ID   UOXFi002-C
AC   CVCL_IJ06
SY   MK082-31
DR   BioSamples; SAMEA7615168
DR   EBiSC; UOXFi002-C
DR   ECACC; 66540390
DR   GEO; GSM2634092
DR   GEO; GSM2644509
DR   hPSCreg; UOXFi002-C
DR   Wikidata; Q54991438
CC   From: University of Oxford; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 4177; GBA; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Heterozygous (EBiSC).
CC   Omics: Transcriptome analysis.
CC   Discontinued: EBiSC; UOXFi002-C; true.
CC   Derived from sampling site: Skin; dermis. Cell type=Fibroblast.
DI   NCIt; C26845; Parkinson's disease
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens
HI   CVCL_A8Y8 ! MK082
SX   Male
AG   51Y
CA   Induced pluripotent stem cell
DT   Created: 01-12-16; Last updated: 17-03-22; Version: 11
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