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Human Disease and Mouse Model Detail
Human Disease Myasthenic Syndrome, Congenital, Associated with Episodic Apnea
OMIM ID: 254210
Synonyms Cms Ia2; CMS-EA; Congenital Myasthenic Syndrome Type Ia2; CMS1A2; Myasthenia Gravis, Familial Infantile, 2, Formerly; FIMG2, FORMERLY; Myasthenia, Familial Infantile; FIM; Myasthenic Syndrome; Myasthenic Syndrome, Presynaptic, Congenital, Associated with Episodic Apnea
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
     Chat CHAT*   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
09/23/2014
MGI 5.19
The Jackson Laboratory