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Human Disease and Mouse Model Detail
Human Disease Paroxysmal Nonkinesigenic Dyskinesia 1; PNKD1
OMIM ID: 118800
Synonyms Choreoathetosis, Familial Paroxysmal; FPD1; Choreoathetosis, Nonkinesigenic; Dystonia 8; DYT8; Mount-Reback Syndrome; Paroxysmal Dystonic Choreoathetosis; PDC
View all models View ALL (2) mouse models for this human disease.
Genes and
mouse models 		Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Pnkd PNKD*   1:1 Homology
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(Pnkd*A7V*A9V,-DsRed)671Ljp View 1 model
  Tg(Pnkd*A7V*A9V,-DsRed)704Ljp View 1 model
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
05/08/2013
MGI 5.13 		The Jackson Laboratory