Cellosaurus NH50182 (CVCL_UW86)
| Cell line name | NH50182 | |||
|---|---|---|---|---|
| Accession | CVCL_UW86 | |||
| Resource Identification Initiative | To cite this cell line use: NH50182 (RRID:CVCL_UW86) | |||
| 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_EY99 (ND34263) Children:
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| Sex of cell | Male | |||
| Age at sampling | 65Y | |||
| Category | Induced pluripotent stem cell | |||
| Cross-references | ||||
| Cell line collections (Providers) | NHCDR; NH50182 | |||
| Encyclopedic resources | Wikidata; Q98127621 | |||
| Entry history | ||||
| Entry creation | 25-Feb-2019 | |||
| Last entry update | 30-Jan-2024 | |||
| Version number | 10 | |||