EIF4H

GENE INFORMATION

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Gene name

EIF4H (HGNC Symbol)

Synonyms

KIAA0038, WBSCR1, WSCR1

Description

eukaryotic translation initiation factor 4H (HGNC Symbol)

Entrez gene 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, Jul 2008]

Chromosome

7 (Chromosome progress)

Cytoband

q11.23

Chromosome location (bp)

73588575 - 73611431

Ensembl

ENSG00000106682 (version 73.37)

Entrez gene

7458

UniProt

Q15056 (UniProt - Evidence at protein level)

neXtProt

NX_Q15056

Antibodypedia

EIF4H antibodies
 

PROTEIN VIEW

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EIF4H-001
 
EIF4H-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

EIF4H-001 ENSP00000265753
ENST00000265753
Q15056
Show all »
Show » Show » 248 27.4 No 0
EIF4H-002 ENSP00000265754
ENST00000353999
Q15056
Show all »
Show » Show » 228 25.2 No 0