C36701Level 7
Inactivating MSH6 Gene Mutation
**Semantic type:** Cell or Molecular Dysfunction
**Definition:** A change in the nucleotide sequence of the MSH6 gene that either inhibits expression or results in the translation of an inactive DNA mismatch repair protein Msh6 protein.
**Synonyms:** - Inactivating MSH6 Mutation - Loss of Function HNPCC5 Gene Mutation - Loss of Function MSH6 Gene Mutation - Loss of Function MSH6 Mutation - Loss of Function MutS Homolog 6 Gene Mutation - Loss of Function MutS, E. coli, Homolog of, 6 Gene Mutation - MSH6 Gene Inactivation - MSH6 Loss of Function Gene Mutation - MSH6 Loss of Function Mutation - hMSH6 Mismatch Repair Gene Inactivation
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