1. Genes and Genomic Entities
  2. TCF7L2

TCF7L2

transcription factor 7 like 2
OMIM: 602228, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red TCF7L2 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Green TCF7L2 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
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • TCF7L2-related developmental disorder (monoallelic)
    Green TCF7L2 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 6.13
    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, 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