Cellosaurus WIBR3_LRRK2_G2019S_315_Homo (CVCL_C7VK)
| Cell line name | WIBR3_LRRK2_G2019S_315_Homo |
|---|---|
| Accession | CVCL_C7VK |
| Resource Identification Initiative | To cite this cell line use: WIBR3_LRRK2_G2019S_315_Homo (RRID:CVCL_C7VK) |
| Comments | Miscellaneous: Cell line not distributed because it failed quality controls (Direct_author_submission). Miscellaneous: Cell line information from personal communication of Booth E. Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358. Cell type: Embryonic stem cell; CL=CL_0002322. |
| 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_9767 (WIBR3) |
| Sex of cell | Female |
| Age at sampling | Blastocyst stage |
| Category | Embryonic stem cell |
| Cross-references | |
| Encyclopedic resources | Wikidata; Q123033873 |
| Entry history | |
| Entry creation | 29-Jun-2023 |
| Last entry update | 02-May-2024 |
| Version number | 3 |