CDK20

cyclin dependent kinase 20
OMIM: 610076, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels
Amber CDK20 in Hydrocephalus


Level 2: Neurology
Version 5.14
Latest signed off version: v5.0 (7 Aug 2024)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Amber
Phenotypes
  • ciliopathy, MONDO:0005308
  • Ventriculomegaly, HP:0002119
  • hydrocephalus, MONDO:0001150
Tags
  • Q3_26_promote_green
Red CDK20 in Holoprosencephaly


Level 2: Neurology
Version 6.3
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Cerebral malformation
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    Phenotypes
    • ciliopathy, MONDO:0005308
    • Ventriculomegaly, HP:0002119
    • hydrocephalus, MONDO:0001150
    • holoprosencephaly, MONDO:0016296
    Amber CDK20 in Fetal anomalies


    Level 2: Fetal (including NIPD)
    Version 7.33
    Latest signed off version: v7.0 (6 May 2026)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • ciliopathy, MONDO:0005308
    • Ventriculomegaly, HP:0002119
    • hydrocephalus, MONDO:0001150
    Tags
    • Q3_26_promote_green
    Amber CDK20 in Clefting


    Level 2: Musculoskeletal
    Version 7.8
    Latest signed off version: v7.0 (6 May 2026)

    Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Amber
    Phenotypes
    • ciliopathy, MONDO:0005308
    • Ventriculomegaly, HP:0002119
    • hydrocephalus, MONDO:0001150
    Tags
    • Q3_26_promote_green
    Amber CDK20 in Intellectual disability


    Level 2: Developmental disorders
    Version 10.85
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    • Expert Review Amber
    Phenotypes
    • ciliopathy, MONDO:0005308
    • Ventriculomegaly, HP:0002119
    • hydrocephalus, MONDO:0001150
    Red CDK20 in Proteinuric renal disease


    Level 2: Renal
    Version 6.13
    Latest signed off version: v6.0 (6 May 2026)

    Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease
  • review Not set
    Sources
    • NHS GMS
    Phenotypes
    • Chronic kidney disease