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, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| EIF4H-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| EIF4H-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| EIF4H-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| EIF4H-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| EIF4H-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
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, Jul 2008]
Gene Symbol : EIF4H
Gene Name : Eukaryotic translation initiation factor 4H
Chromosome : CHR 7: 741,743,75-741,971,00
Locus : 7q11.23
Alt. Genes : HIPK3
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.