ID   UOXFi007-C
AC   CVCL_LE39
SY   MK002-7
DR   BioSamples; SAMEA103988271
DR   EBiSC; UOXFi007-C
DR   ECACC; 66540557
DR   hPSCreg; UOXFi007-C
DR   Wikidata; Q54991456
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=UOXFi007-C).
CC   Discontinued: EBiSC; UOXFi007-C; true.
CC   Discontinued: ECACC; 66540557; true.
CC   Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C198605; Parkinson disease 8, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_A8Y3 ! MK002
SX   Female
AG   72Y
CA   Induced pluripotent stem cell
DT   Created: 22-08-17; Last updated: 30-01-24; Version: 13
//