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Human Disease and Mouse Model Detail
Human Disease Muscular Dystrophy-Dystroglycanopathy (congenital with Brain and Eye Anomalies), Type A, 11; MDDGA11
OMIM ID: 615181
Synonyms Muscular Dystrophy-Dystroglycanopathy, Type A; Walker-Warburg Syndrome or Muscle-Eye-Brain Disease, B3galnt2-Related
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
     B3galnt2 B3GALNT2*   1:1 Homology

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
12/09/2014
MGI 5.20
The Jackson Laboratory