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Human Disease and Mouse Model Detail
Human Disease Parkinson Disease 2, Autosomal Recessive Juvenile; PARK2
OMIM ID: 600116
Human Phenotype Ontology associations
Synonyms Parkinson Disease; Parkinson Disease, Juvenile, Autosomal Recessive; PDJ; Parkinsonism, Early-Onset, with Diurnal Fluctuation; EPDF
View all models View ALL (10) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PARK2* Park2* View 10 models HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Slc6a3-PARK2*Q311X)AXwy View 1 model
References Disease References using Mouse Models (14)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/29/2016
MGI 6.06
The Jackson Laboratory