| Human Disease |
Usher Syndrome, Type IF; USH1F OMIM ID: 602083 |
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| View all models | View ALL (2) 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 |
| Pcdh15av-Jfb/Pcdh15av-Jfb |
involves: 129X1/SvJ * C57BL/6 | J:84779 | View |
| Pcdh15av-3J/Pcdh15av-3J |
C57BL/6J-Pcdh15av-3J/J | J:95655 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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