| Cell line name | ND50051 | ||
|---|---|---|---|
| Accession | CVCL_QX26 | ||
| Resource Identification Initiative | To cite this cell line use: ND50051 (RRID:CVCL_QX26) | ||
| Comments | Population: Caucasian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. 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_DD50 (ND29802) Children:
| ||
| Sex of cell | Male | ||
| Age at sampling | 52Y | ||
| Category | Induced pluripotent stem cell | ||
| Cross-references | |||
| Cell line collections (Providers) | NHCDR; ND50051 | ||
| Encyclopedic resources | Wikidata; Q54930273 | ||
| Entry history | |||
| Entry creation | 15-Nov-2017 | ||
| Last entry update | 30-Jan-2024 | ||
| Version number | 12 | ||