Cellosaurus EDi001-A-5 (CVCL_D0VC)
Cell line name | EDi001-A-5 |
---|---|
Synonyms | AST23-2KO-II8B |
Accession | CVCL_D0VC |
Resource Identification Initiative | To cite this cell line use: EDi001-A-5 (RRID:CVCL_D0VC) |
Comments | From: University of Edinburgh; Edinburgh; United Kingdom. Population: Caucasian. Characteristics: The donor of the original cell line has 4 copies of SNCA. This edited cell line clone has 2 of the 4 alleles KO by CRISPR/Cas9 (hPSCreg=EDi001-A-5). Knockout cell: Method=CRISPR/Cas9; HGNC; 11138; SNCA (Note=2 of 4 alleles). Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620. |
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_AW97 (EDi001-A) |
Sex of cell | Female |
Age at sampling | 55Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | EBiSC; EDi001-A-5
ECACC; 66770006 - Discontinued |
Cell line databases/resources | hPSCreg; EDi001-A-5 |
Biological sample resources | BioSamples; SAMEA7111748 |
Encyclopedic resources | Wikidata; Q123031227 |
Entry history | |
Entry creation | 05-Oct-2023 |
Last entry update | 30-Jan-2024 |
Version number | 2 |