Cellosaurus cell line PD-BP19-iPSC (CVCL

Cross-references
Cell line name	PD-BP19-iPSC
Accession	CVCL_JL86
Resource Identification Initiative	To cite this cell line use: PD-BP19-iPSC (RRID:CVCL_JL86)
Comments	From: National Neuroscience Institute; Singapore; Singapore. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations	Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Arg1628Pro (c.4883G>C); ClinVar=VCV000039198; Zygosity=Heterozygous (PubMed=28395802).
Disease	Parkinson disease 8, autosomal dominant (NCIt: C198605) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin	Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell	Male
Age at sampling	59Y
Category	Induced pluripotent stem cell
Publications	PubMed=28395802; DOI=10.1016/j.scr.2016.12.011 Ma D.-R., Zhou W., Ng E.Y.-L., Zeng L., Zhao Y., Tan E.K. Reprogramming of a human induced pluripotent stem cell (iPSC) line from a Parkinson's disease patient with a R1628P variant in the LRRK2 gene. Stem Cell Res. 18:45-47(2017)
Encyclopedic resources	Wikidata; Q54946769
Entry history
Entry creation	15-May-2017
Last entry update	19-Dec-2024
Version number	11