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Gene : EIF4H Homo sapiens

Name  ? eukaryotic translation initiation factor 4H Cytological Location  7q11.23
Brief Description  eukaryotic translation initiation factor 4H
description  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]
  • synonyms:
  • Williams-Beuren syndrome chromosome region 1,
  • HGNC:12741,
  • eIF-4H,
  • WSCR1,
  • KIAA0038,
  • WBSCR1,
  • WBSCR1,
  • NM_022170,
  • EIF4H,
  • WSCR1,
  • uc003uad.2,
  • OTTHUMG00000023025
  • identifiers:
  • 7458,
  • ENSG00000106682,
  • EIF4H

Genome feature

Region: gene ? Length: 22726  
Location: 7:74174376-74197101 Cyto location: 7q11.23


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Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

Homologue Displayer

Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

67 SN Ps

5 Cross References

15 Data Sets

10 Homologues

0 Located Features

90 Rna Seq Results