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SLC2A2

Function

Facilitative hexose transporter that mediates the transport of glucose, fructose and galactose (PubMed:16186102, PubMed:23396969, PubMed:28083649, PubMed:8027028, PubMed:8457197). Likely mediates the bidirectional transfer of glucose across the plasma membrane of hepatocytes and is responsible for uptake of glucose by the beta cells; may comprise part of the glucose-sensing mechanism of the beta cell (PubMed:8027028). May also participate with the Na(+)/glucose cotransporter in the transcellular transport of glucose in the small intestine and kidney (PubMed:3399500). Also able to mediate the transport of dehydroascorbate (PubMed:23396969).

Involvement in disease

Fanconi-Bickel syndrome

FBS

Rare, well-defined clinical entity, inherited in an autosomal recessive mode and characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, and impaired utilization of glucose and galactose.

None

The disease is caused by variants affecting the gene represented in this entry.

Post-translational modifications

N-glycosylated; required for stability and retention at the cell surface of pancreatic beta cells.

Sequence Similarities

Belongs to the major facilitator superfamily. Sugar transporter (TC 2.A.1.1) family. Glucose transporter subfamily.

Tissue Specificity

Liver, insulin-producing beta cell, small intestine and kidney.

Cellular localization

Alternative names

GLUT2, SLC2A2, GLUT-2

swissprot:P11168 entrezGene:6514 omim:138160