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Cellosaurus STBCi067-A (CVCL_D0LV)

[Text version]
Cell line name STBCi067-A
Synonyms SFC855-03-08
Accession CVCL_D0LV
Resource Identification Initiative To cite this cell line use: STBCi067-A (RRID:CVCL_D0LV)
Comments From: StemBANCC; Oxford; United Kingdom.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (hPSCreg=STBCi067-A).
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)
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Cell line collections (Providers) EBiSC; STBCi067-A
ECACC; 66540795 - Discontinued
Cell line databases/resources hPSCreg; STBCi067-A
Biological sample resources BioSamples; SAMEA104493800
Encyclopedic resources Wikidata; Q123033560
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2