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Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Ataxia 1; SCA1
OMIM ID: 164400
Human Phenotype Ontology associations
Synonyms Cerebelloparenchymal Disorder I; CPD1; Menzel Type OPCA; Olivopontocerebellar Atrophy I; OPCA1; Olivopontocerebellar Atrophy IV; OPCA4; OPCA I; Opca IV; Schut-Haymaker Type Opca; Spinocerebellar Ataxia; Spinocerebellar Atrophy I
View all models View ALL (3) 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
     ATXN1* Atxn1* View 3 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(Pcp2-ATXN1*82Q)5Horr View 1 model
  Tg(tetO-ATXN1*82Q)#Horr View 1 model
References Disease References using Mouse Models (12)

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
MGI 6.07
The Jackson Laboratory