1. Genes and Genomic Entities
  2. TCF20

TCF20

transcription factor 20
OMIM: 603107, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber TCF20 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • PAGE DD-Gene2Phenotype
Phenotypes
  • Developmental delay with variable intellectual impairment and behavioral abnormalities 618430
  • TCF20 syndrome
  • Developmental delay with variable intellectual impairment and behavioral abnormalities
Green TCF20 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 Green
    Phenotypes
    • TCF20 syndrome
    Green TCF20 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, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • BRIDGE study SPEED NEURO Tier1 Gene
    Phenotypes
    • TCF20 syndrome
    • Intellectual disability
    • developmental delay
    • Developmental delay with variable intellectual impairment and behavioral abnormalities 618430
    Tags
    • de novo