
Developed in collaboration with the Michael J Fox Foundation, this model contains a deletion of the Park7 (Parkinson disease [autosomal recessive, early onset] 7) gene, also known as DJ-1.
In humans, loss of function of Park7 leads to a form of early-onset Parkinson's disease. This occurs due to the role Park7 plays in protecting neurons from oxidative stress and cell death, making this an ideal model for the study of Parkinson's disease.