| Human Disease |
Angelman Syndrome; AS OMIM ID: 105830 |
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| 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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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Ube3atm1Jwf/Ube3a+ |
B6.129S4-Ube3atm1Jwf | J:75622 | View |
| Ube3atm1Alb/Ube3a+ |
involves: 129S7/SvEvBrd * C57BL/6 | J:50811 | View |
| Ube3atm1Alb/Ube3a+ |
involves: 129S7/SvEvBrd * C57BL/6J | J:190050 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Snrpntm1Kaj/Snrpn+ |
either: 129S1-Snrpntm1Kaj or (involves: 129S1/Sv * C57BL/6J) | J:105412 | 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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