| Cell line name | HPS2098 |
|---|---|
| Accession | CVCL_YR78 |
| Resource Identification Initiative | To cite this cell line use: HPS2098 (RRID:CVCL_YR78) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Sequence variations |
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| Disease | Developmental and epileptic encephalopathy 6A (NCIt: C147071) Dravet syndrome (ORDO: Orphanet_33069) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_UN97 ! HPS2096 CVCL_YR77 ! HPS2097 CVCL_YR79 ! HPS2099 CVCL_YR80 ! HPS2100 CVCL_YR81 ! HPS2101 |
| Sex of cell | Female |
| Age at sampling | 6-9Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2098 |
| Encyclopedic resources | Wikidata; Q94219920 |
| Entry history | |
| Entry creation | 12-Mar-2020 |
| Last entry update | 05-Oct-2023 |
| Version number | 8 |