Cellosaurus NH50190 (CVCL_UW92)
| Cell line name | NH50190 |
|---|---|
| Accession | CVCL_UW92 |
| Resource Identification Initiative | To cite this cell line use: NH50190 (RRID:CVCL_UW92) |
| Comments | Population: Caucasian. Characteristics: Non-edited control for NH50189 (Cellosaurus=CVCL_UW91). 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_QX26 (ND50051) |
| Sex of cell | Male |
| Age at sampling | 52Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | NHCDR; NH50190 |
| Encyclopedic resources | Wikidata; Q98127631 |
| Entry history | |
| Entry creation | 25-Feb-2019 |
| Last entry update | 19-Dec-2024 |
| Version number | 10 |