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Cellosaurus STBCi019-C (CVCL_RB73)

[Text version]

Cell line name STBCi019-C
Synonyms SFC828-03-04; A53T1.1
Accession CVCL_RB73
Resource Identification Initiative To cite this cell line use: STBCi019-C (RRID:CVCL_RB73)
Comments From: StemBANCC; United Kingdom.
Omics: Transcriptome analysis.
Derived from sampling site: Skin; dermis.
Sequence variations Mutation; HGNC; 11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (PubMed=28827786).
Disease Parkinson's disease (NCIt: C26845)
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
Publications

PubMed=28827786; DOI=10.1038/s41598-017-09362-3
Haenseler W., Zambon F., Lee H., Vowles J., Rinaldi F., Duggal G., Houlden H., Gwinn K., 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
Cell line collections EBiSC; STBCi019-C
ECACC; 66540678
Cell line databases/resources hPSCreg; STBCi019-C
Biological sample resources BioSamples; SAMEA104493708
Encyclopedic resources Wikidata; Q54956392
Gene expression databases GEO; GSM2392420
GEO; GSM2392481
Entry history
Entry creation05-Mar-2018
Last entry update16-Dec-2021
Version number8