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Cellosaurus EDi001-A-1 (CVCL_LE51)

[Text version]
Cell line name EDi001-A-1
Synonyms AST22-C; AST23-C
Accession CVCL_LE51
Resource Identification Initiative To cite this cell line use: EDi001-A-1 (RRID:CVCL_LE51)
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; HGNC:11138; SNCA; Triplication; Zygosity=Heterozygous (from parent cell line).
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_AW97 (EDi001-A)
Sex of cell Female
Age at sampling 55Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; EDi001-A-1
ECACC; 66540166 - Discontinued
Cell line databases/resources hPSCreg; EDi001-A-1
Biological sample resources BioSamples; SAMEA3323836
Encyclopedic resources Wikidata; Q54831972
Entry history
Entry creation22-Aug-2017
Last entry update19-Dec-2024
Version number16