About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Ataxia 7; SCA7
OMIM ID: 164500
Human Phenotype Ontology associations
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 (7) 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
     ATXN7* Atxn7* View 7 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(Prnp-ATXN7*92Q)1963Als View 1 model
  Tg(Prnp-ATXN7*92Q)6076Als View 1 model
References Disease References using Mouse Models (7)

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