Cellular hexose transport (Homo sapiens)

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6, 15, 17, 27, 2930, 36, 4316, 32, 35, 38, 452, 13, 2124, 33, 421, 28, 37, 41, 4411, 18, 19, 26, 313, 25, 448121214, 20, 22, 40104135, 38, 455, 7, 9, 23454, 34cytosolGlcSLC2A14 Man hexoses transportedby GLUT7/11Glc Fru GlcGlcSLC2A11 SLC2A2 SLC2A1 GlcNa+Fru SLC2A6,8,10,12Man Na+Fru, ManATPGlcSLC5As, NAGLT1miR-32SLC2A1 Glc GlcGLUT1:ATP tetramerSLC5A2Na+SLC5A9 SLC2A3 hexoses transportedby SGLT4Fru Na+Glc SLC45A3GlcGlc GlcFru SLC5A4 SLC2A7 GlcGLUT4 / SLC2A4tetramerGlcurate Glchexoses transportedby SGLT4SLC2A9Fru,Glc,urateSLC2A10 GLUT2 / SLC2A2tetramerSLC5A2 FGF21hexoses transportedby GLUT7/11NAGLT1 Fru Glc SLC2A8 ATP GlcGLUT7/11Fru,Glc,urateFru, ManMan SLC2A6 SLC2A12 SLC5A1 Glc SLC5A10GLUT1 / SLC2A1tetramerSLC2A4 ATPurate GLUT3 / SLC2A3tetramerSLC5A9GLUT14 / SLC2A14tetramerFru SLC50A1GlcMan Glc123924, 39393924, 39


Description

Two gene families are responsible for glucose transport in humans. SLC2 (encoding GLUTs) and SLC5 (encoding SGLTs) families mediate glucose absorption in the small intestine, glucose reabsorption in the kidney, glucose uptake by the brain across the blood-brain barrier and glucose release by all cells in the body. Glucose is taken up from interstitial fluid by a passive, facilitative transport driven by the diffusion gradient of glucose (and other sugars) across the plasma membrane. This process is mediated by a family of Na+-independent, facilitative glucose transporters (GLUTs) encoded by the SLC2A gene family (Zhao & Keating 2007; Wood & Trayhurn 2003). There are 14 members belonging to this family (GLUT1-12, 14 and HMIT (H+/myo-inositol symporter)). The GLUT family can be subdivided into three subclasses (I-III) based on sequence similarity and characteristic sequence motifs (Joost & Thorens 2001).

Hexoses, notably fructose, glucose, and galactose, generated in the lumen of the small intestine by breakdown of dietary carbohydrate are taken up by enterocytes lining the microvilli of the small intestine and released from them into the blood. Uptake into enterocytes is mediated by two transporters localized on the lumenal surfaces of the cells, SGLT1 (glucose and galactose, together with sodium ions) and GLUT5 (fructose). GLUT2, localized on the basolateral surfaces of enterocytes, mediates the release of these hexoses into the blood (Wright et al. 2004). GLUT2 may also play a role in hexose uptake from the gut lumen into enterocytes when the lumenal content of monosaccharides is very high (Kellet & Brot-Laroche 2005) and GLUT5 mediates fructose uptake from the blood into cells of the body, notably hepatocytes.<p>Cells take up glucose by facilitated diffusion, via glucose transporters (GLUTs) associated with the plasma membrane, a reversible reaction. Four tissue-specific GLUT isoforms are known. Glucose in the cytosol is phosphorylated by tissue-specific kinases to yield glucose 6-phosphate, which cannot cross the plasma membrane because of its negative charge. In the liver, this reaction is catalyzed by glucokinase which has a low affinity for glucose (Km about 10 mM) but is not inhibited by glucose 6-phosphate. In other tissues, this reaction is catalyzed by isoforms of hexokinase. Hexokinases are feedback-inhibited by glucose 6-phosphate and have a high affinity for glucose (Km about 0.1 mM). Liver cells can thus accumulate large amounts of glucose 6-phosphate but only when blood glucose concentrations are high, while most other tissues can take up glucose even when blood glucose concentrations are low but cannot accumulate much intracellular glucose 6-phosphate. These differences are consistent with the view that that the liver functions to buffer blood glucose concentrations, while most other tissues take up glucose to meet immediate metabolic needs.<p>Glucose 6-phosphatase, expressed in liver and kidney, allows glucose 6-phosphate generated by gluconeogenesis (both tissues) and glycogen breakdown (liver) to leave the cell. The absence of glucose 6-phosphatase from other tissues makes glucose uptake by these tissues essentially irreversible, consistent with the view that cells in these tissues take up glucose for local metabolic use.<p>Class II facilitative transporters consist of GLUT5, 7, 9 and 11 (Zhao & Keating 2007, Wood & Trayhurn 2003). View original pathway at:Reactome.</div>

