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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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     B3GALNT2* B3galnt2   HomoloGene and HGNC

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
07/21/2015
MGI 5.22
The Jackson Laboratory