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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
Human Phenotype Ontology associations
Synonyms Muscular Dystrophy, Congenital, Pomgnt1-Related; Muscular Dystrophy-Dystroglycanopathy, Type B
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
     POMGNT1* Pomgnt1   HomoloGene and HGNC
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
09/20/2016
MGI 6.05 		The Jackson Laboratory