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Tchem
EIF4H
Eukaryotic translation initiation factor 4H

Protein Summary
Description
Stimulates the RNA helicase activity of EIF4A in the translation initiation complex. Binds weakly mRNA. 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]
Uniprot Accession IDs
Gene Name
Ensembl ID
  • ENST00000265753
  • ENSP00000265753
  • ENSG00000106682
  • ENST00000353999
  • ENSP00000265754

Symbol
  • KIAA0038
  • WBSCR1
  • WSCR1
  • WSCR1
  • WBSCR1
  • eIF-4H
Illumination Graph
Knowledge Table
Most Knowledge About
Knowledge Value (0 to 1 scale)
co-expressed gene
1
virus perturbation
1
disease perturbation
0.99
interacting protein
0.99
kinase perturbation
0.99


IDG Development Level Summary
Tdark

These are targets about which virtually nothing is known. They do not have known drug or small molecule activities
- AND - satisfy two or more of the following criteria:

Pubmed score: 30.45   (req: < 5)
Gene RIFs: 13   (req: <= 3)
Antibodies: 183   (req: <= 50)
Tbio

These targets do not have known drug or small molecule activities
- AND - satisfy two or more of the following criteria:

Pubmed score: 30.45   (req: >= 5)
Gene RIFs: 13   (req: > 3)
Antibodies: 183   (req: > 50)

- OR - satisfy the following criterion:

Gene Ontology Terms: 15
Tchem

Target has at least one ChEMBL compound with an activity cutoff of < 30 nM - AND - satisfies the preceding conditions

Active Ligand: 1
Tclin

Target has at least one approved drug - AND - satisfies the preceding conditions

Active Drug: 0