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Reactome-Converter 
Pathway is converted from Reactome ID: 189200
Reactome-version 
Reactome version: 62
Reactome Author 
Reactome Author: D'Eustachio, Peter

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Bibliography

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History

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CompareRevisionActionTimeUserComment
115019view16:55, 25 January 2021ReactomeTeamReactome version 75
113464view11:54, 2 November 2020ReactomeTeamReactome version 74
112664view16:05, 9 October 2020ReactomeTeamReactome version 73
101580view11:44, 1 November 2018ReactomeTeamreactome version 66
101116view21:28, 31 October 2018ReactomeTeamreactome version 65
100644view20:02, 31 October 2018ReactomeTeamreactome version 64
100194view16:47, 31 October 2018ReactomeTeamreactome version 63
99745view15:13, 31 October 2018ReactomeTeamreactome version 62 (2nd attempt)
99310view12:46, 31 October 2018ReactomeTeamreactome version 62
97975view12:15, 28 June 2018FehrhartOntology Term : 'sugar transport pathway' added !
97974view11:48, 28 June 2018FehrhartOntology Term : 'glucose transport pathway' added !
93294view11:19, 9 August 2017ReactomeTeamNew pathway

External references

DataNodes

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NameTypeDatabase referenceComment
ATP MetaboliteCHEBI:15422 (ChEBI)
ATPMetaboliteCHEBI:15422 (ChEBI)
FGF21ProteinQ9NSA1 (Uniprot-TrEMBL)
Fru MetaboliteCHEBI:15824 (ChEBI)
Fru, ManComplexR-ALL-8876282 (Reactome)
Fru, ManComplexR-ALL-8876289 (Reactome)
Fru,Glc,urateComplexR-ALL-429078 (Reactome)
Fru,Glc,urateComplexR-ALL-429148 (Reactome)
GLUT1 / SLC2A1 tetramerComplexR-HSA-70400 (Reactome)
GLUT14 / SLC2A14 tetramerComplexR-HSA-8981567 (Reactome)
GLUT1:ATP tetramerComplexR-HSA-450089 (Reactome)
GLUT2 / SLC2A2 tetramerComplexR-HSA-70422 (Reactome)
GLUT3 / SLC2A3 tetramerComplexR-HSA-70408 (Reactome)
GLUT4 / SLC2A4 tetramerComplexR-HSA-70384 (Reactome)
GLUT7/11ComplexR-HSA-429107 (Reactome)
Glc MetaboliteCHEBI:17925 (ChEBI)
GlcMetaboliteCHEBI:17925 (ChEBI)
Man MetaboliteCHEBI:4208 (ChEBI)
NAGLT1 ProteinQ5TF39 (Uniprot-TrEMBL)
Na+MetaboliteCHEBI:29101 (ChEBI)
SLC2A1 ProteinP11166 (Uniprot-TrEMBL)
SLC2A10 ProteinO95528 (Uniprot-TrEMBL)
SLC2A11 ProteinQ9BYW1 (Uniprot-TrEMBL)
SLC2A12 ProteinQ8TD20 (Uniprot-TrEMBL)
SLC2A14 ProteinQ8TDB8 (Uniprot-TrEMBL)
SLC2A2 ProteinP11168 (Uniprot-TrEMBL)
SLC2A3 ProteinP11169 (Uniprot-TrEMBL)
SLC2A4 ProteinP14672 (Uniprot-TrEMBL)
SLC2A6 ProteinQ9UGQ3 (Uniprot-TrEMBL)
SLC2A6,8,10,12ComplexR-HSA-429047 (Reactome)
SLC2A7 ProteinQ6PXP3 (Uniprot-TrEMBL)
SLC2A8 ProteinQ9NY64 (Uniprot-TrEMBL)
SLC2A9ProteinQ9NRM0 (Uniprot-TrEMBL)
SLC45A3ProteinQ96JT2 (Uniprot-TrEMBL)
SLC50A1ProteinQ9BRV3 (Uniprot-TrEMBL)
SLC5A1 ProteinP13866 (Uniprot-TrEMBL)
SLC5A10ProteinA0PJK1 (Uniprot-TrEMBL)
SLC5A2 ProteinP31639 (Uniprot-TrEMBL)
SLC5A2ProteinP31639 (Uniprot-TrEMBL)
SLC5A4 ProteinQ9NY91 (Uniprot-TrEMBL)
SLC5A9 ProteinQ2M3M2 (Uniprot-TrEMBL)
SLC5A9ProteinQ2M3M2 (Uniprot-TrEMBL)
SLC5As, NAGLT1ComplexR-HSA-3662199 (Reactome) This CandidateSet contains sequences identified by William Pearson's analysis of Reactome catalyst entities. Catalyst entity sequences were used to identify analagous sequences that shared overall homology and active site homology. Sequences in this Candidate set were identified in an April 24, 2012 analysis.
hexoses transported by GLUT7/11ComplexR-ALL-428802 (Reactome)
hexoses transported by GLUT7/11ComplexR-ALL-428819 (Reactome)
hexoses transported by SGLT4ComplexR-ALL-429620 (Reactome)
hexoses transported by SGLT4ComplexR-ALL-429628 (Reactome)
miR-32RnaMI0000090 (miRBase mature sequence)
urate MetaboliteCHEBI:17775 (ChEBI)

