Symbol Name ID |
Myo18b
myosin XVIIIb MGI:1921626 |
Darker colors indicate more annotations |
Human Phenotypes | Flexion contracture |
Generalized hypotonia |
Nemaline bodies |
Myopathy |
Disease(s) Associated with MYO18B | ||||
Klippel-Feil syndrome 4 |
Mouse Phenotypes | abnormal myocardium layer morphology |
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Availability | Mouse Genotype | |
Myo18btm1Jyo/Myo18btm1Jyo |
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 03/19/2024 MGI 6.23 |
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