| Cell line name | HPS2359 |
|---|---|
| Accession | CVCL_UP10 |
| Resource Identification Initiative | To cite this cell line use: HPS2359 (RRID:CVCL_UP10) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Hunter syndrome (NCIt: C61260) Mucopolysaccharidosis type 2 (ORDO: Orphanet_580) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_A3MT ! HPS2360 CVCL_A3MU ! HPS2361 CVCL_A3MV ! HPS2362 CVCL_A3MW ! HPS2363 CVCL_A3MX ! HPS2364 |
| Sex of cell | Male |
| Age at sampling | 10-19Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2359 |
| Encyclopedic resources | Wikidata; Q94220103 |
| Entry history | |
| Entry creation | 25-Feb-2019 |
| Last entry update | 29-Jun-2023 |
| Version number | 6 |