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Human Disease and Mouse Model Detail
Human Disease Spinal and Bulbar Muscular Atrophy, X-Linked 1; SMAX1
OMIM ID: 313200
Synonyms Bulbospinal Muscular Atrophy, X-Linked; Bulbospinal Neuronopathy, X-Linked Recessive; XBSN; Kennedy Disease; KD; Kennedy Spinal and Bulbar Muscular Atrophy; Spinal and Bulbar Muscular Atrophy; SBMA
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

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Ar* AR* 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(ACTA1-Ar)141Kyjo View 1 model
  Tg(AR*100Q)#Als View 1 model
  Tg(AR*100Q)C25Als View 1 model
  Tg(AR*100Q)C32Als View 1 model
  Tg(CAG-AR*97Q)7-8Sobu View 1 model
  Tg(Prnp-AR*112Q)#Deme 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