|
Symbol Name ID |
Myo9a
myosin IXa MGI:107735 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microretrognathia |
Narrow jaw |
Congenital hip dislocation |
Arthrogryposis multiplex congenita |
Joint hypermobility |
Pectus carinatum |
Kyphoscoliosis |
Neuropathic spinal arthropathy |
Spinal rigidity |
| Disease(s) Associated with MYO9A | |||||||||
| congenital myasthenic syndrome |
| Mouse Phenotypes | fusion of vertebral arches |
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| Availability | Mouse Genotype | |
| 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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