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EIF4H is 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.
Gene Name: | eukaryotic translation initiation factor 4H |
Synonyms: | EIF4H, KIAA0038, WBSCR1, WSCR1, EIF-4H |
Target Sequences: | NM_022170 NP_071496.1 Q15056 |
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