Symbol Name ID |
Scn4a
sodium channel, voltage-gated, type IV, alpha MGI:98250 |
Darker colors indicate more annotations |
Human Phenotypes | Pleural effusion |
Inspiratory stridor |
Neonatal inspiratory stridor |
Apnea |
Respiratory distress |
Pulmonary hypoplasia |
Respiratory insufficiency |
Disease(s) Associated with SCN4A | |||||||
congenital myasthenic syndrome 16 | |||||||
congenital myopathy 22A | |||||||
congenital myopathy 22B | |||||||
hyperkalemic periodic paralysis | |||||||
paramyotonia congenita of Von Eulenburg |
Mouse Phenotypes | abnormal lung volume |
respiratory distress |
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Availability | Mouse Genotype | ||
Scn4am1Aaa/Scn4am1Aaa | |||
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 05/14/2024 MGI 6.23 |
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