ID   UOXFi007-B
AC   CVCL_LE38
SY   MK002-6
DR   BioSamples; SAMEA103887562
DR   EBiSC; UOXFi007-B
DR   ECACC; 66540549
DR   hPSCreg; UOXFi007-B
DR   Wikidata; Q54991455
CC   From: University of Oxford; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (EBiSC).
CC   Omics: Genome sequenced.
CC   Discontinued: EBiSC; UOXFi007-B; 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_A8Y3 ! MK002
SX   Female
AG   72Y
CA   Induced pluripotent stem cell
DT   Created: 22-08-17; Last updated: 17-03-22; Version: 10
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