|
Symbol Name ID |
Myo9a
myosin IXa MGI:107735 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Frontalis muscle weakness |
Dysphagia |
Difficulty walking |
Easy fatigability |
Bulbar palsy |
Fatigable weakness |
Ataxia |
EEG with polyspike wave complexes |
Choking episodes |
Intellectual disability |
Central sleep apnea |
Obstructive sleep apnea |
Areflexia |
Hyporeflexia |
Tip-toe gait |
Waddling gait |
Motor delay |
Motor polyneuropathy |
Seizure |
| Disease(s) Associated with MYO9A | |||||||||||||||||||
| congenital myasthenic syndrome |
| Mouse Phenotypes | nervous system phenotype |
seizures |
abnormal neural tube ventricular layer morphology |
small superior cervical ganglion |
reduced sympathetic cervical ganglion size |
hydrocephaly |
obstructive hydrocephaly |
enlarged third ventricle |
dilated lateral ventricle |
abnormal third ventricle morphology |
brain ventricle stenosis |
abnormal cerebral aqueduct morphology |
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| Availability | Mouse Genotype | ||||||||||||
| Myo9aem1Atuf/Myo9aem1Atuf | |||||||||||||
| Myo9atm1.2Bah/Myo9atm1.2Bah | * | ||||||||||||
| Myo9atm1b(EUCOMM)Wtsi/Myo9atm1b(EUCOMM)Wtsi | |||||||||||||
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 04/23/2024 MGI 6.23 |
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