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Human Disease and Mouse Model Detail
Human Disease Myasthenic Syndrome, Congenital, Associated with Acetylcholine Receptor Deficiency
OMIM ID: 608931
Synonyms Myasthenic Syndrome; Myasthenic Syndrome, Congenital, Postsynaptic, Associated with Acetylcholine Receptor Deficiency; Myasthenic Syndrome, Congenital, Type ID; CMS1D
View all models View ALL (4) mouse models for this human disease.
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
     Chrne* CHRNE* View 1 model 1:1 Homology
Musk* MUSK* View 3 models 1:1 Homology
     Chrnb1 CHRNB1*   1:1 Homology
Gfpt1 GFPT1*   1:1 Homology
Rapsn RAPSN*   1:1 Homology
References Disease References using Mouse Models (3)

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
11/11/2014
MGI 5.20
The Jackson Laboratory