Cellosaurus SUSMi005-A-1.1 (CVCL_C0GS)
Cell line name | SUSMi005-A-1.1 |
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Synonyms | SNCA3X 0KO C1 |
Accession | CVCL_C0GS |
Resource Identification Initiative | To cite this cell line use: SUSMi005-A-1.1 (RRID:CVCL_C0GS) |
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 |
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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 |
Cross-references | |
Cell line databases/resources | hPSCreg; SUSMi005-A-1 |
Biological sample resources | BioSamples; SAMEA12312965 |
Encyclopedic resources | Wikidata; Q112930435 |
Entry history | |
Entry creation | 23-Jun-2022 |
Last entry update | 19-Dec-2024 |
Version number | 5 |