 Aug 2026)

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
    Amber CCNK in Intellectual disability


    Level 2: Developmental disorders
    Version 11.28
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • ?Intellectual developmental disorder with hypertelorism and distinctive facies, OMIM:618147
    • intellectual developmental disorder with hypertelorism and distinctive facies, MONDO:0029143
    Tags
    • Q4_25_promote_green