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Cellosaurus UOXFi002-C (CVCL_IJ06)

[Text version]
Cell line name UOXFi002-C
Synonyms MK082-31
Accession CVCL_IJ06
Resource Identification Initiative To cite this cell line use: UOXFi002-C (RRID:CVCL_IJ06)
Comments From: University of Oxford; Oxford; United Kingdom.
Omics: Transcriptome analysis by microarray.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 4177; GBA1; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Heterozygous (EBiSC).
Disease Parkinson's disease (NCIt: C26845)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A8Y8 (MK082)
Sex of cell Male
Age at sampling 51Y
Category Induced pluripotent stem cell
Cell line collections (Providers) EBiSC; UOXFi002-C - Discontinued
ECACC; 66540390
Cell line databases/resources hPSCreg; UOXFi002-C
Biological sample resources BioSamples; SAMEA7615168
Encyclopedic resources Wikidata; Q54991438
Gene expression databases GEO; GSM2634092
GEO; GSM2644509
Entry history
Entry creation01-Dec-2016
Last entry update29-Jun-2023
Version number14