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Cellosaurus UOXFi007-B (CVCL_LE38)

[Text version]
Cell line name UOXFi007-B
Synonyms MK002-6
Accession CVCL_LE38
Resource Identification Initiative To cite this cell line use: UOXFi007-B (RRID:CVCL_LE38)
Comments From: University of Oxford; Oxford; United Kingdom.
Omics: Genome sequenced.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (EBiSC=UOXFi007-B).
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_A8Y3 (MK002)
Sex of cell Female
Age at sampling 72Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; UOXFi007-B - Discontinued
ECACC; 66540549 - Discontinued
Cell line databases/resources hPSCreg; UOXFi007-B
Biological sample resources BioSamples; SAMEA103887562
Encyclopedic resources Wikidata; Q54991455
Entry history
Entry creation22-Aug-2017
Last entry update19-Dec-2024
Version number14