| Cell line name | CS2OS hTERT-1 |
|---|---|
| Accession | CVCL_ZY33 |
| Resource Identification Initiative | To cite this cell line use: CS2OS hTERT-1 (RRID:CVCL_ZY33) |
| Comments | Population: Japanese. Transfected with: HGNC; 11730; TERT. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Cockayne syndrome type A (NCIt: C135725) Cockayne syndrome (ORDO: Orphanet_191) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_2881 (CS2OS) |
| Sex of cell | Male |
| Age at sampling | Fetus |
| Category | Telomerase immortalized cell line |
| Cross-references | |
| Cell line collections (Providers) | JCRB; JCRB3065 - Discontinued
JCRB; KURB1904 |
| Encyclopedic resources | Wikidata; Q102113721 |
| Entry history | |
| Entry creation | 29-Oct-2020 |
| Last entry update | 29-Jun-2023 |
| Version number | 6 |