Symbol Name ID |
Eif4h
eukaryotic translation initiation factor 4H MGI:1341822 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal arteriolar tortuosity |
Blue irides |
Hypotelorism |
Strabismus |
Abnormality of refraction |
Amblyopia |
Disease(s) Associated with EIF4H | ||||||
Williams-Beuren syndrome |
Mouse Phenotypes | abnormal retina inner nuclear layer morphology |
abnormal retina outer nuclear layer morphology |
decreased total retina thickness |
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Availability | Mouse Genotype | |||
Eif4htm1b(EUCOMM)Wtsi/Eif4h+ |
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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