| Cell line name | HPS1689 |
|---|---|
| Accession | CVCL_C9SN |
| Resource Identification Initiative | To cite this cell line use: HPS1689 (RRID:CVCL_C9SN) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Cri du chat syndrome (NCIt: C34518) Monosomy 5p (ORDO: Orphanet_281) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_C9SJ ! HPS1685 CVCL_C9SK ! HPS1686 CVCL_C9SL ! HPS1687 CVCL_C9SM ! HPS1688 CVCL_C9SP ! HPS1690 |
| Sex of cell | Female |
| Age at sampling | 1-5Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS1689 |
| Encyclopedic resources | Wikidata; Q123031940 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |