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Cellosaurus H9 NR4A2-eGFP iCas9 LRRK2(G2019S/G2019S) (CVCL_E7GK)

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Cell line name H9 NR4A2-eGFP iCas9 LRRK2(G2019S/G2019S)
Synonyms H9-Nurr1::H2B-GFP-iCas9-LRRK2G2019S/G2019S
Accession CVCL_E7GK
Resource Identification Initiative To cite this cell line use: H9 NR4A2-eGFP iCas9 LRRK2(G2019S/G2019S) (RRID:CVCL_E7GK)
Comments Characteristics: Cell line with robust Dox-inducible expression of Cas9 and an edited homozygous LRRK2 (G2019S) mutation (PubMed=38917806).
Characteristics: Using CRISPR/Cas9 a P2A-H2B-eGFP-PGKp-PuroR construct was introduced at the C-terminus of NR4A2/NURR1 (from parent cell line).
Characteristics: Using TALEN two constructs SA-2A-HygR-Cas9-TRE and SA-2A-Neo-M2rtTA were introduced in the AAVS1 safe harbor locus, one in each allele (from parent cell line).
Genetic integration: Method=CRISPR/Cas9; Gene=FPbase; R9NL8; eGFP (Note=Enhanced GFP).
Genetic integration: Method=CRISPR/Cas9; Gene=HGNC; HGNC:4761; H2BC11.
Genetic integration: Method=CRISPR/Cas9; Gene=UniProtKB; P13249; S.alboniger pac (PuroR).
Genetic integration: Method=TALEN; Gene=UniProtKB; P00557; Escherichia coli hygromycin-B 4-O-kinase (hph) (HygR).
Genetic integration: Method=TALEN; Gene=UniProtKB; Q99ZW2; Streptomyces pyogenes Cas9.
Genetic integration: Method=TALEN; Gene=UniProtKB; P00552; Transposon Tn5 neo.
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 (PubMed=38917806).
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_E7GJ (H9 NR4A2-eGFP iCas9)
Sex of cell Female
Age at sampling Blastocyst stage
Category Embryonic stem cell
Publications

PubMed=38917806; DOI=10.1016/j.stem.2024.06.001; PMCID=PMC11405001
Saurat N., Minotti A.P., Rahman M.T., Sikder T., Zhang C., Cornacchia D., Jungverdorben J., Ciceri G., Betel D., Studer L.P.
Genome-wide CRISPR screen identifies neddylation as a regulator of neuronal aging and AD neurodegeneration.
Cell Stem Cell 31:1162-1174.e8(2024)

Entry history
Entry creation10-Apr-2025
Last entry update10-Apr-2025
Version number1