Monoallelic RAD51 Gene Inactivation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** Any gain, loss, or exchange of DNA that results in monoallelic loss of function mutations in the RAD51 gene.

**Synonyms:** - Monoallelic BRCC5 Gene Inactivation - Monoallelic FANCR Gene Inactivation - Monoallelic HRAD51 Gene Inactivation - Monoallelic HsRad51 Gene Inactivation - Monoallelic Inactivating RAD51 Gene Mutation - Monoallelic Inactivating RAD51 Mutation - Monoallelic RAD51 Inactivating Gene Mutation - Monoallelic RAD51 Inactivating Mutation - Monoallelic RAD51 Inactivation - Monoallelic RAD51 Loss of Function - Monoallelic RAD51 Loss of Function Gene Mutation - Monoallelic RAD51 Loss of Function Mutation - Monoallelic RAD51 Recombinase Gene Inactivation - Monoallelic RAD51A Gene Inactivation - Monoallelic RECA Gene Inactivation - RAD51 Gene LOH - RAD51 Homozygous Loss - RAD51 Loss of Heterozygosity