| Cell line name | HPS2231 |
|---|---|
| Accession | CVCL_A3QM |
| Resource Identification Initiative | To cite this cell line use: HPS2231 (RRID:CVCL_A3QM) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Spinocerebellar ataxia (NCIt: C82341) Rare hereditary ataxia (ORDO: Orphanet_183518) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_UP03 ! HPS2226 CVCL_A3QI ! HPS2227 CVCL_A3QJ ! HPS2228 CVCL_A3QK ! HPS2229 CVCL_A3QL ! HPS2230 |
| Sex of cell | Male |
| Age at sampling | 80-89Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2231 |
| Encyclopedic resources | Wikidata; Q105508573 |
| Entry history | |
| Entry creation | 12-Jan-2021 |
| Last entry update | 29-Jun-2023 |
| Version number | 4 |