1. Genes and Genomic Entities
  2. DENND5B

DENND5B

DENN domain containing 5B
OMIM: 617279, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red DENND5B in DDG2P


Version 6.424
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • DENND5B-related neurodevelopmental disorder with cortical migration and white matter abnormalities
    Tags
    • de novo
    • gene-checked
    Amber DENND5B in Early onset or syndromic epilepsy


    Level 2: Neurology
    Version 8.125
    Latest signed off version: v8.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • DENND5B associated neurodevelopmental disorder
    Tags
    • gene-checked
    Green DENND5B in Intellectual disability


    Level 2: Developmental disorders
    Version 9.285
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • DENND5B associated neurodevelopmental disorder
    Tags
    • gene-checked