PanelApp
  1. Genes and Genomic Entities
  2. TCF4

TCF4

transcription factor 4
OMIM: 602272, Gene2Phenotype

13 panels

Panel Reviews Mode of inheritance Details
13 panels

Green TCF4 in Angelman Rett like syndromes


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.13

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Pitt-Hopkins syndrome, MIM# 610954

Green TCF4 in Autism


Level 2: Neurology and neurodevelopmental disorders
Version 0.224

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Green TCF4 in Cerebral Palsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.400

3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Pitt-Hopkins syndrome, MIM# 610954

No list TCF4 in Corneal Dystrophy


Level 2: Ophthalmological disorders
Version 1.13

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Removed
  • Victorian Clinical Genetics Services
Phenotypes
  • Corneal dystrophy, Fuchs endothelial, 3, MIM# 613267
Tags
  • STR

Green TCF4 in Mendeliome


Version 1.3512

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Pitt-Hopkins syndrome, MIM# 610954

Green TCF4 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.357

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Pitt-Hopkins syndrome, MIM# 610954

Green TCF4 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.267

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Pitt-Hopkins syndrome, MIM# 610954

    Green TCF4 in Callosome


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.565

    		0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green TCF4 in Regression


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.594

    		0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green TCF4 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.410

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genetic Health Queensland
    Phenotypes
    • Pitt-Hopkins syndrome MONDO:0012589

    Green TCF4 in Fetal anomalies


    Version 1.465

    		1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    • Victorian Clinical Genetics Services
    Phenotypes
    • Pitt-Hopkins syndrome, MIM# 610954

    Green TCF4_FECD3_CTG STR in Corneal Dystrophy


    Level 2: Ophthalmological disorders
    Version 1.13

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Corneal dystrophy, Fuchs endothelial, 3 MIM#613267

    Green TCF4_FECD3_CTG STR in Repeat Disorders


    Version 0.269

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Corneal dystrophy, Fuchs endothelial, 3 MIM#613267
    Tags
    • adult-onset