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Cellosaurus SF871 (CVCL_A8Z2)

[Text version]
Cell line name SF871
Accession CVCL_A8Z2
Resource Identification Initiative To cite this cell line use: SF871 (RRID:CVCL_A8Z2)
Comments 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=Unspecified (from child cell line STBCi084-A).
Disease Parkinson's disease (NCIt: C26845)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_RD30 (STBCi084-A)CVCL_RD31 (STBCi084-B)CVCL_RD32 (STBCi084-C)
Sex of cell Female
Age at sampling Age unspecified
Category Finite cell line
Cross-references
Encyclopedic resources Wikidata; Q102114911
Gene expression databases GEO; GSM2644519
Entry history
Entry creation29-Oct-2020
Last entry update29-Jun-2023
Version number7