WRN protein, human

Preferred Label : WRN protein, human;

MeSH note : the protein responsible for Werner's syndrome, an inherited disease with clinical symptoms resembling premature aging; a DNA-dependent ATPase and a 3'-5' helicase; possesses exonuclease motifs; RefSeq NM_000553;

MeSH synonym : Werner syndrome helicase, human; RECQL2 protein, human; RECQ3 protein, human;

Registry Number MeSH : EC 3.6.1.-; EC 3.6.4.12;

Is substance : O;

UNII : EC 3.6.4.12;

Details

Origin ID

C098785;

UMLS CUI

C0388246;

Automatic exact mappings (from CISMeF team)
- Fanconi Anemia Group J Protein [NCIt concept]
- Fanconi Anemia Group M Protein [NCIt concept]
- General Transcription and DNA Repair Factor IIH Helicase Subunit XPD [NCIt concept]
- RNA Helicase [NCIt concept]
- TFIIH Basal Transcription Factor Complex Helicase XPB Subunit [NCIt concept]
MeSH indexing information
- werner syndrome [MeSH Descriptor]
MeSH term(s) associated for indexing
- RecQ helicases [MeSH Descriptor]
- Werner Syndrome Helicase [MeSH Descriptor]
- exodeoxyribonucleases [MeSH Descriptor]
Record concept(s)
- WRN protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]
UMLS correspondences (same concept)
- Werner Syndrome ATP-Dependent Helicase [NCIt concept]

Keyword's position in hierarchy(ies) :

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