Inactivating ERCC2 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the ERCC2 gene that either inhibits expression or results in the translation of an inactive general transcription and DNA repair factor IIH helicase subunit XPD protein.

**Synonyms:** - ERCC2 Gene Inactivation - ERCC2 Inactivating Gene Mutation - ERCC2 Inactivating Mutation - ERCC2 Loss of Function Gene Mutation - ERCC2 Loss of Function Mutation - Inactivating CXPD Gene Mutation - Inactivating EM9 Gene Mutation - Inactivating ERCC Excision Repair 2, TFIIH Core Complex Helicase Subunit Gene Mutation - Inactivating ERCC2 Mutation - Inactivating Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 Gene Mutation - Inactivating Excision-Repair, Complementing Defective, In Chinese Hamster, 2 Gene Mutation - Inactivating MAG Gene Mutation - Inactivating TTD Gene Mutation - Inactivating TTD1 Gene Mutation - Inactivating XP4 Gene Mutation - Inactivating XPD Gene Mutation - Inactivating XPDC Gene Mutation