| Cell line name | HPS2846 |
|---|---|
| Accession | CVCL_UP21 |
| Resource Identification Initiative | To cite this cell line use: HPS2846 (RRID:CVCL_UP21) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Prader-Willi syndrome (NCIt: C75463) Prader-Willi syndrome (ORDO: Orphanet_739) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_YR99 ! HPS2847 CVCL_YS00 ! HPS2848 CVCL_YS01 ! HPS2849 CVCL_YS02 ! HPS2850 CVCL_YS03 ! HPS2851 |
| Sex of cell | Female |
| Age at sampling | 6-9Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2846 |
| Encyclopedic resources | Wikidata; Q94220291 |
| Entry history | |
| Entry creation | 25-Feb-2019 |
| Last entry update | 05-Oct-2023 |
| Version number | 6 |