Cellosaurus 3567 corrected (CVCL_E6LP)
| Cell line name | 3567 corrected |
|---|---|
| Synonyms | 3567 (isogenic correction) |
| Accession | CVCL_E6LP |
| Resource Identification Initiative | To cite this cell line use: 3567 corrected (RRID:CVCL_E6LP) |
| Comments | From: Clinical Biospecimen Imaging and Genetic (C-BIG) Repository, Montreal Neurological Institute, McGill University; Montreal; Canada. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Sequence variations |
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| Disease | Parkinson disease 8, autosomal dominant (NCIt: C198605) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_E6LN (3567) |
| Sex of cell | Female |
| Age at sampling | 64Y |
| Category | Induced pluripotent stem cell |
| Web pages | Provider; C-BIG; -; https://cbigr-open.loris.ca/C-BIG_ipsc_catalog_august_2023.pdf |
| Entry history | |
| Entry creation | 10-Apr-2025 |
| Last entry update | 10-Apr-2025 |
| Version number | 1 |