| Cell line name | UOXFi002-B |
|---|---|
| Synonyms | MK082-30 |
| Accession | CVCL_IJ05 |
| Resource Identification Initiative | To cite this cell line use: UOXFi002-B (RRID:CVCL_IJ05) |
| Comments | From: University of Oxford; Oxford; United Kingdom. Derived from sampling site: Skin; dermis. |
| Sequence variations | Mutation; HGNC; 4177; GBA; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; 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_A8Y8 (MK082) |
| Sex of cell | Male |
| Age at sampling | 51Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections | EBiSC; UOXFi002-B
ECACC; 66540389 |
| Cell line databases/resources | hPSCreg; UOXFi002-B |
| Biological sample resources | BioSamples; SAMEA4458549 |
| Encyclopedic resources | Wikidata; Q54991437 |
| Entry history | |
| Entry creation | 01-Dec-2016 |
| Last entry update | 16-Dec-2021 |
| Version number | 10 |