| Human Disease |
Deafness, Autosomal Recessive 7; DFNB7 OMIM ID: 600974 |
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| Synonyms | Deafness, Autosomal Recessive 11; DFNB11 | |||||||||||||||||||||
| View all models | View ALL (6) 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 |
| Tmc1dn/Tmc1dn |
involves: STOCK Grhl3ct * M. m. molossinus | J:22445 | View |
| Tmc1Mhdabth/Tmc1+ |
C3HeB/FeJ | J:86685 | View |
| Tmc1nice/Tmc1nice |
involves: C57BL/6 | J:181985 | View |
| Tmc1baringo/Tmc1baringo |
involves: C57BL/6 | J:181985 | View |
| Tmc1stitch/Tmc1stitch |
involves: C57BL/6 | J:181985 | View |
| Tmc1dn/Tmc1dn |
STOCK Grhl3ct/J | J:236 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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