ID   STBCi067-A
AC   CVCL_D0LV
SY   SFC855-03-08
DR   BioSamples; SAMEA104493800
DR   EBiSC; STBCi067-A
DR   ECACC; 66540795
DR   hPSCreg; STBCi067-A
DR   Wikidata; Q123033560
CC   From: StemBANCC; Oxford; United Kingdom.
CC   Sequence variation: Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (hPSCreg=STBCi067-A).
CC   Discontinued: ECACC; 66540795; true.
CC   Cell type: Fibroblast; CL=CL_0000057.
DI   NCIt; C198605; Parkinson disease 8, autosomal dominant
DI   ORDO; Orphanet_411602; Hereditary late-onset Parkinson disease
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Age unspecified
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 30-01-24; Version: 2
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