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Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Ataxia 7; SCA7
OMIM ID: 164500
Synonyms ADCA, Type II; Autosomal Dominant Cerebellar Ataxia, Type II; Olivopontocerebellar Atrophy III; OPCA3; OPCA III; OPCA with Macular Degeneration and External Ophthalmoplegia; OPCA with Retinal Degeneration; Spinocerebellar Ataxia
View all models View ALL (6) 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
     Atxn7* ATXN7* View 5 models 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(SCA7)c92QAls View 1 model

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
04/08/2014
MGI 5.17
The Jackson Laboratory