SLC2A7: Solute Carrier Family 2 Member 7

Glucose Transporter 7 (GLUT7) – A Facilitative Hexose Transporter with Potential Roles in Hepatic Glucose Metabolism

Gene Information Card

Symbol SLC2A7
Full Name Solute Carrier Family 2 Member 7
Gene Type Protein coding
Chromosomal Location 1p36.23
NCBI Gene ID 155184 ncbi.nlm.nih.gov/gene/155184
Ensembl ID ENSG00000197273
UniProt ID Q6P9F0
OMIM ID 610371
HGNC ID 13445
Aliases GLUT7, GLUT-7

Description

SLC2A7 (Solute Carrier Family 2 Member 7) encodes GLUT7, a facilitative glucose transporter belonging to the GLUT family. GLUT7 is a high-affinity transporter for glucose and fructose, predominantly expressed in the liver and small intestine. It is localized to the endoplasmic reticulum membrane and may play a role in hepatic glucose and fructose metabolism. The gene is located on chromosome 1p36.23 and is distinct from other GLUT isoforms in its subcellular localization and substrate specificity.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Diabetes mellitus type 2 Altered hepatic glucose transport may contribute to insulin resistance; GLUT7 expression changes observed in diabetic models Limited; expression studies in rodent models
Non-alcoholic fatty liver disease (NAFLD) Potential involvement in hepatic fructose uptake and lipogenesis Expression correlation studies
Fructose malabsorption Impaired fructose transport due to GLUT7 dysfunction Hypothetical; no direct clinical evidence

Expression Profile

Tissue Expression
Tissue nTPM level
Liver 2.3 Low
Small intestine 1.8 Low
Kidney 0.5 Not detected
Pancreas 0.3 Not detected
Skeletal muscle 0.1 Not detected
Cell Line Expression
Cell Line nTPM Notes
HepG2 1.5 Hepatocellular carcinoma cell line
Caco-2 1.2 Colorectal adenocarcinoma cell line
HEK293 0.4 Embryonic kidney cells
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.112G>A (p.Gly38Arg) Missense <0.01% Unknown; predicted to affect transporter function
c.454C>T (p.Arg152Trp) Missense <0.01% Unknown; predicted damaging by in silico tools
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in ClinVar or COSMIC.

Gain of Function (GOF)

No gain-of-function mutations described.

Dominant Negative (DN)

No dominant-negative variants identified.

Gene Ontology (GO)

• glucose transmembrane transporter activity (GO:0005355) • monosaccharide transmembrane transporter activity (GO:0015145)
• transmembrane transport (GO:0055085) • plasma membrane (GO:0005886)
• endoplasmic reticulum (GO:0005783)

Pathways

• Glucose transport (Reactome: R-HSA-189200)
• Fructose metabolism (KEGG: hsa00051)

Protein Summary

GLUT7 (UniProt Q6P9F0) is a 524-amino acid facilitative glucose/fructose transporter with 12 transmembrane domains. It shares ~68% sequence identity with GLUT5 and is localized to the endoplasmic reticulum membrane. GLUT7 has a high affinity for glucose (Km ~0.3 mM) and fructose (Km ~0.2 mM). Its expression is highest in liver and small intestine, suggesting a role in dietary sugar uptake and hepatic glucose homeostasis. No 3D structure has been solved experimentally.

Related Products

Product name Cat.No. Species Gene ID
SLC2A7 Knockout HEK293 Cell Line EDJ-KQ15277 Human 155184 Details Get a Quote
SLC2A7 Knockout HeLa Cell Line EDJ-KQ58753 Human 155184 Details Get a Quote
SLC2A7 Knockout A-549 Cell Line EDJ-KQ67238 Human 155184 Details Get a Quote
SLC2A7 Knockout HCT 116 Cell Line EDJ-KQ75635 Human 155184 Details Get a Quote
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