1. Genes and Genomic Entities
  2. ZFHX3

ZFHX3

zinc finger homeobox 3
OMIM: 104155, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red ZFHX3 in COVID-19 research


Level 2: Viral research
Version 1.142

review Not set
Sources
  • Literature
Amber ZFHX3 in Ataxia and cerebellar anomalies - narrow panel


Version 5.3
Latest signed off version: v5.0 (1 May 2024)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies - childhood onset

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    • Expert Review Amber
    Phenotypes
    • Spinocerebellar ataxia 4, OMIM:600223
    • spinocerebellar ataxia type 4, MONDO:0010847
    Tags
    • STR
    Red ZFHX3 in DDG2P


    Version 4.3
    Latest signed off version: v4.0 (1 May 2024)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • ZFHX3-related developmental disorder (monoallelic)
    Amber ZFHX3 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 6.11
    Latest signed off version: v6.0 (1 May 2024)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • syndromic intellectual disability
    Tags
    • Q1_24_promote_green
    • Q1_24_NHS_review