Cellosaurus HPSI1016i-eoxu_6 (CVCL_YU06)
| Cell line name | HPSI1016i-eoxu_6 |
|---|---|
| Accession | CVCL_YU06 |
| Resource Identification Initiative | To cite this cell line use: HPSI1016i-eoxu_6 (RRID:CVCL_YU06) |
| 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_YU05 ! HPSI1016i-eoxu_2 |
| Sex of cell | Male |
| Age at sampling | 5-9Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | ECACC; 77650827 |
| Cell line databases/resources | HipSci; HPSI1016i-eoxu_6 |
| Biological sample resources | BioSamples; SAMEA104134230 |
| Encyclopedic resources | Wikidata; Q94235630 |
| Entry history | |
| Entry creation | 12-Mar-2020 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |