| Human Disease |
Epileptic Encephalopathy, Early Infantile, 1; EIEE1 OMIM ID: 308350 |
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| Synonyms | Infantile Epileptic-Dyskinetic Encephalopathy; Infantile Spasm Syndrome, X-Linked 1; ISSX1; Ohtahara Syndrome, X-Linked; West Syndrome, X-Linked; Xmesid | |||||||||||||||||||||
| 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 |
| Arxtm1Gldn/Y Tg(mI56i-cre,EGFP)1Kc/0 |
involves: 129/Sv * C57BL/6 * CD-1 | J:148311 | View |
| Arxtm1Gldn/Arx+ Tg(mI56i-cre,EGFP)1Kc/0 |
involves: 129/Sv * C57BL/6 * CD-1 | J:148311 | View |
| Arxtm1.1Jno/Y |
involves: 129S7/SvEvBrd * C57BL/6J | J:151082 | 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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