Parkinson’s LRRK2 iPSC Cell Line Collection

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

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