Symbol Name ID |
Scn4a
sodium channel, voltage-gated, type IV, alpha MGI:98250 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Death in early adulthood |
Death in infancy |
Neonatal death |
Disease(s) Associated with SCN4A | |||
congenital myopathy 22A | |||
hyperkalemic periodic paralysis |
Mouse Phenotypes | mortality/aging |
decreased survivor rate |
perinatal lethality, complete penetrance |
perinatal lethality, incomplete penetrance |
preweaning lethality, complete penetrance |
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Availability | Mouse Genotype | |||||
Scn4am1Aaa/Scn4am1Aaa | ||||||
Scn4atm1.1Ljh/Scn4atm1.1Ljh | ||||||
Scn4atm1Ljh/Scn4atm1Ljh | ||||||
Scn4atm2b(KOMP)Wtsi/Scn4atm2b(KOMP)Wtsi | ||||||
Scn4am1Aaa/Scn4a+ | * | |||||
Scn4am1Aaa/Scn4atm1.1Ljh |
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 04/30/2024 MGI 6.23 |
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