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SLC2A2 solute carrier family 2 member 2

Gene ID: 6514, updated on 20-Apr-2024
Gene type: protein coding
Also known as: GLUT2

Summary

This gene encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in this gene are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]

Associated conditions

See all available tests in GTR for this gene

DescriptionTests
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.
GeneReviews: Not available
Fanconi-Bickel syndrome
MedGen: C3495427OMIM: 227810GeneReviews: Not available
See labs
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
GeneReviews: Not available
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.
GeneReviews: Not available
Type 2 diabetes mellitus
MedGen: C0011860OMIM: 125853GeneReviews: WFS1 Spectrum Disorder
See labs

Genomic context

Location:
3q26.2
Sequence:
Chromosome: 3; NC_000003.12 (170996347..171026720, complement)
Total number of exons:
12

Links

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