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Cellosaurus NH50362 (CVCL_B6IK)

[Text version]
Cell line name NH50362
Accession CVCL_B6IK
Resource Identification Initiative To cite this cell line use: NH50362 (RRID:CVCL_B6IK)
Comments Population: Caucasian.
Sequence variations
  • Mutation; HGNC; HGNC:4177; GBA1; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Heterozygous (NHCDR=NH50362).
Disease Parkinson's disease (NCIt: C26845)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_B6II ! NH50360
CVCL_B6IJ ! NH50361
Sex of cell Male
Age at sampling 71Y8M
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) NHCDR; NH50362
Encyclopedic resources Wikidata; Q112129458
Entry history
Entry creation17-Mar-2022
Last entry update19-Dec-2024
Version number6