C136639Level 7
Non-synonymous MAP2K Family Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A point mutation in a gene that is a member of the MAP2K gene family that encodes an amino acid substitution in a MAP2K family protein.
**Synonyms:** - MAP2K Family Gene Missense Mutation - MEK Family Gene Missense Mutation - Non-synonymous MAPKK Family Gene Mutation - Non-synonymous MEK Family Gene Mutation - Non-synonymous Mitogen-Activated Protein Kinase Kinase Family Gene Mutation
GET
/api/v1/systems/nci_thesaurus/nodes/C136639Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.