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Human Disease and Mouse Model Detail
Human Disease Mental Retardation, Autosomal Dominant 20; MRD20
OMIM ID: 613443
Synonyms Chromosome 5q14.3 Deletion Syndrome; Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations
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
     Mef2c MEF2C*   1:1 Homology
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
05/08/2013
MGI 5.13 		The Jackson Laboratory