KDM4B

lysine demethylase 4B
OMIM: 609765, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red KDM4B in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Green KDM4B 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
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • KDM4B-related Developmental Disorder
    Green KDM4B in Intellectual disability - microarray and sequencing

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 5.544
    Latest signed off version: v5.0 (22 Mar 2023)

    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