PanelApp
  1. Genes and Genomic Entities
  2. TNK2

TNK2

tyrosine kinase non receptor 2
OMIM: 606994, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber TNK2 in Mendeliome


Version 1.3512

1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • late onset infantile epilepsy
  • Mayer-Rokitansky-Küster-Hauser syndrome

Amber TNK2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.267

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • severe infantile onset epilepsy