TNK2

tyrosine kinase non receptor 2
OMIM: 606994, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Amber TNK2 in Mendeliome Version 1.4605	2 reviews	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 1.389 Component of the following Super Panels: Progressive Neurological Conditions	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Victorian Clinical Genetics Services Australian Genomics Health Alliance Epilepsy Flagship Phenotypes severe infantile onset epilepsy
Amber TNK2 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.608	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Amber Phenotypes late onset infantile epilepsy Mayer-Rokitansky-Küster-Hauser syndrome
Amber TNK2 in Disorders of immune dysregulation Level 2: Immunological disorders Version 1.39 Component of the following Super Panels: Immunological disorders_SuperPanel	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Amber Phenotypes late onset infantile epilepsy Mayer-Rokitansky-Küster-Hauser syndrome
Amber TNK2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.709	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Victorian Clinical Genetics Services Expert Review Amber Phenotypes late onset infantile epilepsy Mayer-Rokitansky-Küster-Hauser syndrome