Cellosaurus iWS229T-13 (CVCL_EQ37)
| Cell line name | iWS229T-13 |
|---|---|
| Synonyms | WS iPSC iWS229 TERT (clone 13) |
| Accession | CVCL_EQ37 |
| Resource Identification Initiative | To cite this cell line use: iWS229T-13 (RRID:CVCL_EQ37) |
| 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: Transcriptome analysis by 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_EQ35 (iWS229) |
| Sex of cell | Male |
| Age at sampling | 25Y |
| Category | Induced pluripotent stem cell |
| Publications | PubMed=24749076; DOI=10.1016/j.stemcr.2014.02.006; PMCID=PMC3986587 |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q54898387 |
| Gene expression databases | GEO; GSM1184296
GEO; GSM1184297 |
| Entry history | |
| Entry creation | 26-Sep-2016 |
| Last entry update | 19-Dec-2024 |
| Version number | 10 |