1. Genes and Genomic Entities
  2. TNK2

TNK2

tyrosine kinase non receptor 2
OMIM: 606994, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber TNK2 in Early onset or syndromic epilepsy

Level 3: Inherited Epilepsy Syndromes
Level 2: Neurology and neurodevelopmental disorders
Version 4.193
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Wessex and West Midlands GLH
    • NHS GMS
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    Phenotypes
    • severe autosomal recessive infantile onset epilepsy
    • EE
    Tags
    • watchlist