Home  |  Contact

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; UK.
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-A
ECACC; 66540676
Cell line databases/resources hPSCreg; STBCi019-A
Biological sample resources BioSamples; SAMEA104493637
Gene expression databases GEO; GSM2392421
GEO; GSM2392482
Other Wikidata; Q54956388
Entry history
Entry creation05-Mar-2018
Last entry update20-May-2021
Version number7