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Cellosaurus STBCi007-A (CVCL_RB41)

[Text version]
Cell line name STBCi007-A
Synonyms SFC855-03-06
Accession CVCL_RB41
Resource Identification Initiative To cite this cell line use: STBCi007-A (RRID:CVCL_RB41)
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; 18618; LRRK2; Simple; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Unspecified (EBiSC=STBCi007-A).
Disease Parkinson disease 8, autosomal dominant (NCIt: C198605)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_RB42 ! STBCi007-B
CVCL_RB43 ! STBCi007-C
Sex of cell Male
Age at sampling Age unspecified
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; STBCi007-A
ECACC; 66540584 - Discontinued
Cell line databases/resources hPSCreg; STBCi007-A
Biological sample resources BioSamples; SAMEA104129752
Encyclopedic resources Wikidata; Q54956337
Entry history
Entry creation05-Mar-2018
Last entry update30-Jan-2024
Version number12