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Cellosaurus STBCi019-A (CVCL_RB71)

[Text version]
Cell line name STBCi019-A
Synonyms SFC828-03-06; A53T1.2
Accession CVCL_RB71
Resource Identification Initiative To cite this cell line use: STBCi019-A (RRID:CVCL_RB71)
Comments From: StemBANCC; Oxford; United Kingdom.
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 Parent: CVCL_A8X7 (SF828)
Sex of cell Female
Age at sampling 51Y
Category Induced pluripotent stem cell

PubMed=28827786; DOI=10.1038/s41598-017-09362-3
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)

Cell line collections (Providers) EBiSC; STBCi019-A
ECACC; 66540676 - Discontinued
Cell line databases/resources hPSCreg; STBCi019-A
Biological sample resources BioSamples; SAMEA104493637
Encyclopedic resources Wikidata; Q54956388
Gene expression databases GEO; GSM2392421
GEO; GSM2392482
Entry history
Entry creation05-Mar-2018
Last entry update30-Jan-2024
Version number12