Annotated Interactions

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SourceTargetTypeDatabase referenceComment
ATPArrowR-HSA-450092 (Reactome)
ATPR-HSA-450088 (Reactome)
ATPTBarR-HSA-5339524 (Reactome)
FGF21ArrowR-HSA-5339524 (Reactome)
Fru, ManArrowR-HSA-8876283 (Reactome)
Fru, ManR-HSA-8876283 (Reactome)
Fru,Glc,urateArrowR-HSA-429036 (Reactome)
Fru,Glc,urateR-HSA-429036 (Reactome)
GLUT1 / SLC2A1 tetramerArrowR-HSA-450092 (Reactome)
GLUT1 / SLC2A1 tetramerR-HSA-450088 (Reactome)
GLUT1 / SLC2A1 tetramermim-catalysisR-HSA-5339524 (Reactome)
GLUT14 / SLC2A14 tetramermim-catalysisR-HSA-8981553 (Reactome)
GLUT1:ATP tetramerArrowR-HSA-450088 (Reactome)
GLUT1:ATP tetramerR-HSA-450092 (Reactome)
GLUT2 / SLC2A2 tetramermim-catalysisR-HSA-450095 (Reactome)
GLUT2 / SLC2A2 tetramermim-catalysisR-HSA-8981574 (Reactome)
GLUT3 / SLC2A3 tetramermim-catalysisR-HSA-8981564 (Reactome)
GLUT4 / SLC2A4 tetramermim-catalysisR-HSA-8981570 (Reactome)
GLUT7/11mim-catalysisR-HSA-428779 (Reactome)
GlcArrowR-HSA-189208 (Reactome)
GlcArrowR-HSA-429094 (Reactome)
GlcArrowR-HSA-429613 (Reactome)
GlcArrowR-HSA-450095 (Reactome)
GlcArrowR-HSA-5339524 (Reactome)
GlcArrowR-HSA-8875902 (Reactome)
GlcArrowR-HSA-8876319 (Reactome)
GlcArrowR-HSA-8981553 (Reactome)
GlcArrowR-HSA-8981564 (Reactome)
GlcArrowR-HSA-8981570 (Reactome)
GlcArrowR-HSA-8981574 (Reactome)
GlcR-HSA-189208 (Reactome)
GlcR-HSA-429094 (Reactome)
GlcR-HSA-429613 (Reactome)
GlcR-HSA-450095 (Reactome)
GlcR-HSA-5339524 (Reactome)
GlcR-HSA-8875902 (Reactome)
GlcR-HSA-8876319 (Reactome)
GlcR-HSA-8981553 (Reactome)
GlcR-HSA-8981564 (Reactome)
GlcR-HSA-8981570 (Reactome)
GlcR-HSA-8981574 (Reactome)
Na+ArrowR-HSA-189208 (Reactome)
Na+ArrowR-HSA-429567 (Reactome)
Na+ArrowR-HSA-429613 (Reactome)
Na+ArrowR-HSA-8876283 (Reactome)
Na+R-HSA-189208 (Reactome)
Na+R-HSA-429567 (Reactome)
Na+R-HSA-429613 (Reactome)
Na+R-HSA-8876283 (Reactome)
R-HSA-189208 (Reactome) SLC5A2 (also known as SGLT2) in the plasma membrane co-transports extracellular sodium ions (Na+) and glucose (Glc) into the cytosol (Quick et al. 2003; Wright 2001). SLC5A2 is expressed at high levels in the kidney (Tazawa et al. 2005) and appears to be the major mediator of kidney glucose reabsorption. Human patients who lack functional SLC5A2 (e.g., Calado et al. 2004) and mouse strains lacking its homolog (Vallon et al. 2011) excrete abnormally large amounts of glucose in the urine but exhibit normal uptake of dietary glucose.
R-HSA-428779 (Reactome) SLC2A7 encodes GLUT7, a class II facilitative glucose transporter which was cloned from a human intestinal cDNA library (Li Q et al, 2004). It has a high affinity for glucose and fructose uptake. GLUT7 is found predominantly in the small intestine, colon, testis and prostate.

