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Cellosaurus FINi004-A (CVCL_C8SQ)

[Text version]
Cell line name FINi004-A
Synonyms PPMI14557.107LRRK2R1441G(het.AAVS1.CAGG.iM.jRCaMP1b)
Accession CVCL_C8SQ
Resource Identification Initiative To cite this cell line use: FINi004-A (RRID:CVCL_C8SQ)
Comments From: The Florey Institute of Neuroscience and Mental Health, University of Melbourne; Melbourne; Australia.
Population: Hispanic.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 18618; LRRK2; Simple; p.Arg1441Gly (c.4321C>G); ClinVar=VCV000001936; Zygosity=Heterozygous (from parent cell line).
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 Parent: CVCL_D5RY (PPMI.I.1075.1)
Sex of cell Female
Age at sampling 42Y
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; FINi004-A
Encyclopedic resources Wikidata; Q123031283
Entry history
Entry creation05-Oct-2023
Last entry update10-Sep-2024
Version number4