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Human Disease and Mouse Model Detail
Human Disease Muscular Dystrophy-Dystroglycanopathy (congenital with Mental Retardation), Type B, 3; MDDGB3
OMIM ID: 613151
Synonyms Muscular Dystrophy, Congenital, Pomgnt1-Related; Muscular Dystrophy-Dystroglycanopathy
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
     Pomgnt1 POMGNT1*   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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Send questions and comments to User Support. 		last database update
04/08/2014
MGI 5.17 		The Jackson Laboratory