Cellosaurus SF830 (CVCL_A8X9)
| Cell line name | SF830 | ||
|---|---|---|---|
| Accession | CVCL_A8X9 | ||
| Resource Identification Initiative | To cite this cell line use: SF830 (RRID:CVCL_A8X9) | ||
| Comments | Omics: Transcriptome analysis by microarray. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620. | ||
| Sequence variations |
| ||
| Disease | Parkinson disease 1, autosomal dominant (NCIt: C198602) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602) | ||
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | ||
| Hierarchy | Children:
| ||
| Sex of cell | Male | ||
| Age at sampling | 51Y | ||
| Category | Finite cell line | ||
| Publications | PubMed=28827786; DOI=10.1038/s41598-017-09362-3; PMCID=PMC5567139 | ||
| Cross-references | |||
| Encyclopedic resources | Wikidata; Q102114907 | ||
| Gene expression databases | GEO; GSM2392415 | ||
| Entry history | |||
| Entry creation | 29-Oct-2020 | ||
| Last entry update | 29-Jun-2023 | ||
| Version number | 6 | ||