Cellosaurus cell line iPD-C1 (CVCL

Cross-references
Cell line name	iPD-C1
Accession	CVCL_A4MQ
Resource Identification Initiative	To cite this cell line use: iPD-C1 (RRID:CVCL_A4MQ)
Comments	Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations	Mutation; HGNC; HGNC:18618; LRRK2; Simple; chr12:g.40197315A>G; dbSNP=rs1491923; Zygosity=Unspecified (PubMed=29513666).
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	69Y
Category	Induced pluripotent stem cell
Publications	PubMed=29513666; DOI=10.1371/journal.pone.0192497; PMCID=PMC5841660 Lara Marrone, Christine Bus, David C. Schondorf, Julia Catherine Fitzgerald, Manuela Kubler, Benjamin Schmid, Peter Reinhardt, Lydia Reinhardt, Michela Deleidi, Tanya Levin, Andrea Meixner ...Show all 16 authors... , Barbara Klink, Michael Glatza, Christian Johannes Gloeckner, Thomas Gasser, Jared Sterneckert; Show fewer authors Generation of iPSCs carrying a common LRRK2 risk allele for in vitro modeling of idiopathic Parkinson's disease. PLoS ONE 13:e0192497.1-e0192497.24(2018)
Cell line databases/resources	SKIP; SKIP003176
Encyclopedic resources	Wikidata; Q105509684
Entry history
Entry creation	12-Jan-2021
Last entry update	19-Dec-2024
Version number	7