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Human Disease and Mouse Model Detail
Human Disease Mental Retardation and Microcephaly with Pontine and Cerebellar Hypoplasia;
OMIM ID: 300749
Synonyms Mental Retardation, X-Linked, Syndromic; Mental Retardation, X-Linked, Syndromic, Najm Type; MRXSNA; Micpch; Micpch Syndrome
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
     CASK* Cask   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
07/28/2015
MGI 5.22
The Jackson Laboratory