| Human Disease |
Short Qt Syndrome 1; SQT1 OMIM ID: 609620 |
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| View all models | View ALL (1) 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 |
| Kcnh2tm1Hjd/Kcnh2tm1Hjd |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:82249 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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