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Cellosaurus ND34392 (CVCL_A9R1)

[Text version]
Cell line name ND34392
Accession CVCL_A9R1
Resource Identification Initiative To cite this cell line use: ND34392 (RRID:CVCL_A9R1)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Homozygous (Coriell=ND34392).
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_A9R0 (ND32948)
Sex of cell Male
Age at sampling 79Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND34392 - Discontinued
Encyclopedic resources Wikidata; Q102114586
Entry history
Entry creation29-Oct-2020
Last entry update19-Dec-2024
Version number8