SLC2A11 encodes GLUT11 (Doege H et al, 2001), another member of the class II facilitative glucose transporters. It has the highest similarity with GLUT5 and in humans, three isoforms are expressed (GLUT11A-C) (Sasaki T et al, 2001). Human GLUT11 has been shown to transport glucose and fructose but not galactose when expressed in Xenopus oocytes ( Scheepers A et al, 2005).
R-HSA-429036 (Reactome) The human SLC2A9 gene encodes two isoforms of class II facilitative glucose transporter 9; GLUT9 (Phay et al. 2000) and GLUT9DeltaN (Augustin et al. 2004). GLUT9 is expressed mainly in kidney (proximal tubules of epithelial cells) and liver while GLUT9DeltaN is expressed mainly in kidney and placenta. SLC2A9 mediates the transport of urate (uric acid), the end product of purine metabolism in humans and great apes. In addition it mediates the uptake of fructose (Fru) and glucose (Glc) at a low rate (Vitart et al. 2008). Mutations in SLC2A9 influence serum urate concentrations with excess serum accumulation of urate leading to the development of gout (Vitart et al. 2008).
R-HSA-429094 (Reactome) Class III facilitative transporters consist of five members; GLUT6, 8, 10, 12 and HMIT (a H+/myo-inositol transporter). They possess a characteristic glycosylation site on loop 9 (found in loop 1 of classes I and II transporters).

