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Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Ataxia 17; SCA17
OMIM ID: 607136
Synonyms Huntington Disease-Like 4; HDL4; Spinocerebellar Ataxia
View all models View ALL (4) 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
     Tbp TBP*   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-TBP*)69Hmhl View 1 model
  Tg(Prnp-TBP*)71-16Xjl View 1 model
  Tg(Prnp-TBP*)71-27Xjl View 1 model
  Tg(Prnp-TBP*)105Xjl 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
Citing These Resources
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last database update
10/08/2014
MGI 5.20
The Jackson Laboratory