Cellosaurus iWS797 (CVCL_EQ42)
| Cell line name | iWS797 | |
|---|---|---|
| Synonyms | WS iPSC from AG12797 | |
| Accession | CVCL_EQ42 | |
| Resource Identification Initiative | To cite this cell line use: iWS797 (RRID:CVCL_EQ42) | |
| Comments | Population: Japanese. 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_X769 (AG12797) Children:
| |
| 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; Q54898392 | |
| Gene expression databases | GEO; GSM1184292
GEO; GSM1184293 | |
| Entry history | ||
| Entry creation | 26-Sep-2016 | |
| Last entry update | 10-Apr-2025 | |
| Version number | 9 | |