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Cellosaurus EDi008-B (CVCL_LE56)

[Text version]
Cell line name EDi008-B
Synonyms G51D-4; EDIi008-B; EDINi008-B
Accession CVCL_LE56
Resource Identification Initiative To cite this cell line use: EDi008-B (RRID:CVCL_LE56)
Comments From: University of Edinburgh; Edinburgh; United Kingdom.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 11138; SNCA; Simple; p.Gly51Asp (c.152G>A); ClinVar=VCV000097000; Zygosity=Heterozygous (EBiSC=EDi008-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)
Originate from same individual CVCL_LE55 ! EDi008-A
Sex of cell Female
Age at sampling 40-50Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; EDi008-B
ECACC; 66540061 - Discontinued
Cell line databases/resources hPSCreg; EDi008-B
Biological sample resources BioSamples; SAMEA3174606
Encyclopedic resources Wikidata; Q54831978
Entry history
Entry creation22-Aug-2017
Last entry update30-Jan-2024
Version number12