Cellosaurus iWS797T (CVCL_EQ43)
| Cell line name | iWS797T |
|---|---|
| Synonyms | WS iPSC iWS797 TERT |
| Accession | CVCL_EQ43 |
| Resource Identification Initiative | To cite this cell line use: iWS797T (RRID:CVCL_EQ43) |
| Comments | Population: Japanese. Genetic integration: Method=Transduction; Gene=HGNC; HGNC:11730; TERT. Genetic integration: Method=Transduction; Gene=UniProtKB; P00557; Escherichia coli hygromycin-B 4-O-kinase (hph) (HygR). Omics: Transcriptomics; Microarray. 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_EQ42 (iWS797) |
| Sex of cell | Male |
| Age at sampling | 36Y |
| Category | Induced pluripotent stem cell |
| Publications | PubMed=24749076; DOI=10.1016/j.stemcr.2014.02.006; PMCID=PMC3986587 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q54898393 |
| Gene expression databases | GEO; GSM1184300
GEO; GSM1184301 |
| Entry history | |
| Entry creation | 26-Sep-2016 |
| Last entry update | 10-Apr-2025 |
| Version number | 10 |