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Human Disease and Mouse Model Detail
Human Disease Spinal and Bulbar Muscular Atrophy, X-Linked 1; SMAX1
OMIM ID: 313200
Human Phenotype Ontology associations
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     AR* Ar 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(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
References Disease References using Mouse Models (16)

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