| Human Disease |
Usher Syndrome, Type IIC; USH2C OMIM ID: 605472 |
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| 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 |
| Gpr98tm1Pwh/Gpr98tm1Pwh |
involves: 129S1/Sv * C57BL/6J | J:109595 | View |
| Gpr98tm1Msat/Gpr98tm1Msat |
involves: 129P2/OlaHsd * C57BL/6J | J:122415 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Slc4a7tm1Krtz/Slc4a7tm1Krtz |
involves: 129S5/SvEvBrd * C57BL/6 | J:86635 | 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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