| Human Disease |
Seizures, Benign Familial Neonatal, 1; BFNS1 OMIM ID: 121200 |
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| View all models | View ALL (5) 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 |
| Kcnq2tm1.1Naas/Kcnq2tm1.1Naas |
B6.129-Kcnq2tm1.1Naas | J:154582 | View |
| Kcnq2tm1.1Naas/Kcnq2tm1.1Naas |
FVB.129-Kcnq2tm1.1Naas | J:154582 | View |
| Kcnq2tm1Hsa/Kcnq2+ |
involves: 129P2/OlaHsd * C57BL/6 | J:62797 | View |
| Kcnq2tm1.1Naas/Kcnq2tm1.1Naas |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:154582 | View |
| Kcnq2tm1.1Naas/Kcnq2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:154582 | 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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