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Symbol Name ID |
Myo6
myosin VI MGI:104785 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Congenital stationary night blindness |
Rod-cone dystrophy |
| Disease(s) Associated with MYO6 | ||
| autosomal recessive nonsyndromic deafness 37 |
| Mouse Phenotypes | vision/eye phenotype |
abnormal eye electrophysiology |
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| Availability | Mouse Genotype | ||
| Myo6sv/Myo6sv | * | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/16/2024 MGI 6.23 |
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