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Cellosaurus STBCi088-B (CVCL_RD42)

[Text version]

Cell line name STBCi088-B
Synonyms SFC872-03-02
Accession CVCL_RD42
Resource Identification Initiative To cite this cell line use: STBCi088-B (RRID:CVCL_RD42)
Comments From: StemBANCC; United Kingdom.
Sequence variations
  • Mutation; HGNC; 4177; GBA; Simple; p.Leu483Pro (c.1448T>C) (L444P); ClinVar=VCV000004288; Zygosity=Unspecified (EBiSC).
Disease Parkinson's disease (NCIt: C26845)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_RD41 ! STBCi088-A
CVCL_RD43 ! STBCi088-C
Sex of cell Male
Category Induced pluripotent stem cell
Cross-references
Cell line collections EBiSC; STBCi088-B
ECACC; 66540852
Cell line databases/resources hPSCreg; STBCi088-B
Biological sample resources BioSamples; SAMEA104493880
Encyclopedic resources Wikidata; Q54970195
Entry history
Entry creation05-Mar-2018
Last entry update16-Dec-2021
Version number8