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Cellosaurus STBCi084-B (CVCL_RD31)

[Text version]
Cell line name STBCi084-B
Synonyms SFC871-03-04
Accession CVCL_RD31
Resource Identification Initiative To cite this cell line use: STBCi084-B (RRID:CVCL_RD31)
Comments From: StemBANCC; 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; 4177; GBA1; Simple; p.Asn409Ser (c.1226A>G) (N370S); ClinVar=VCV000004290; Zygosity=Unspecified (EBiSC=STBCi084-B).
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_A8Z2 (SF871)
Sex of cell Female
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Cell line collections (Providers) EBiSC; STBCi084-B
ECACC; 66540841 - Discontinued
Cell line databases/resources hPSCreg; STBCi084-B
Biological sample resources BioSamples; SAMEA104493863
Encyclopedic resources Wikidata; Q54970183
Entry history
Entry creation05-Mar-2018
Last entry update30-Jan-2024
Version number14