ERCC2 wt Allele

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. (NCI Thesaurus)

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ERCC2 Gene

This gene is involved in nucleotide excision repair and corrects sensitivity to UV radiation and defective nucleotide excision repair in xeroderma pigmentosum…

ERCC1 wt Allele

Human ERCC1 wild-type allele is located within 19q13.2-q13.3 and is approximately 14 kb in length. This allele, which encodes DNA excision repair…

ERCC1 Protein Expression

An immunohistochemical diagnostic test to evaluate the expression of ERCC1 protein at the cellular level.

ERCC1 Gene

This gene is involved in nucleotide excision repair.

ERC1/RET Fusion Protein

A fusion protein encoded by the ERC1/RET fusion gene. This protein is comprised of the N-terminal half of the ELKS/Rab6-interacting/CAST family member…

ERC1/RET Fusion Gene

A fusion gene that results from a chromosomal translocation t(10;12)(q11;p13) which fuses intron 10 of the ERC1 gene to intron 11 of…