|
Symbol Name ID |
Myo9a
myosin IXa MGI:107735 |
| Darker colors indicate more annotations |
| Human Phenotypes | Decreased fetal movement |
Feeding difficulties |
Nasal regurgitation |
Poor suck |
Choking episodes |
Weak cry |
Dysphonia |
Hypernasal speech |
| Disease(s) Associated with MYO9A | ||||||||
| congenital myasthenic syndrome |
| Mouse Phenotypes | ataxia |
abnormal gait |
seizures |
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| Availability | Mouse Genotype | |||
| Myo9aem1Atuf/Myo9aem1Atuf | ||||
| Myo9atm1.2Bah/Myo9atm1.2Bah | ||||
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 04/09/2024 MGI 6.23 |
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