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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 04/16/2024 MGI 6.23 |
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