| Cell line name | UOXFi007-C |
|---|---|
| Synonyms | MK002-7 |
| Accession | CVCL_LE39 |
| Resource Identification Initiative | To cite this cell line use: UOXFi007-C (RRID:CVCL_LE39) |
| Comments | From: University of Oxford; Oxford; United Kingdom. Derived from sampling site: Skin; dermis. |
| Sequence variations | Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (EBiSC). |
| Disease | Parkinson's disease (NCIt: C26845) 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 | EBiSC; UOXFi007-C - Discontinued
ECACC; 66540557 |
| Cell line databases/resources | hPSCreg; UOXFi007-C |
| Biological sample resources | BioSamples; SAMEA103988271 |
| Encyclopedic resources | Wikidata; Q54991456 |
| Entry history | |
| Entry creation | 22-Aug-2017 |
| Last entry update | 16-Dec-2021 |
| Version number | 9 |