PanelApp
  1. Genes and Genomic Entities
  2. ZFHX3

ZFHX3

zinc finger homeobox 3
OMIM: 104155, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green ZFHX3 in Mendeliome


Version 2.361

3 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Neurodevelopmental disorder, MONDO:0700092, ZFHX3-related
  • {Epilepsy, idiopathic generalized, susceptibility to}, MIM#621500

Green ZFHX3 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 2.30

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • {Epilepsy, idiopathic generalized, susceptibility to}, MIM#621500

    Green ZFHX3 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.61

    		2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Research
    Phenotypes
    • Neurodevelopmental disorder, MONDO:0700092, ZFHX3-related

    Green ZFHX3_SCA4_GGC STR in Mendeliome


    Version 2.361

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • spinocerebellar ataxia type 4 MONDO:0010847

    Green ZFHX3_SCA4_GGC STR in Ataxia


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.7

    Component of the following Super Panels:

  • Movement Disorders Superpanel
  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Literature
    • Expert Review Green
    • Expert Review Green
    • Literature
    Phenotypes
    • spinocerebellar ataxia type 4 MONDO:0010847

    Green ZFHX3_SCA4_GGC STR in Hereditary Neuropathy


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.23

    Component of the following Super Panels:

  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • spinocerebellar ataxia type 4 MONDO:0010847

    Green ZFHX3_SCA4_GGC STR in Repeat Disorders


    Version 1.3

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • spinocerebellar ataxia type 4 MONDO:0010847