Symbol Name ID |
Scn4a
sodium channel, voltage-gated, type IV, alpha MGI:98250 |
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 |
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Availability | Mouse Genotype | ||||
Scn4atm1.1Ljh/Scn4atm1.1Ljh | |||||
Scn4atm1Ljh/Scn4atm1Ljh | |||||
Scn4am1Aaa/Scn4a+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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