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Cellosaurus EDi001-A (CVCL_AW97)

[Text version]
Cell line name EDi001-A
Synonyms AST22; AST23
Accession CVCL_AW97
Resource Identification Initiative To cite this cell line use: EDi001-A (RRID:CVCL_AW97)
Comments From: University of Edinburgh; Edinburgh; United Kingdom.
Population: Caucasian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Gene amplification; HGNC; 11138; SNCA; Triplication; Zygosity=Heterozygous (PubMed=21863007).
Disease Parkinson disease 4, autosomal dominant (NCIt: C198604)
Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_F204 (ND27760)
CVCL_LE51 (EDi001-A-1)CVCL_LE52 (EDi001-A-2)CVCL_LE53 (EDi001-A-3)
CVCL_LE54 (EDi001-A-4)CVCL_D0VC (EDi001-A-5)
Sex of cell Female
Age at sampling 55Y
Category Induced pluripotent stem cell

PubMed=21863007; DOI=10.1038/ncomms1453
Devine M.J., Ryten M., Vodicka P., Thomson A.J., Burdon T., Houlden H., Cavaleri F., Nagano M., Drummond N.J., Taanman J.-W., Schapira A.H.V., Gwinn-Hardy K.A., Hardy J., Lewis P.A., Kunath T.
Parkinson's disease induced pluripotent stem cells with triplication of the alpha-synuclein locus.
Nat. Commun. 2:440.1-440.10(2011)

Cell line collections (Providers) EBiSC; EDi001-A
ECACC; 66540058 - Discontinued
Cell line databases/resources hPSCreg; EDi001-A
SKIP; SKIP002512
Biological sample resources BioSamples; SAMEA3319992
Encyclopedic resources Wikidata; Q54831971
Entry history
Entry creation02-May-2016
Last entry update30-Jan-2024
Version number16