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Human Disease and Mouse Model Detail
Human Disease Amish Infantile Epilepsy Syndrome
OMIM ID: 609056
Synonyms Epilepsy Syndrome, Infantile-Onset Symptomatic; GM3 Synthase Deficiency; Salt and Pepper Mental Retardation Syndrome
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
     St3gal5 ST3GAL5*   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
10/08/2014
MGI 5.20
The Jackson Laboratory