| Cell line name | HPS2297 |
|---|---|
| Synonyms | BRCi020-B |
| Accession | CVCL_YS54 |
| Resource Identification Initiative | To cite this cell line use: HPS2297 (RRID:CVCL_YS54) |
| Comments | Population: Japanese. Derived from sampling site: Peripheral blood. |
| 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_YS55 ! HPS2298 CVCL_YS56 ! HPS2299 CVCL_YS57 ! HPS2300 |
| Sex of cell | Male |
| Age at sampling | <10Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections | RCB; HPS2297 |
| Cell line databases/resources | hPSCreg; BRCi020-B |
| Encyclopedic resources | Wikidata; Q94220068 |
| Entry history | |
| Entry creation | 12-Mar-2020 |
| Last entry update | 23-Jun-2022 |
| Version number | 3 |