| Human Disease |
Deafness, Autosomal Dominant 4A; DFNA4A OMIM ID: 600652 |
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| Synonyms | Deafness, Autosomal Dominant 4; DFNA4 | ||||||||||||||||||||||||||||
| View all models | View ALL (1) 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 |
| Ceacam16tm1Wzm/Ceacam16tm1Wzm |
BALB/cJ-Ceacam16tm1Wzm | J:187537 | 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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