Supriya Ghosh (Editor)

GLUT5

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Species
  
Human

Entrez
  
6518

Human
  
Mouse

Ensembl
  
ENSG00000142583

GLUT5

Aliases
  
SLC2A5, GLUT-5, GLUT5, solute carrier family 2 member 5

External IDs
  
MGI: 1928369 HomoloGene: 74459 GeneCards: SLC2A5

GLUT5 is a fructose transporter expressed on the apical border of enterocytes in the small intestine. GLUT5 allows for fructose to be transported from the intestinal lumen into the enterocyte by facilitated diffusion due to fructose's high concentration in the intestinal lumen. GLUT5 is also expressed in skeletal muscle, testis, kidney, fat tissue (adipocytes), and brain.

Contents

Fructose malabsorption or Dietary Fructose Intolerance is a dietary disability of the small intestine, where the amount of fructose carrier in enterocytes is deficient.

In humans the GLUT5 protein is encoded by the SLC2A5 gene.

Regulation

Fructose uptake rate by GLUT5 is significantly affected by diabetes mellitus, hypertension, obesity, fructose malabsorption, and inflammation. However, age-related changes in fructose intake capability are not explained by the rate of expression of GLUT5. The absorption of fructose in the simultaneous presence of glucose is improved, while sorbitol is inhibitory.

Interactive pathway map

Click on genes, proteins and metabolites below to link to respective articles.

References

GLUT5 Wikipedia