Cellosaurus HPS2125 (CVCL_A3IB)
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 |