EIF4H Back

eukaryotic translation initiation factor 4H

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NCBI Description of EIF4H

This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.

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Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


EIF4H is highly significantly mutated in
EIF4H is significantly mutated in
EIF4H is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for EIF4H