eIF4H Products

Description

eIF4H 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]

Bioinformatics

Entrez	7458 Human
Uniprot	P49590 Human Q15056 Human NP_114381 Human NP_114381.1 Human NP_071496.1 Human NM_031992 Human
Product By Gene ID	7458
Alternate Names	WBSCR1 KIAA0038eIF-4H WSCR1Williams-Beuren syndrome chromosomal region 1 protein Williams-Beuren syndrome chromosome region 1 eukaryotic translation initiation factor 4H

Diseases related to eIF4H

Discover more about diseases related to eIF4H.

Infective Disorder
Neoplasms
Williams Syndrome
Carcinogenesis
Malignant Neoplasms
Malignant Paraganglionic Neoplasm
Growth Retardation
Learning Disorders
Neoplasm Metastasis
Malignant Tumor Of Colon
Sarcoma
Memory Disorders
Osteosarcoma
Animal Mammary Neoplasms
Patient Dependence On
Dog Diseases
Colorectal Cancer
Esophageal Neoplasms

Pathways for eIF4H

View related products by pathway and learn more about each of the pathways below.

Translation
Translational Initiation
Cell Proliferation
Cell Cycle
Associative Learning
Endocytosis
Stress Granule Assembly
Macropinocytosis
Rna Splicing

PTMs for eIF4H

Learn more about PTMs related to eIF4H.

Glycosylation

Bioinformatics Tool for eIF4H

Discover related pathways, diseases and genes to eIF4H. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.