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Human Disease and Mouse Model Detail
Human Disease Myasthenic Syndrome, Congenital, 1a, Slow-Channel; CMS1A
OMIM ID: 601462
Synonyms Cms IIA, Formerly; Myasthenic Syndrome; Myasthenic Syndrome, Congenital, Type IIA, Formerly; CMS2A, FORMERLY
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...
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Chrne* CHRNE   1:1 Homology
     Chrna1 CHRNA1*   1:1 Homology
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Ckm-Chrne*L269F)5Cgz  

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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last database update
05/12/2015
MGI 5.21
The Jackson Laboratory