About   Help   FAQ
The MGI survey is now closed.
Thanks for your support!
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      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
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 5.21
The Jackson Laboratory