| Human Disease |
Epilepsy, Familial Temporal Lobe, 1; ETL1 OMIM ID: 600512 |
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| Synonyms | Epilepsy, Lateral Temporal Lobe, Autosomal Dominant; ADLTE; Epilepsy, Partial, with Auditory Features; ADPEAF | |||||||||||||||||||||
| View all models | View ALL (4) 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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Transgenes and other genome features |
Transgenes and other genome features developed in mice to model this disease.
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Lgi1tm1.1Jkc/Lgi1tm1.1Jkc Tyrc-Brd/Tyrc-Brd |
B6.Cg-Tyrc-Brd Lgi1tm1.1Jkc | J:158715 | View |
| Lgi1tm1Mafu/Lgi1tm1Mafu |
involves: 129S6/SvEvTac * C57BL/6 | J:157578 | View |
| Lgi1tm1.1Ics/Lgi1tm1.1Ics |
involves: 129S2/SvPas * BALB/c * C57BL/6 | J:182795 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Tg(Lgi1*)#Mpan/0 |
Not Specified | J:154129 | 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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