1. Genes and Genomic Entities
  2. TM4SF20

TM4SF20

transmembrane 4 L six family member 20
OMIM: 615404, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red TM4SF20 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 Red
    Phenotypes
    • SPECIFIC LANGUAGE IMPAIRMENT 5 615432
    Red TM4SF20 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, imprinted status unknown
    Sources
    • Expert Review Red
    Phenotypes
    • early language delay
    • {Specific language impairment 5}, 615432