1. Genes and Genomic Entities
  2. TCF7L2

TCF7L2

transcription factor 7 like 2
OMIM: 602228, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green TCF7L2 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • TCF7L2-related developmental disorder (monoallelic)
    Green TCF7L2 in Intellectual disability


    Level 2: Developmental disorders
    Version 10.16
    Latest signed off version: v10.0 (6 May 2026)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Developmental disorders
    • Global developmental delay
    • Intellectual disability
    • Autism
    • Attention deficit hyperactivity disorder
    • Myopia
    • Abnormality of skeletal system