| Cell line name | HPS1627 |
|---|---|
| Accession | CVCL_YS36 |
| Resource Identification Initiative | To cite this cell line use: HPS1627 (RRID:CVCL_YS36) |
| Comments | 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_YS37 ! HPS1628 CVCL_YS38 ! HPS1629 CVCL_YS39 ! HPS1630 CVCL_YS40 ! HPS1631 |
| Sex of cell | Female |
| Age at sampling | <10Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections | RCB; HPS1627 |
| Encyclopedic resources | Wikidata; Q94219799 |
| Entry history | |
| Entry creation | 12-Mar-2020 |
| Last entry update | 02-Jul-2020 |
| Version number | 2 |