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TBC1D4 TBC1 domain family member 4

Gene ID: 9882, updated on 13-Nov-2024
Gene type: protein coding
Also known as: AS160; NIDDM5

Summary

This gene is a member of the Tre-2/BUB2/CDC16 domain family. The protein encoded by this gene is a Rab-GTPase-activating protein, and contains two phopshotyrosine-binding domains (PTB1 and PTB2), a calmodulin-binding domain (CBD), a Rab-GTPase domain, and multiple AKT phosphomotifs. This protein is thought to play an important role in glucose homeostasis by regulating the insulin-dependent trafficking of the glucose transporter 4 (GLUT4), important for removing glucose from the bloodstream into skeletal muscle and fat tissues. Reduced expression of this gene results in an increase in GLUT4 levels at the plasma membrane, suggesting that this protein is important in intracellular retention of GLUT4 under basal conditions. When exposed to insulin, this protein is phosphorylated, dissociates from GLUT4 vesicles, resulting in increased GLUT4 at the cell surface, and enhanced glucose transport. Phosphorylation of this protein by AKT is required for proper translocation of GLUT4 to the cell surface. Individuals homozygous for a mutation in this gene are at higher risk for type 2 diabetes and have higher levels of circulating glucose and insulin levels after glucose ingestion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
GeneReviews: Not available
Diabetes mellitus, noninsulin-dependent, 5
MedGen: C4015183OMIM: 616087GeneReviews: Not available
not available
Genome-wide association study in a Chinese population with diabetic retinopathy.
GeneReviews: Not available

Genomic context

Location:
13q22.2
Sequence:
Chromosome: 13; NC_000013.11 (75283503..75482169, complement)
Total number of exons:
23

Links

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