Parkinson’s LRRK2 iPSC Cell Line Collection
Parkinson’s LRRK2 iPSC Cell Line Collection
Developed in the Schuele Laboratory at Stanford University School of Medicine, the LRRK2 (ESCAPE) collection contains human induced pluripotent stem cell (iPSC) lines focused on pathogenic LRRK2 gene variants. The series includes homozygous and heterozygous LRRK2 p.G2019S mutants, isogenic derivatives generated by Zinc Finger Nuclease (ZFN) editing (biallelic correction, knockout, and unedited controls), healthy controls, and a unique double-mutant line combining LRRK2 p.G2019S with a PARKIN (PRKN) exon 5 copy-number variation. These lines have been widely adopted and cited in multiple peer-reviewed studies and provide a robust, validated platform for modeling LRRK2-associated PD and evaluating new therapeutic approaches.
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Cell Line | Cell Line Alias | Cell Type | Disease | Genetic Alteration/Mutation | Sex | Age at Collection | Ethnicity | Genetically Related Cell Lines | dbGaP Data |
|---|---|---|---|---|---|---|---|---|---|
Human iPS | Parkinson's Disease | LRRK2, p.G2019S Homozygous | Male | 65 years | Caucasian | No | No | ||
Human iPS | Parkinson's Disease | LRRK2, p.G2019S, Homozygous | Female | 60 years | Caucasian | No | No | ||
Human iPS | Parkinson's Disease | LRRK2, p.G2019S Homozygous | Male | 65 years | Caucasian
| No | No | ||
Human iPS | Parkinson's Disease | LRRK2, p.G2019S, Heterozygous | Male | 74 years | Caucasian | No | No | ||
Human iPS | Parkinson's Disease | LRRK2, p.G2019S, Heterozygous | Male | 74 years | Caucasian | No | No |