Symbol Name ID |
Eif4h
eukaryotic translation initiation factor 4H MGI:1341822 |
Darker colors indicate more annotations |
Human Phenotypes | Retinal arteriolar tortuosity |
Malar flattening |
Full cheeks |
Midface retrusion |
Narrow forehead |
Thick lower lip vermilion |
Long philtrum |
Open mouth |
Microdontia |
Hypodontia |
Dental malocclusion |
Anteverted nares |
Broad nasal tip |
Depressed nasal bridge |
Short nose |
Medial flaring of the eyebrow |
Blepharophimosis |
Epicanthus |
Periorbital fullness |
Disease(s) Associated with EIF4H | |||||||||||||||||||
Williams-Beuren syndrome |
Mouse Phenotypes | abnormal cranium size |
decreased cranium width |
|
Availability | Mouse Genotype | ||
Eif4hGt(Ex279)Byg/Eif4hGt(Ex279)Byg |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/30/2024 MGI 6.23 |
|
|