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Cellosaurus FFF-031 (CVCL_A9Q0)

[Text version]
Cell line name FFF-031
Synonyms FFF0322010
Accession CVCL_A9Q0
Resource Identification Initiative To cite this cell line use: FFF-031 (RRID:CVCL_A9Q0)
Comments 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 (from child cell line ESi039-A).
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 Children:
CVCL_9S12 (ESi039-A)
Sex of cell Male
Age at sampling 48Y
Category Finite cell line
Encyclopedic resources Wikidata; Q102113822
Entry history
Entry creation29-Oct-2020
Last entry update29-Jun-2023
Version number7