World Of Taxonomy
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

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