Cellosaurus NH50186 (CVCL_UW88)
Cell line name | NH50186 |
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Accession | CVCL_UW88 |
Resource Identification Initiative | To cite this cell line use: NH50186 (RRID:CVCL_UW88) |
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 | Gaucher disease (NCIt: C61268) Parkinson's disease (NCIt: C26845) Gaucher disease (ORDO: Orphanet_355) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602) |
Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
Hierarchy | Parent: CVCL_UW86 (NH50182) |
Sex of cell | Male |
Age at sampling | 65Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | NHCDR; NH50186 |
Encyclopedic resources | Wikidata; Q98127627 |
Entry history | |
Entry creation | 25-Feb-2019 |
Last entry update | 30-Jan-2024 |
Version number | 10 |