| Human Disease |
Hyperkalemic Periodic Paralysis; HYPP OMIM ID: 170500 |
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| Synonyms | Adynamia Episodica Hereditaria with or without Myotonia | |||||||||||||||||||||
| View all models | View ALL (4) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Scn4atm1.1Ljh/Scn4atm1.1Ljh |
B6.129S4-Scn4atm1.1Ljh | J:135831 | View |
| Scn4atm1Ljh/Scn4atm1Ljh |
B6.129S4-Scn4atm1Ljh | J:135831 | View |
| Scn4atm1.1Ljh/Scn4a+ |
B6.129S4-Scn4atm1.1Ljh | J:135831 | View |
| Scn4atm1Ljh/Scn4a+ |
B6.129S4-Scn4atm1Ljh | J:135831 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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