Cellosaurus AG03141.hTERT clone 8 (CVCL_B4N4)
| Cell line name | AG03141.hTERT clone 8 |
|---|---|
| Synonyms | AG03141B:pBABE-hTERT clone 8 |
| Accession | CVCL_B4N4 |
| Resource Identification Initiative | To cite this cell line use: AG03141.hTERT clone 8 (RRID:CVCL_B4N4) |
| Comments | Population: Caucasian; Spanish. Genetic integration: Method=Transduction; Gene=HGNC; HGNC:11730; TERT. Genetic integration: Method=Transduction; Gene=UniProtKB; P13249; Streptomyces alboniger pac (PuroR). Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Werner syndrome (NCIt: C3447) Werner syndrome (ORDO: Orphanet_902) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_X767 (AG03141) |
| Sex of cell | Female |
| Age at sampling | 29Y11M |
| Category | Telomerase immortalized cell line |
| Publications | PubMed=10615119; DOI=10.1038/71630 PubMed=16339323; DOI=10.1093/gerona/60.11.1386 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q110432569 |
| Entry history | |
| Entry creation | 16-Dec-2021 |
| Last entry update | 14-Aug-2025 |
| Version number | 7 |