Structured Summary
Abstract
A DNA helicase that is a component of TRANSCRIPTION FACTOR TFIIH. It plays an essential role in NUCLEOTIDE EXCISION REPAIR, and mutations in this protein are associated with XERODERMA PIGMENTOSUM.
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Synonyms
4 entry terms
- ERCC2 Protein
- Excision Repair Cross-Complementing Rodent Repair Deficiency, Group 2 Protein
- Xeroderma Pigmentosum Complementation Group D Protein
- Excision Repair Cross Complementing Rodent Repair Deficiency, Group 2 Protein
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2006(1992)
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References
- National Library of Medicine. Xeroderma Pigmentosum Group D Protein. Medical Subject Headings (MeSH). 2026. Unique ID D051759. http://id.nlm.nih.gov/mesh/2026/D051759
- Xeroderma Pigmentosum Group D Protein. In: Wikipedia. https://en.wikipedia.org/wiki/ERCC2
- Xeroderma Pigmentosum Group D Protein. In: Wikidata. https://www.wikidata.org/wiki/Q426168