Inactivating ERCC3 Gene Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A change in the nucleotide sequence of the ERCC3 gene that either inhibits expression or results in the translation of an inactive TFIIH basal transcription factor complex helicase XPB subunit protein.

**Synonyms:** - ERCC3 Gene Inactivation - ERCC3 Inactivating Gene Mutation - ERCC3 Inactivating Mutation - ERCC3 Loss of Function Gene Mutation - ERCC3 Loss of Function Mutation - Inactivating BTF2 Gene Mutation - Inactivating ERCC Excision Repair 3, TFIIH Core Complex Helicase Subunit Gene Mutation - Inactivating ERCC3 Mutation - Inactivating Excision Repair Cross-Complementation Group 3 Gene Mutation - Inactivating Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 3 Gene Mutation - Inactivating Excision-Repair, Complementing Defective, in Chinese Hamster, 3 Gene Mutation - Inactivating GTF2H Gene Mutation - Inactivating RAD25 Gene Mutation - Inactivating TTD2 Gene Mutation - Inactivating XPB Gene Mutation - Inactivating Xeroderma Pigmentosum Group B Complementing Gene Mutation