| Cell line name | HPS2035 |
|---|---|
| Accession | CVCL_C9VF |
| Resource Identification Initiative | To cite this cell line use: HPS2035 (RRID:CVCL_C9VF) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Sequence variations |
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| Disease | Hypophosphatasia (NCIt: C26798) Hypophosphatasia (ORDO: Orphanet_436) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_C9VA ! HPS2030 CVCL_C9VB ! HPS2031 CVCL_C9VC ! HPS2032 CVCL_C9VD ! HPS2033 CVCL_C9VE ! HPS2034 |
| Sex of cell | Female |
| Age at sampling | 1-5Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2035 |
| Encyclopedic resources | Wikidata; Q123032026 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |