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Human Disease and Mouse Model Detail
Human Disease Dentatorubral-Pallidoluysian Atrophy; DRPLA
OMIM ID: 125370
Human Phenotype Ontology associations
Synonyms Ataxia, Chorea, Seizures, and Dementia; Haw River Syndrome; HRS; Myoclonic Epilepsy with Choreoathetosis; Naito-Oyanagi Disease; NOD
View all models View ALL (5) 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
     ATN1* Atn1 View 5 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(ATN1*)Q129Stsu View 1 model
  Tg(Eno2-ATN1)3Tx View 1 model
  Tg(Eno2-ATN1)14Tx View 1 model
  Tg(Prnp-ATN1)124Dbo View 1 model
  Tg(Prnp-ATN1)150Dbo View 1 model
References Disease References using Mouse Models (3)

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
MGI 6.07
The Jackson Laboratory