Symbol Name ID |
Eif4h
eukaryotic translation initiation factor 4H MGI:1341822 |
Darker colors indicate more annotations |
Human Phenotypes | Malar flattening |
Clinodactyly of the 5th finger |
Hallux valgus |
Radioulnar synostosis |
Flexion contracture |
Joint hypermobility |
Down-sloping shoulders |
Pectus excavatum |
Kyphoscoliosis |
Osteopenia |
Osteoporosis |
Disease(s) Associated with EIF4H | |||||||||||
Williams-Beuren syndrome |
Mouse Phenotypes | abnormal cranium size |
decreased cranium width |
abnormal skeleton morphology |
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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) |
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last database update 09/03/2024 MGI 6.24 |
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