Cellosaurus FINi005-A (CVCL_C8SR)
| Cell line name | FINi005-A |
|---|---|
| Synonyms | PPMI11555.104SNCA.A53T(AAVS1::CAGG-iM.jRCaMP1b) |
| Accession | CVCL_C8SR |
| Resource Identification Initiative | To cite this cell line use: FINi005-A (RRID:CVCL_C8SR) |
| Comments | From: The Florey Institute of Neuroscience and Mental Health, University of Melbourne; Melbourne; Australia. Population: Caucasian, not Hispanic. Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Sequence variations |
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| Disease | Parkinson disease 1, autosomal dominant (NCIt: C198602) Hereditary late-onset Parkinson disease (ORDO: Orphanet_411602) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_D5SL (PPMI.I.1083.2) |
| Sex of cell | Male |
| Age at sampling | 35Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line databases/resources | hPSCreg; FINi005-A |
| Encyclopedic resources | Wikidata; Q123031284 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 10-Sep-2024 |
| Version number | 3 |