ID   SY90575
AC   CVCL_VI16
DR   Wikidata; Q54971285
RX   PubMed=9230208;
CC   Sequence variation: Mutation; HGNC; HGNC:12791; WRN; Simple; p.Gln1165Ter (c.3493C>T); ClinVar=VCV000005445; Zygosity=Homozygous (PubMed=9230208).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Transformed cell line
DT   Created: 14-05-18; Last updated: 19-12-24; Version: 9
//
RX   PubMed=9230208;
RA   Bennett S.E., Umar A., Oshima J., Monnat R.J. Jr., Kunkel T.A.;
RT   "Mismatch repair in extracts of Werner syndrome cell lines.";
RL   Cancer Res. 57:2956-2960(1997).
//