About   Help   FAQ
Symbol
Name
ID
Scn4a
sodium channel, voltage-gated, type IV, alpha
MGI:98250
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Decreased fetal movement
Feeding difficulties
Feeding difficulties in infancy
Tube feeding
Bowel incontinence
Weak cry
Hypernasal speech
Fatigue
Chest pain
Myalgia
Disease(s) Associated with SCN4A
congenital myopathy 22A
congenital myopathy 22B
hyperkalemic periodic paralysis
paramyotonia congenita of Von Eulenburg

Mouse Phenotypes
limb grasping
impaired coordination
abnormal grip strength
akinesia
Availability Mouse Genotype
Scn4atm1.1Ljh/Scn4atm1.1Ljh
Scn4atm1Ljh/Scn4atm1Ljh
Scn4am1Aaa/Scn4a+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory