Inactivating FBXW7 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the FBXW7 gene that either inhibits expression or results in the translation of an inactive F-box/WD repeat-containing protein 7.

**Synonyms:** - FBXW7 Gene Inactivation - FBXW7 Inactivating Gene Mutation - FBXW7 Inactivating Mutation - FBXW7 Loss of Function Gene Mutation - FBXW7 Loss of Function Mutation - FBXW7 Loss of Function Mutation - Inactivating AGO Gene Mutation - Inactivating Archipelago Homolog Gene Mutation - Inactivating CDC4 Gene Mutation - Inactivating F-Box and WD Repeat Domain Containing 7 Gene Mutation - Inactivating FBW6 Gene Mutation - Inactivating FBW7 Gene Mutation - Inactivating FBX30 Gene Mutation - Inactivating FBXW6 Gene Mutation - Inactivating FBXW7 Mutation - Inactivating SEL-10 Gene Mutation - Inactivating SEL10 Gene Mutation