| Human Disease |
Epilepsy, Myoclonic Juvenile; EJM OMIM ID: 254770 |
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| Synonyms | Myoclonic Epilepsy, Juvenile; JME; Petit Mal, Impulsive | |||||||||||||||||||||
| 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 |
| Efhc1tm1Kzy/Efhc1tm1Kzy |
B6.129P2-Efhc1tm1Kzy | J:145858 | View |
| Efhc1tm1Kzy/Efhc1+ |
B6.129P2-Efhc1tm1Kzy | J:145858 | 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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