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Cellosaurus NH50358 (CVCL_B6IH)

[Text version]
Cell line name NH50358
Accession CVCL_B6IH
Resource Identification Initiative To cite this cell line use: NH50358 (RRID:CVCL_B6IH)
Comments Population: Caucasian.
Sequence variations
  • Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (NHCDR=NH50358).
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)
Originate from same individual CVCL_B6IG ! NH50357
Sex of cell Male
Age at sampling 81Y5M
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) NHCDR; NH50358
Encyclopedic resources Wikidata; Q112129454
Entry history
Entry creation17-Mar-2022
Last entry update19-Dec-2024
Version number6