ERCC2 wt Allele

Cancer Terms -> Gene -> DNA Repair Gene -> ERCC2 Gene -> ERCC2 wt Allele

ERCC2 wt Allele Definition

Human ERCC2 wild-type allele is located in the vicinity of 19q13.3 and is approximately 19 kb in length. This allele, which encodes TFIIH basal transcription factor complex helicase subunit protein, is involved in transcription-coupled nucleotide excision repair. Defects in this allele can result in three different disorders, xeroderma pigmentosum complementation group D, trichothiodystrophy and Cockayne syndrome.

ERCC2 wt Allele Synonyms

ERCC2 wt Allele, CXPD, EM9, ERCC2, Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 2 (Xeroderma Pigmentosum D) wt Allele, MAG, XP, Group D, XP4, XPD, XPD Gene, XPDC

Terms in ERCC2 wt Allele category

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