| Cell line name | HPS1915 |
|---|---|
| Accession | CVCL_C9Q3 |
| Resource Identification Initiative | To cite this cell line use: HPS1915 (RRID:CVCL_C9Q3) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | 1p36 deletion syndrome (NCIt: C74983) 1p36 deletion syndrome (ORDO: Orphanet_1606) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_C9Q0 ! HPS1912 CVCL_C9Q1 ! HPS1913 CVCL_C9Q2 ! HPS1914 CVCL_C9Q4 ! HPS1916 CVCL_C9Q5 ! HPS1917 |
| Sex of cell | Male |
| Age at sampling | 10-19Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS1915 |
| Encyclopedic resources | Wikidata; Q123031952 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |