| Cell line name | HPS2298 |
|---|---|
| Synonyms | BRCi020-C |
| Accession | CVCL_YS55 |
| Resource Identification Initiative | To cite this cell line use: HPS2298 (RRID:CVCL_YS55) |
| Comments | Population: Japanese. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | 22q11.2 deletion syndrome (NCIt: C2989) 22q11.2 deletion syndrome (ORDO: Orphanet_567) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_YS53 ! HPS2296 CVCL_YS54 ! HPS2297 CVCL_YS56 ! HPS2299 CVCL_YS57 ! HPS2300 |
| Sex of cell | Male |
| Age at sampling | 1-5Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2298 |
| Cell line databases/resources | hPSCreg; BRCi020-C |
| Encyclopedic resources | Wikidata; Q94220073 |
| Entry history | |
| Entry creation | 12-Mar-2020 |
| Last entry update | 05-Oct-2023 |
| Version number | 6 |