| Cell line name | HPS1662 |
|---|---|
| Accession | CVCL_C9S2 |
| Resource Identification Initiative | To cite this cell line use: HPS1662 (RRID:CVCL_C9S2) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Sturge-Weber syndrome (NCIt: C3391) Sturge-Weber syndrome (ORDO: Orphanet_3205) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_C9S1 ! HPS1661 CVCL_C9S3 ! HPS1663 CVCL_C9S4 ! HPS1664 CVCL_C9S5 ! HPS1665 CVCL_C9S6 ! HPS1666 |
| Sex of cell | Male |
| Age at sampling | 40-49Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS1662 |
| Encyclopedic resources | Wikidata; Q123031918 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |