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Human Disease and Mouse Model Detail
Human Disease Myasthenic Syndrome, Congenital, 13; CMS13
OMIM ID: 614750
Synonyms Myasthenic Syndrome, Congenital, with Tubular Aggregates; Myasthenic Syndrome, Congenital, with Tubular Aggregates 2; CMSTA2
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
     DPAGT1* Dpagt1   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