| Human Disease |
Epilepsy, Juvenile Myoclonic, Susceptibility to, 5; EJM5 OMIM ID: 611136 |
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| 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 |
| Gabra1tm1.1Geh/Gabra1+ |
B6.129(Cg)-Gabra1tm1.1Geh | J:186685 | View |
| Gabra1tm1.1Geh/Gabra1+ |
D2.129(Cg)-Gabra1tm1.1Geh | J:186685 | 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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