| Cell line name | HPS1551 |
|---|---|
| Accession | CVCL_C9UM |
| Resource Identification Initiative | To cite this cell line use: HPS1551 (RRID:CVCL_C9UM) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Smith-Magenis syndrome (NCIt: C75469) Smith-Magenis syndrome (ORDO: Orphanet_819) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_C9UL ! HPS1550 CVCL_C9UN ! HPS1552 CVCL_C9UP ! HPS1553 CVCL_C9UQ ! HPS1554 CVCL_C9UR ! HPS1555 |
| Sex of cell | Male |
| Age at sampling | 10-19Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS1551 |
| Encyclopedic resources | Wikidata; Q123031843 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |