Cellosaurus cell line iPD-T1 (CVCL

Cross-references
Cell line name	iPD-T1
Accession	CVCL_A4MN
Resource Identification Initiative	To cite this cell line use: iPD-T1 (RRID:CVCL_A4MN)
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; 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	71Y
Category	Induced pluripotent stem cell
Publications	PubMed=29513666; DOI=10.1371/journal.pone.0192497; PMCID=PMC5841660 Marrone L., Bus C., Schondorf D.C., Fitzgerald J.C., Kubler M., Schmid B., Reinhardt P., Reinhardt L., Deleidi M., Levin T., Meixner A., Klink B., Glatza M., Gloeckner C.J., Gasser T., Sterneckert J. Generation of iPSCs carrying a common LRRK2 risk allele for in vitro modeling of idiopathic Parkinson's disease. PLoS ONE 13:E0192497-E0192497(2018)
Cell line databases/resources	SKIP; SKIP003174
Encyclopedic resources	Wikidata; Q105509690
Entry history
Entry creation	12-Jan-2021
Last entry update	19-Dec-2024
Version number	7