1. Genes and Genomic Entities
  2. KDM4B

KDM4B

lysine demethylase 4B
OMIM: 609765, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green KDM4B in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.1
Latest signed off version: v7.0 (6 May 2026)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
Phenotypes
  • Intellectual developmental disorder, autosomal dominant 65, OMIM:619320
Green KDM4B in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • KDM4B-related Developmental Disorder
    Green KDM4B in Intellectual disability


    Level 2: Developmental disorders
    Version 10.2
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Global developmental delay, intellectual disability and neuroanatomical defects