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NTRK2

neurotrophic receptor tyrosine kinase 2
3 disorders 2 untyped 1 causative 9q21.33 gene with protein product
HGNC:8032MonarchNCBI Gene 4915ENSG00000148053UniProt Q16620OMIM 600456

Aliases: TRKB.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Genetic Developmental and Epileptic Encephalopathy causative
mechanism: Genetic Lesion Beyond the Channelopathies
subtype: DEE58
scoped to subtype: DEE58
Huntington Disease untyped
Pathophysiological Role
NTRK Fusion-Positive Cancer untyped
Somatic Gene Fusions

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.