| Cell line name | HPS2856 |
|---|---|
| Accession | CVCL_D0VX |
| Resource Identification Initiative | To cite this cell line use: HPS2856 (RRID:CVCL_D0VX) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Protein S deficiency disease (NCIt: C99026) Severe hereditary thrombophilia due to congenital protein S deficiency (ORDO: Orphanet_743) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_D0VT ! HPS2852 CVCL_D0VU ! HPS2853 CVCL_D0VV ! HPS2854 CVCL_D0VW ! HPS2855 CVCL_D0VY ! HPS2857 |
| Sex of cell | Female |
| Age at sampling | 70-79Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2856 |
| Encyclopedic resources | Wikidata; Q123032431 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |