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Human Disease and Mouse Model Detail
Human Disease Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome;
OMIM ID: 603387
Synonyms Meg-Pmg-Megacc Syndrome; Megalencephaly, Mega Corpus Callosum, and Complete Lack of Motor Development; Megalencephaly, Polymicrogyria, Mega Corpus Callosum Syndrome; Mpph
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
     Akt3 AKT3*   1:1 Homology
Pik3ca PIK3CA*   1:1 Homology
Pik3r2 PIK3R2*   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
07/23/2014
MGI 5.19
The Jackson Laboratory