wrn protein, mouse

Preferred Label : wrn protein, mouse;

MeSH note : the protein responsible for Werner's syndrome homolog in mice, an inherited disease with clinical symptoms resembling premature aging; RefSeq NM_011721;

MeSH synonym : Werner syndrome protein, mouse;

Registry Number MeSH : EC 5.99.-; EC 3.6.4.12;

Is substance : O;

UNII : EC 3.6.4.12;

Details

Origin ID

C499253;

UMLS CUI

C1567660;

MeSH indexing information
- werner syndrome [MeSH Descriptor]
MeSH term(s) associated for indexing
- RecQ helicases [MeSH Descriptor]
- Werner Syndrome Helicase [MeSH Descriptor]
Record concept(s)
- wrn protein, mouse [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]

Keyword's position in hierarchy(ies) :

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