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Cellosaurus STBCi023-A (CVCL_RB76)

[Text version]
Cell line name STBCi023-A
Synonyms SFC829-03-02
Accession CVCL_RB76
Resource Identification Initiative To cite this cell line use: STBCi023-A (RRID:CVCL_RB76)
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; 11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (EBiSC=STBCi023-A).
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_A8X8 (SF829)
Sex of cell Male
Age at sampling 46Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; STBCi023-A
ECACC; 66540685 - Discontinued
Cell line databases/resources hPSCreg; STBCi023-A
Biological sample resources BioSamples; SAMEA104493648
Encyclopedic resources Wikidata; Q54956396
Entry history
Entry creation05-Mar-2018
Last entry update30-Jan-2024
Version number12