About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Parkinson Disease 1, Autosomal Dominant; PARK1
OMIM ID: 168601
Human Phenotype Ontology associations
Synonyms Parkinson Disease
View all models View ALL (24) 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
     SNCA* Snca* View 23 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(PDGFB-SNCA)4Ema View 1 model
  Tg(PDGFB-SNCA*A53T)8Ema View 1 model
  Tg(Prnp-SNCA*A53T)23Mkle View 1 model
  Tg(Prnp-SNCA*A53T)25Mkle View 1 model
  Tg(Prnp-SNCA*A53T)83Vle View 2 models
  Tg(Prnp-SNCA*A53T)AAub View 2 models
  Tg(SNCA)ARyot View 1 model
  Tg(SNCA*E46K)3Elan View 1 model
  Tg(Snca-SNCA)#Galt View 1 model
  Tg(Th-SNCA*)1702Yosh View 1 model
  Tg(Thy1-SNCA)61Ema View 1 model
  Tg(Thy1-SNCA*A30P)18Pjk View 1 model
  Tg(THY1-SNCA*A53T)M53Sud View 1 model
  Tg(Thy1-SNCA*E57K)16Ema View 1 model
References Disease References using Mouse Models (42)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory