| Cell line name | T21C5 |
|---|---|
| Synonyms | ND50027 |
| Accession | CVCL_1E84 |
| Resource Identification Initiative | To cite this cell line use: T21C5 (RRID:CVCL_1E84) |
| Comments | From: NIH Center for Regenerative Medicine (CRM); Bethesda; USA. Population: Caucasian. Karyotypic information: Lost the third copy of chromosome 21. Derived from site: In situ; Chest, skin; UBERON=UBERON_0001868. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Down syndrome (NCIt: C2993) Down syndrome (ORDO: Orphanet_870) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_X867 (AG06872) |
| Sex of cell | Female |
| Age at sampling | 1Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | NHCDR; ND50027 |
| Cell line databases/resources | SKIP; SKIP001645 |
| Encyclopedic resources | Wikidata; Q54971449 |
| Entry history | |
| Entry creation | 08-Jul-2015 |
| Last entry update | 29-Jun-2023 |
| Version number | 12 |