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Cellosaurus UOXFi007-C (CVCL_LE39)

[Text version]
Cell line name UOXFi007-C
Synonyms MK002-7
Accession CVCL_LE39
Resource Identification Initiative To cite this cell line use: UOXFi007-C (RRID:CVCL_LE39)
Comments From: University of Oxford; Oxford; United Kingdom.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Heterozygous (EBiSC=UOXFi007-C).
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-C - Discontinued
ECACC; 66540557 - Discontinued
Cell line databases/resources hPSCreg; UOXFi007-C
Biological sample resources BioSamples; SAMEA103988271
Encyclopedic resources Wikidata; Q54991456
Entry history
Entry creation22-Aug-2017
Last entry update30-Jan-2024
Version number13