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Description for Protein EIF4H

eukaryotic translation initiation factor 4H
1 total interacting proteins;
Icon Book Platelet Evidence (proteome studies/others : 3/2)
(platelet: 5; undefined: 1)
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] (PubMed Links)
Domains and Motifs:
  • RRM: RNA recognition motif
    • Gene Ontology:
    Gene Ontology Annotations
    KEGG - Enzyme ID(s):
    None Available
    KEGG - Orthology:
    None Available
    KEGG - Pathway(s):
    None Available
    Nomenclature / Alternative Names:
    EIF4H; WSCR1; KIAA0038; Eukaryotic translation initiation factor 4H; Williams Beuren syndrome chromosome region 1 protein; Eukaryotic translation initiation factor 4H isoform 1; Eukaryotic translation initiation factor 4H isoform 2
    Approved Symbol:
    EIF4H
    (De-) Phosphorylations:
    Total (de-) phosphorylation sites: 13
    Human (de-) phosphorylation sites: 13; No platelet phosphorylation sites
    Phosphorylation Targets:
    Total phosphorylation targets: 0
    Human phosphorylation targets: 0;Predicted platelet targets: 0
    		Protein Characteristics:
    Isoform-specific Information
    Icon DrugsAssociated Drugs (DrugBank Accession):

    None Available

    Associated Genetic Diseases:

    None Available
    		Predicted Transmembrane Domains:
  • Isoform 2 : 0
  • Isoform 1 : 0
    • Additional Identifiers:

    HPRD: 11940 Entrez Gene ID: 7458 OMIM ID: 603431 Swissprot Accession: Q15056;