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Symbol Name ID |
Eif4h
eukaryotic translation initiation factor 4H MGI:1341822 |
| Darker colors indicate more annotations |
| Human Phenotypes | Stroke |
Cerebellar hypoplasia |
Chiari type I malformation |
Incoordination |
Poor coordination |
Vocal cord paralysis |
Attention deficit hyperactivity disorder |
Anxiety |
Atypical behavior |
Obsessive-compulsive trait |
Hyperacusis |
Phonophobia |
Short attention span |
Intellectual disability |
Sleep abnormality |
Hyperreflexia |
Gait imbalance |
Impaired visuospatial constructive cognition |
| Disease(s) Associated with EIF4H | ||||||||||||||||||
| Williams-Beuren syndrome |
| Mouse Phenotypes | decreased brain size |
enlarged lateral ventricles |
decreased corpus callosum size |
abnormal brainstem morphology |
abnormal cerebral hemisphere morphology |
small cerebellum |
abnormal dendrite morphology |
abnormal dendritic spine morphology |
decreased neuron number |
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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 07/22/2025 MGI 6.24 |
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