| Human Disease |
Hypokalemic Periodic Paralysis, Type 1; HOKPP1 OMIM ID: 170400 |
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| Synonyms | Hypokalemic Periodic Paralysis; HOKPP | |||||||||||||||||||||
| View all models | View ALL (2) 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 |
| Cacna1stm1.1Cann/Cacna1stm1.1Cann |
involves: 129 | J:19367 | View |
| Cacna1stm1.1Cann/Cacna1s+ |
involves: 129 | J:193967 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/08/2013 MGI 5.13 |
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