| Cell line name | HPS1725 |
|---|---|
| Accession | CVCL_VM81 |
| Resource Identification Initiative | To cite this cell line use: HPS1725 (RRID:CVCL_VM81) |
| Comments | Population: Japanese. 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) |
| Sex of cell | Female |
| Age at sampling | 20-29Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS1725 |
| Encyclopedic resources | Wikidata; Q94219828 |
| Entry history | |
| Entry creation | 07-Sep-2018 |
| Last entry update | 29-Jun-2023 |
| Version number | 5 |