Inactivating RAC2 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the RAC2 gene that either inhibits expression or results in the translation of an inactive Ras-related C3 botulinum toxin substrate 2 protein.

**Synonyms:** - Inactivating EN-7 Gene Mutation - Inactivating Gx Gene Mutation - Inactivating RAC2 Mutation - Inactivating Rac Family Small GTPase 2 Gene Mutation - Inactivating Ras-Related C3 Botulinum Toxin Substrate 2 Gene Mutation - Inactivating p21-Rac2 Gene Mutation - RAC2 Deficiency - RAC2 Deficient - RAC2 Gene Inactivation - RAC2 Inactivating Gene Mutation - RAC2 Inactivating Mutation - RAC2 Loss of Function - RAC2 Loss of Function Gene Mutation - RAC2 Loss of Function Mutation