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Cellosaurus hTERT-WRN2 (CVCL_ZS70)

[Text version]
Cell line name hTERT-WRN2
Accession CVCL_ZS70
Resource Identification Initiative To cite this cell line use: hTERT-WRN2 (RRID:CVCL_ZS70)
Comments Population: Japanese.
Genetic integration: Method=Transduction; Gene=HGNC; HGNC:11730; TERT.
Genetic integration: Method=Transduction; Gene=UniProtKB; P13249; S.alboniger pac (PuroR).
Derived from site: In situ; Thigh, skin; UBERON=UBERON_0004262.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Werner syndrome (NCIt: C3447)
Werner syndrome (ORDO: Orphanet_902)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_U316 (AG12795)
Sex of cell Male
Age at sampling 19Y
Category Telomerase immortalized cell line
Publications

PubMed=10655550; DOI=10.1093/hmg/9.3.403
Ouellette M.M., McDaniel L.D., Wright W.E., Shay J.W., Schultz R.A.
The establishment of telomerase-immortalized cell lines representing human chromosome instability syndromes.
Hum. Mol. Genet. 9:403-411(2000)

Cross-references
Encyclopedic resources Wikidata; Q98126743
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number9