Symbol Name ID |
Eif4h
eukaryotic translation initiation factor 4H MGI:1341822 |
Darker colors indicate more annotations |
Human Phenotypes | Inguinal hernia |
Umbilical hernia |
Short stature |
Failure to thrive in infancy |
Obesity |
Intrauterine growth retardation |
Disease(s) Associated with EIF4H | ||||||
Williams-Beuren syndrome |
Mouse Phenotypes | embryonic growth retardation |
abnormal embryo size |
decreased body weight |
decreased body length |
decreased body size |
postnatal growth retardation |
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Availability | Mouse Genotype | ||||||
Eif4hGt(Ex279)Byg/Eif4hGt(Ex279)Byg | |||||||
Eif4htm1b(EUCOMM)Wtsi/Eif4htm1b(EUCOMM)Wtsi |
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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