1. Genes and Genomic Entities
  2. FOXP4

FOXP4

forkhead box P4
OMIM: 608924, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels
Green FOXP4 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 8.4
Latest signed off version: v8.0 (12 Aug 2026)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • Congenital diaphragmatic hernia
  • Neurodevelopmental disorder
  • multiple congenital abnormalities
Tags
  • gene-checked
Green FOXP4 in DDG2P


Version 8.1
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • DD-Gene2Phenotype
    Phenotypes
    • FOXP4-related Developmental Disorder
    Tags
    • gene-checked
    • de novo
    Green FOXP4 in Paediatric disorders - additional genes


    Level 2: Developmental disorders
    Version 8.13
    Latest signed off version: v8.8 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder
    • multiple congenital abnormalities
    Tags
    • gene-checked
    Amber FOXP4 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.23
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Neurodevelopmental disorder
    • multiple congenital abnormalities
    Tags
    • gene-checked
    Amber FOXP4 in Monogenic short stature


    Level 2: Endocrinology
    Version 2.9
    Latest signed off version: v2.8 (12 Aug 2026)

    		review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    • Expert Review Amber
    Phenotypes
    • Neurodevelopmental disorder
    • multiple congenital abnormalities
    Tags
    • gene-checked