Cellosaurus cell line STBCi023-B (CVCL_RB77)

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Cell line name	STBCi023-B
Synonyms	SFC829-03-04; A53T2.1
Accession	CVCL_RB77
Resource Identification Initiative	To cite this cell line use: STBCi023-B (RRID:CVCL_RB77)
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	Mutation; HGNC; 11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (PubMed=28827786).
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_A8X8 (SF829)
Sex of cell	Male
Age at sampling	46Y
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-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; STBCi023-B ECACC; 66540686 - Discontinued
Cell line databases/resources	hPSCreg; STBCi023-B
Biological sample resources	BioSamples; SAMEA104493650
Encyclopedic resources	Wikidata; Q54956397
Gene expression databases	GEO; GSM2392422 GEO; GSM2392483
Entry history
Entry creation	05-Mar-2018
Last entry update	30-Jan-2024
Version number	12