| Cell line name | HPS2125 |
|---|---|
| Accession | CVCL_A3IB |
| Resource Identification Initiative | To cite this cell line use: HPS2125 (RRID:CVCL_A3IB) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Lennox-Gastaut syndrome (NCIt: C84816) Lennox-Gastaut syndrome (ORDO: Orphanet_2382) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_A3HW ! HPS2120 CVCL_A3HX ! HPS2121 CVCL_A3HY ! HPS2122 CVCL_A3HZ ! HPS2123 CVCL_A3IA ! HPS2124 |
| Sex of cell | Male |
| Age at sampling | 20-29Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2125 |
| Encyclopedic resources | Wikidata; Q105508472 |
| Entry history | |
| Entry creation | 12-Jan-2021 |
| Last entry update | 29-Jun-2023 |
| Version number | 4 |