| Cell line name | HPSI1016i-livl_2 |
|---|---|
| Synonyms | WTSIi664-B; WTSIi682-A |
| Accession | CVCL_LM55 |
| Resource Identification Initiative | To cite this cell line use: HPSI1016i-livl_2 (RRID:CVCL_LM55) |
| Comments | From: Cambridge BioResource; Cambridge; United Kingdom. Population: Caucasian; British. Donor information: Donor is said to be suffering from a 'rare genetic neurological disorder'. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Nervous system disorder (NCIt: C26835) Rare genetic neurological disorder (ORDO: Orphanet_71859) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_LM56 ! HPSI1016i-livl_5 |
| Sex of cell | Male |
| Age at sampling | 10-14Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650793 |
| Cell line databases/resources | HipSci; HPSI1016i-livl_2
hPSCreg; WTSIi664-B |
| Biological sample resources | BioSamples; SAMEA104132164 |
| Encyclopedic resources | Wikidata; Q54891611 |
| Entry history | |
| Entry creation | 15-Nov-2017 |
| Last entry update | 29-Jun-2023 |
| Version number | 10 |