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Cellosaurus WIBR3_LRRK2_G2019S_315_Homo (CVCL_C7VK)

[Text version]
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, Ezgi O.
Derived from site: In situ; Blastocyst; UBERON=UBERON_0000358.
Cell type: Embryonic stem cell; CL=CL_0002322.
Sequence variations
  • Mutation; HGNC; HGNC:18618; LRRK2; Simple_edited; p.Gly2019Ser (c.6055G>A); ClinVar=VCV000001940; Zygosity=Homozygous; Note=By CRISPR/Cas9 (Direct_author_submission).
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 creation29-Jun-2023
Last entry update19-Dec-2024
Version number5