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Human Disease and Mouse Model Detail
Human Disease Myasthenic Syndrome, Congenital, 4a, Slow-Channel; CMS4A
OMIM ID: 605809
Synonyms Cms Ia1, Formerly; Congenital Myasthenic Syndrome Type Ia1, Formerly; CMS1A1, FORMERLY; Myasthenic Syndrome, Congenital
View all models View ALL (2) mouse models for this human disease.
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
     CHRNE* Chrne* View 2 models HomoloGene
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 View 1 model
References Disease References using Mouse Models (2)

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