Symbol Name ID |
Eif4h
eukaryotic translation initiation factor 4H MGI:1341822 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal arteriolar tortuosity |
Atrial septal defect |
Ventricular septal defect |
Bicuspid aortic valve |
Mitral valve prolapse |
Myxomatous mitral valve degeneration |
Peripheral pulmonary artery stenosis |
Coronary artery stenosis |
Renal artery stenosis |
Stroke |
Supravalvular aortic stenosis |
Mitral regurgitation |
Pulmonic stenosis |
Hypertension |
Portal hypertension |
Disease(s) Associated with EIF4H | |||||||||||||||
Williams-Beuren syndrome |
Mouse Phenotypes | thin ventricular wall |
hemorrhage |
|
Availability | Mouse Genotype | ||
Eif4htm1b(EUCOMM)Wtsi/Eif4htm1b(EUCOMM)Wtsi | |||
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 03/25/2025 MGI 6.24 |
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