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Symbol
Name
ID
Myo18b
myosin XVIIIb
MGI:1921626
Phenotype annotations related to muscle
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
Availability Mouse Genotype
Myo18btm1Jyo/Myo18btm1Jyo

Contributing Projects:
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
The Jackson Laboratory