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Cellosaurus SF829 (CVCL_A8X8)

[Text version]
Cell line name SF829
Accession CVCL_A8X8
Resource Identification Initiative To cite this cell line use: SF829 (RRID:CVCL_A8X8)
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:
CVCL_RB76 (STBCi023-A)CVCL_RB77 (STBCi023-B)CVCL_RB78 (STBCi023-C)
Sex of cell Male
Age at sampling 46Y
Category Finite cell line
Publications

PubMed=28827786; DOI=10.1038/s41598-017-09362-3; PMCID=PMC5567139
Haenseler W., Zambon F., Lee H., Vowles J., Rinaldi F., Duggal G., Houlden H., Gwinn-Hardy K.A., Wray S., Luk K.C., Wade-Martins R., James W.S., Cowley S.A.
Excess alpha-synuclein compromises phagocytosis in iPSC-derived macrophages.
Sci. Rep. 7:9003-9003(2017)

Cross-references
Encyclopedic resources Wikidata; Q102114906
Gene expression databases GEO; GSM2392414
Entry history
Entry creation29-Oct-2020
Last entry update19-Dec-2024
Version number7