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Cellosaurus ND50086 (CVCL_RY37)

[Text version]
Cell line name ND50086
Accession CVCL_RY37
Resource Identification Initiative To cite this cell line use: ND50086 (RRID:CVCL_RY37)
Comments Population: Caucasian; Greek.
Characteristics: Non-edited control for NH50085 (Cellosaurus=CVCL_RY36).
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 11138; SNCA; Simple; p.Ala53Thr (c.157G>A); ClinVar=VCV000014007; Zygosity=Heterozygous (NHCDR=ND50086).
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)
Hierarchy Parent: CVCL_RY35 (ND50050)
Sex of cell Female
Age at sampling 51Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) NHCDR; ND50086
Encyclopedic resources Wikidata; Q54930314
Entry history
Entry creation14-May-2018
Last entry update30-Jan-2024
Version number11