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Cellosaurus SUSMi005-A-1.2 (CVCL_C0GT)

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Cell line name SUSMi005-A-1.2
Synonyms SNCA3X 0KO C2
Accession CVCL_C0GT
Resource Identification Initiative To cite this cell line use: SUSMi005-A-1.2 (RRID:CVCL_C0GT)
Comments From: Stanford University School of Medicine; Stanford; USA.
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=Unspecified (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_A4QV (Trpl17)
Sex of cell Male
Age at sampling 48Y
Category Induced pluripotent stem cell
Publications

PubMed=35263701; DOI=10.1016/j.scr.2022.102733
Faria Zafar, Vasavi Nallur Srinivasaraghavan, Max Yang Chen, C. Alejandra Morato Torres, Birgitt Schule;
Isogenic human SNCA gene dosage induced pluripotent stem cells to model Parkinson's disease.
Stem Cell Res. 60:102733-102733(2022)

Cross-references
Cell line databases/resources hPSCreg; SUSMi005-A-1
Biological sample resources BioSamples; SAMEA12312965
Encyclopedic resources Wikidata; Q112930436
Entry history
Entry creation23-Jun-2022
Last entry update19-Dec-2024
Version number5