| Human Disease |
Myoclonic Epilepsy of Lafora OMIM ID: 254780 |
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| Synonyms | Epilepsy, Progressive Myoclonic 2A; EPM2A; Lafora Body Disease; LBD; Lafora Disease; MELF | |||||||||||||||||||||||||
| View all models | View ALL (3) 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 |
| Epm2atm1Kzy/Epm2atm1Kzy |
involves: 129P2/OlaHsd * C57BL/6J | J:76688, J:173769 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg |
involves: C57BL/6J * C57BL/6NTac | J:165994 | View |
| Nhlrc1tm1.2Geno/Nhlrc1tm1.2Geno |
involves: 129S2/SvPas * C57BL/6J | J:181559 | 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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