Species: Hu, Mu, Rt
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
Species: Hu
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
Species: Hu
Applications: WB, IHC, IHC-P
Host: Rabbit Polyclonal
Species: Hu
Applications: WB
Species: Hu
Applications: WB
Species: Hu
Applications: AC
Species: Hu
Applications: PAGE
Species: Hu
Applications: RNAi, RNAi SP
Species: Hu
Applications: RNAi, RNAi SP
Description
eIF4H 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]
Bioinformatics
Entrez |
Human |
Uniprot |
Human Human Human Human Human Human |
Product By Gene ID |
7458 |
Alternate Names |
- WBSCR1
- KIAA0038eIF-4H
- WSCR1Williams-Beuren syndrome chromosomal region 1 protein
- Williams-Beuren syndrome chromosome region 1
- eukaryotic translation initiation factor 4H
|
PTMs for eIF4H
Learn more about PTMs related to eIF4H.
Glycosylation
Bioinformatics Tool for eIF4H
Discover related pathways, diseases and genes to eIF4H. Need help? Read the
Bioinformatics Tool Guide for instructions on using this tool.