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Cellosaurus ULUNDi002-A (CVCL_RV26)

[Text version]
Cell line name ULUNDi002-A
Synonyms CSC-41C; CSC-41
Accession CVCL_RV26
Resource Identification Initiative To cite this cell line use: ULUNDi002-A (RRID:CVCL_RV26)
Comments From: University of Lund; Lund; Sweden.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (PubMed=29414418).
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 Female
Age at sampling 75Y
Category Induced pluripotent stem cell
STR profile Source(s): PubMed=29414418

Markers:
AmelogeninX
CSF1PO11,13
D5S81810,13
D7S8209,12
D13S3178,9
D16S5398,11
D21S1132.2
TH017,9
TPOX8,11
vWA15,16

Run an STR similarity search on this cell line
Publications

PubMed=29414418; DOI=10.1016/j.scr.2018.01.022
Marote A., Pomeshchik Y., Collin A., Goldwurm S., Lamas N.J., Pinto L., Salgado A.J., Roybon L.
Generation of an induced pluripotent stem cell line (CSC-41) from a Parkinson's disease patient carrying a p.G2019S mutation in the LRRK2 gene.
Stem Cell Res. 28:44-47(2018)

Cross-references
Cell line databases/resources hPSCreg; ULUNDi002-A
Encyclopedic resources Wikidata; Q54990745
Entry history
Entry creation05-Mar-2018
Last entry update29-Jun-2023
Version number9