| Human Disease |
Usher Syndrome, Type Ic; USH1C OMIM ID: 276904 |
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| Synonyms | Usher Syndrome, Type I, Acadian Variety | |||||||||||||||||||||
| 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 |
| Ush1cdfcr-2J/Ush1cdfcr-2J |
B6;129S4 | J:85400 | View |
| Ush1cdfcr/Ush1cdfcr |
involves: BALB/cByJ | J:85400 | View |
| Ush1ctm1Bkts/Ush1ctm1Bkts |
involves: 129S6/SvEvTac * C57BL/6J * FVB/N | J:118248 | View |
| Ush1cdfcr-3J/Ush1cdfcr-3J |
STOCK Ush1cdfcr-3J/J | J:147859 | 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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