Symbol Name ID |
Scn4a
sodium channel, voltage-gated, type IV, alpha MGI:98250 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased activity of mitochondrial complex I |
Abnormal blood potassium concentration |
Hyperkalemia |
Hypokalemia |
Hyponatremia |
Elevated circulating creatine kinase concentration |
Mildly elevated creatine kinase |
Nonimmune hydrops fetalis |
Pleural effusion |
Malignant hyperthermia |
Ascites |
Disease(s) Associated with SCN4A | |||||||||||
congenital myopathy 22A | |||||||||||
congenital myopathy 22B | |||||||||||
hyperkalemic periodic paralysis | |||||||||||
paramyotonia congenita of Von Eulenburg |
Mouse Phenotypes | decreased circulating leptin level |
decreased circulating alkaline phosphatase level |
increased circulating amylase level |
increased energy expenditure |
improved glucose tolerance |
|
Availability | Mouse Genotype | |||||
Scn4am1Aaa/Scn4a+ | ||||||
Scn4atm2b(KOMP)Wtsi/Scn4a+ |
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 05/07/2024 MGI 6.23 |
|
|