ERCC3 wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human ERCC3 wild-type allele is located within 2q21 and is approximately 37 kb in length. This allele, which encodes TFIIH basal transcription factor complex helicase XPB subunit protein, plays a role in nucleotide excision repair and transcription.

**Synonyms:** - BTF2 - BTF2-p89 Gene - Basic Transcription Factor 2 89 kDa Subunit Gene - ERCC Excision Repair 3, TFIIH Core Complex Helicase Subunit wt Allele - Excision Repair Cross-Complementation Group 3 Gene - Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 3 (Xeroderma Pigmentosum Group B Complementing) Gene - Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 3 Gene - Excision-Repair, Complementing Defective, In Chinese Hamster, 3 Gene - Excision-Repair, Complementing Defective, in Chinese Hamster, 3 Gene - GTF2H - RAD25 - TFIIH - TFIIH 89 kDa Subunit Gene - TFIIH Basal Transcription Factor Complex Helicase XPB Subunit Gene - XPB - XPBC - Xeroderma Pigmentosum Group B Complementing Gene