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C175328Level 6

Inactivating KMT2C Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the KMT2C gene that inhibits expression or results in the translation of either low-activity or inactive forms of the histone-lysine N- methyltransferase 2C protein.

**Synonyms:** - Inactivating HALR Gene Mutation - Inactivating KMT2C Mutation - Inactivating Lysine (K)-Specific Methyltransferase 2C Gene Mutation - Inactivating Lysine Methyltransferase 2C Gene Mutation - Inactivating MLL3 Gene Mutation - Inactivating Myeloid/Lymphoid or Mixed-Lineage Leukemia 3 Gene Mutation - KMT2C Gene Inactivation - KMT2C Inactivating Gene Mutation - KMT2C Inactivating Mutation - KMT2C Inactivation - KMT2C Loss of Function Gene Mutation - KMT2C Loss of Function Mutation - Loss of Function KMT2C Gene Mutation - Loss of Function KMT2C Mutation

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