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Cellosaurus 3439 (CVCL_E6LL)

[Text version]
Cell line name 3439
Accession CVCL_E6LL
Resource Identification Initiative To cite this cell line use: 3439 (RRID:CVCL_E6LL)
Comments From: Clinical Biospecimen Imaging and Genetic (C-BIG) Repository, Montreal Neurological Institute, McGill University; Montreal; Canada.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Arg1441Cys (c.4321C>T); ClinVar=VCV000001938; Zygosity=Unspecified (C-BIG).
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)
Hierarchy Children:
CVCL_E6LM (3439 corrected)
Sex of cell Male
Age at sampling 54Y
Category Induced pluripotent stem cell
Web pages Provider; C-BIG; -; https://cbigr-open.loris.ca/C-BIG_ipsc_catalog_august_2023.pdf
Entry history
Entry creation10-Apr-2025
Last entry update10-Apr-2025
Version number1