ID   SF828
AC   CVCL_A8X7
DR   GEO; GSM2392413
DR   Wikidata; Q102114905
RX   PubMed=28827786;
CC   Sequence variation: Mutation; HGNC; 11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (PubMed=28827786).
CC   Omics: Transcriptome analysis by microarray.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198602; Parkinson disease 1, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   51Y
CA   Finite cell line
DT   Created: 29-10-20; Last updated: 29-06-23; Version: 6
//
RX   PubMed=28827786; DOI=10.1038/s41598-017-09362-3;
RA   Haenseler W., Zambon F., Lee H., Vowles J., Rinaldi F., Duggal G.,
RA   Houlden H., Gwinn-Hardy K.A., Wray S., Luk K.C., Wade-Martins R.,
RA   James W.S., Cowley S.A.;
RT   "Excess alpha-synuclein compromises phagocytosis in iPSC-derived
RT   macrophages.";
RL   Sci. Rep. 7:9003-9003(2017).
//