| Cell line name | HPS2848 |
|---|---|
| Accession | CVCL_YS00 |
| Resource Identification Initiative | To cite this cell line use: HPS2848 (RRID:CVCL_YS00) |
| 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_UP21 ! HPS2846 CVCL_YR99 ! HPS2847 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; HPS2848 |
| Encyclopedic resources | Wikidata; Q94220298 |
| Entry history | |
| Entry creation | 12-Mar-2020 |
| Last entry update | 05-Oct-2023 |
| Version number | 5 |