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Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Ataxia 2; SCA2
OMIM ID: 183090
Synonyms Cerebellar Degeneration with Slow Eye Movements; Olivopontocerebellar Atrophy II; OPCA2; Olivopontocerebellar Atrophy, Holguin Type; Spinocerebellar Ataxia, Cuban Type; Spinocerebellar Atrophy II; Wadia-Swami Syndrome
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
     Atxn2* ATXN2* View 1 model 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(Pcp2-ATXN2*127Q)#Plt 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