Cellosaurus SUSMi005-A-2.1 (CVCL_C0GU)
| Cell line name | SUSMi005-A-2.1 |
|---|---|
| Synonyms | SNCA3X 1KO C1 |
| Accession | CVCL_C0GU |
| Resource Identification Initiative | To cite this cell line use: SUSMi005-A-2.1 (RRID:CVCL_C0GU) |
| Comments | From: Stanford University School of Medicine; Stanford; USA. Population: Caucasian. Knockout cell: Method=CRISPR/Cas9; HGNC; HGNC:11138; SNCA (Note=1 of 4 alleles). Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
|
| 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-2 |
| Biological sample resources | BioSamples; SAMEA12312966 |
| Encyclopedic resources | Wikidata; Q112930437 |
| Entry history | |
| Entry creation | 23-Jun-2022 |
| Last entry update | 19-Dec-2024 |
| Version number | 6 |