| Human Disease |
Usher Syndrome, Type IIIA; USH3A OMIM ID: 276902 |
|||||||||||||||||||||
| Synonyms | Usher Syndrome, Type III; USH3 | |||||||||||||||||||||
| View all models | View ALL (2) mouse models for this human disease. | |||||||||||||||||||||
|
Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
|
|||||||||||||||||||||
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Clrn1tm1.1Kuna/Clrn1tm1.1Kuna |
involves: C57BL/6J | J:150215 | View |
| Clrn1tm2.1Kuna/Clrn1tm2.1Kuna |
involves: 129 * BALB/cJ * C57BL/6J | J:186316 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
||
|
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support. |
last database update 05/22/2013 MGI 5.13 |
|
|
|
||