ID   FINi004-A
AC   CVCL_C8SQ
SY   PPMI14557.107LRRK2R1441G(het.AAVS1.CAGG.iM.jRCaMP1b)
DR   hPSCreg; FINi004-A
DR   Wikidata; Q123031283
CC   From: The Florey Institute of Neuroscience and Mental Health, University of Melbourne; Melbourne; Australia.
CC   Population: Hispanic.
CC   Sequence variation: Mutation; HGNC; 18618; LRRK2; Simple; p.Arg1441Gly (c.4321C>G); ClinVar=VCV000001936; Zygosity=Heterozygous (from parent cell line).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
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_D5RY ! PPMI.I.1075.1
SX   Female
AG   42Y
CA   Induced pluripotent stem cell
DT   Created: 05-10-23; Last updated: 10-09-24; Version: 4
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