ID   CENSOi047-A
AC   CVCL_WP54
SY   F226c6
DR   hPSCreg; CENSOi047-A
DR   Wikidata; Q93446792
WW   Provider; Axol; -; https://axolbio.com/shop/disease-models/parkinsons-disease-censoi047-a/
CC   From: Axol Bioscience, Ltd (Censo Biotechnologies); Cambridge; United Kingdom.
CC   Sequence variation: Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Arg1441Cys (c.4321C>T); ClinVar=VCV000001938; Zygosity=Unspecified (Axol).
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)
OI   CVCL_WP55 ! CENSOi047-B
SX   Male
AG   59Y
CA   Induced pluripotent stem cell
DT   Created: 05-07-19; Last updated: 10-04-25; Version: 6
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