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Cellosaurus STBCi019-B (CVCL_RB72)

[Text version]
Cell line name STBCi019-B
Synonyms SFC828-03-09
Accession CVCL_RB72
Resource Identification Initiative To cite this cell line use: STBCi019-B (RRID:CVCL_RB72)
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; HGNC:11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (EBiSC=STBCi019-B).
Disease Parkinson disease 1, autosomal dominant (NCIt: C198602)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_A8X7 (SF828)
Sex of cell Female
Age at sampling 51Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; STBCi019-B - Discontinued
ECACC; 66540677 - Discontinued
Cell line databases/resources hPSCreg; STBCi019-B
Biological sample resources BioSamples; SAMEA104493639
Encyclopedic resources Wikidata; Q54956389
Entry history
Entry creation05-Mar-2018
Last entry update19-Dec-2024
Version number13