| Human Disease |
Usher Syndrome, Type I; USH1 OMIM ID: 276900 |
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| Synonyms | Us1 | ||||||||||||||||||||||||||||
| View all models | View ALL (11) 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 |
| Myo7ash1/Myo7ash1 |
involves: BALB | J:15554, J:5133 | View |
| Myo7ash1-6J/Myo7ash1-6J |
involves: C57BLKS/J | J:17340 | View |
| Myo7ash1-9J/Myo7ash1-9J |
involves: C3.MRL-Faslpr/J | J:49039 | View |
| Myo7a26SB/Myo7a26SB |
involves: BALB/cRl | J:42644 | View |
| Myo7a3336SB/Myo7a3336SB |
involves: BALB/cRl | J:42644 | View |
| Myo7a4494SB/Myo7a4494SB |
involves: BALB/cRl | J:42644 | View |
| Myo7a816SB/Myo7a816SB |
involves: BALB/cRl | J:42644 | View |
| Myo7apolka/Myo7apolka |
involves: C57BL/6J | J:157102 | View |
| Myo7ash1-11J/Myo7ash1-11J |
129.B6-Myo7ash1-11J | J:181430 | View |
| Myo7a816SB/Myo7a816SB |
involves: BALB/cRl * 47BS/Rl | J:46373 | View |
| Myo7aHdb/Myo7a4626SB |
involves: BALB/c * 47BS/Rl * C3HeB/FeJ * CBA/Ca | J:93998 | 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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