Symbol Name ID |
Scn8a
sodium channel, voltage-gated, type VIII, alpha MGI:103169 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hypotonia |
Disease(s) Associated with SCN8A | |
developmental and epileptic encephalopathy 13 |
Mouse Phenotypes | muscle phenotype |
dystonia |
myoclonus |
myocardial fiber degeneration |
decreased skeletal muscle fiber size |
skeletal muscle necrosis |
dystrophic muscle |
muscle degeneration |
muscular atrophy |
abnormal muscle physiology |
impaired muscle relaxation |
abnormal muscle tone |
muscle weakness |
progressive muscle weakness |
myopathy |
|
Availability | Mouse Genotype | |||||||||||||||
Scn8a6J/Scn8a6J | ||||||||||||||||
Scn8a7J/Scn8a7J | ||||||||||||||||
Scn8a9J/Scn8a9J | ||||||||||||||||
Scn8admu/Scn8admu | ||||||||||||||||
Scn8am11J/Scn8am11J | ||||||||||||||||
Scn8amed-J/Scn8amed-J | ||||||||||||||||
Scn8amed-jo/Scn8amed-jo | * | |||||||||||||||
Scn8amed-TgA4Bs/Scn8amed-TgA4Bs | ||||||||||||||||
Scn8amed/Scn8amed | ||||||||||||||||
Scn8admu/Scn8amed |
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 08/02/2024 MGI 6.24 |
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