Cellosaurus UOXFi007-B (CVCL_LE38)
| Cell line name | UOXFi007-B |
|---|---|
| Synonyms | MK002-6 |
| Accession | CVCL_LE38 |
| Resource Identification Initiative | To cite this cell line use: UOXFi007-B (RRID:CVCL_LE38) |
| Comments | From: University of Oxford; Oxford; United Kingdom. Omics: Genomics; Whole genome sequencing. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Parkinson disease 8, autosomal dominant (NCIt: C198605) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_A8Y3 (MK002) |
| Sex of cell | Female |
| Age at sampling | 72Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | EBiSC; UOXFi007-B - Discontinued
ECACC; 66540549 - Discontinued |
| Cell line databases/resources | hPSCreg; UOXFi007-B |
| Biological sample resources | BioSamples; SAMEA103887562 |
| Encyclopedic resources | Wikidata; Q54991455 |
| Entry history | |
| Entry creation | 22-Aug-2017 |
| Last entry update | 10-Apr-2025 |
| Version number | 15 |