Symbol: Name: ID: |
EIF4H eukaryotic translation initiation factor 4H GFS:2511 |
Gene name: | EIF4H |
Chromosome: | 7q11.23 |
Previous Symbols: | WBSCR1 |
Previous Names: | Williams-Beuren syndrome chromosome region 1 |
Aliases: | WSCR1, KIAA0038 |
Name Aliases: | |
Locus Type: | gene with protein product |
Mouse Genome Database ID: | MGI:1341822 | Rat Genome Database ID: | RGD:1359222 |
HGNC ID: | HGNC:12741 | RefSeq IDs: | NM_022170 |
Entrez Gene ID: | 7458 | Ensembl Gene ID: | ENSG00000106682 |
VEGA IDs: | OTTHUMG00000023025 | UniProt ID: | Q15056 |
UCSC ID: | uc003uad.1 | OMIM ID: | 603431 |
Pubmed: | PMID9516461 PMID 15078951 | ||
CCDS IDs: | CCDSCCDS5564.1 CCDS CCDS5565.1 |
Eukaryotic translation initiation factor 4H is a protein that in humans is encoded by the EIF4H gene.
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].
Function: Stimulates the RNA helicase activity of EIF4A in the translation initiation complex. Binds weakly mRNA.
Products for EIF4H gene
Catalog | Product Name | Application | Company |
GFS:E02511 | eukaryotic translation initiation factor 4H; ELISA kit | ELISA | n/a |
GFS:A02511 | eukaryotic translation initiation factor 4H; Anti | ANTIBODIES | n/a |
GFS:P02511 | eukaryotic translation initiation factor 4H; Protien | Protien | n/a |