| Entrez gene ID | | 7458 |
| Official gene symbol | | EIF4H |
| Full name | | eukaryotic translation initiation factor 4H |
| Aliases | | ,KIAA0038,WBSCR1,WSCR1, |
| Gene summary | | 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. [provided by RefSeq] |
| Location | | Chromosome: 7 Locus: 7q11.23 |
| Gene position | | 73588706 - 73611429 Map Viewer |
| Gene orientation | | plus |
| Gene size | | 22724 bp |
| Gene sequence |
| |
| OMIM ID | | 603431 |
|