Four class III facilitative transporters can transport glucose. SLC2A6 encodes GLUT6, expressed mainly in brain, spleen and leucocytes (Doege H et al, 2000a). In literature, this protein is incorrectly described as GLUT9. SLC2A8 encodes GLUT8 and is expressed in brain, testis and adipose tissue (Doege H et al, 2000b). SLC2A10 (located in the Type 2 diabetes-linked region of human chromosome 20q12-13.1) encodes GLUT10, a transporter with high affinity for glucose (McVie-Wylie AJ et al, 2001) . GLUT10 is highly expressed in liver and pancreas but is present in most tissues in lower levels. Defects in SLC2A10 are the cause of arterial tortuosity syndrome (ATS), an autosomal recessive disorder characterized by tortuosity and elongation of major arteries, often resulting in death at a young age (Coucke PJ et al, 2006). SLC2A12 encodes GLUT12, which is highly expressed in skeletal muscle, heart and prostate, with lower levels in brain, placenta and kidney. It was originally cloned from the human breast cancer cell line MCF-7 (Rogers S et al, 2002).
R-HSA-429567 (Reactome) The human gene SLC5A9 encodes a low affinity transporter for glucose and mannose (SGLT4). Of the tissues tested, SGLT4 appears to be highly expressed in the kidney and intestine, with lower levels detected in the liver. Human SGLT4 expressed in african green monkey cells exhibited glucose and mannose co-transport with Na+ ions (Tazawa S et al, 2005).
R-HSA-429613 (Reactome) The human gene SLC5A2 encodes a sodium-dependent glucose transporter, SGLT2 (Wells et al. 1992). SLC5A2 is expressed in many tissues but primarily in the kidney, specifically the renal proximal tubules (S1 and S2 segments). It is a low affinity, high capacity transporter of glucose across the apical membrane, with co-transport of Na+ ions in a 1:1 ratio. Unlike SGLT1, it doesn't transport galactose. SLC5A2 is the main transporter of glucose in the kidney, responsible for approximately 98% of glucose reabsorption (remainder by SGLT1). Defects in SLC5A2 are the cause of renal glucosuria (GLYS1), an autosomal recessive renal tubular disorder (Calado et al. 2004). A separate sodium dependent glucose transporter NAGLT1, was identified in the multifacilitator superfamily (MFS) and could be a transporter of glucose in kidney proximal tubules. Its rat orthologue, Naglt1, has been shown to mediate tubular reabsorption of glucose (Horiba et al. 2003). By similarity, SLC5A1, 4 and 9 are predicted proteins that transport glucose in a Na+-dependent manner.
R-HSA-450088 (Reactome) Cytosolic ATP reversibly associates with GLUT1. This association inhibits GLUT1 glucose transport (Blodgett et al. 2007).
R-HSA-450092 (Reactome) GLUT1:ATP complexes reversibly dissociate, restoring the glucose transport activity of GLUT1 glucose transport, with the result that depletion of cellular ATP leads to increased glucose uptake (Blodgett et al. 2007).
R-HSA-450095 (Reactome) GLUT2 (glucose transporter) homotetramers associated with the plasma membrane mediate the facilitated diffusion of glucose between the cytosol and the extracellular space, so glucose will leave cells when its intracellular concentration exceeds the extracellular one (Colville et al. 1993; Santer et al. 1997; Wu et al. 1998). In the body, such glucose export is a normal feature of liver cells when gluconeogenesis or glycogen breakdown is underway.
R-HSA-5339524 (Reactome) Tetrameric GLUT1, the SLC2A1 gene product, associated with the plasma membrane, mediates the facilitated diffusion of glucose (Glc) into cells. GLUT1 is expressed by many cell types, notably endothelial cells, red blood cells and cells of the brain. Its low Km for glucose (~1 mM) relative to normal blood glucose concentration (~5 mM) allows these cells to take up glucose independent of changes in blood glucose levels. It has been purified from red blood cells and biochemically characterized (Hruz & Mueckler 2001, Liu et al. 2001). Cytosolic ATP associates with GLUT1 and inhibits its glucose transporter activity. Fibroblast growth factor 21 (FGF21) is a potent positive regulator of glucose uptake in differentiated mouse 3T3-L1 adipocytes and in primary human adipocytes, probably acting by stimulating SLC2A1 / GLUT1 gene transcription.
R-HSA-8875902 (Reactome) Maintenance of myelin structure and function requires appropriate lipids and myelin-specific proteins, all controlled in a tight fashion. Myelin is generated by the extension of oligodendrocyte cell membranes. Damaged myelin is implicated in many demyelinating neurological disorders such as multiple sclerosis, leukodystrophies and demyelinating neuropathies. The micro-RNA miR-32 is highly expressed in the myelin-enriched regions of the brain and mature oligodendrocytes, and it promotes myelin protein expression. It can directly regulate the expression of solute carrier family 45 member 3 (SLC45A3, prostein), a prostate-specific protein expressed in normal and malignant prostate tissues (Xu et al. 2001, Kiessling et al. 2004). SLC45A3 is suggested to be a myelin-enriched putative sugar transporter and therefore, indirectly, involved in fatty acid sythesis in oligodendrocytes (Shin et al. 2012).
R-HSA-8876283 (Reactome) The sodium/glucose cotransporter 5 (SLC5A10, sodium glucose cotransporter 5, SGLT5) is a plasma membrane-bound transport protein that possesses high capacity to transport mannose (Man) and fructose (Fru) into cells (Grempler et al. 2012). SLC5A10 is exclusively expressed in the kidney and is also able to transport glucose, alpha-methyl-D-glucose (AMG) and galactose, although to a much lower extent than Man and Fru.
R-HSA-8876319 (Reactome) In mammals, glucose efflux from the liver is crucial for the maintenance of blood glucose levels (Deng & Yan 2016). Human sugar transporter SWEET1 (SLC50A1) is a ubiquitously expressed transport protein, with highest expression in oviduct, epididymis and intestine. It localises to the Golgi membrane where it may supply glucose to the Golgi for secretion from intestinal and liver cells (Chen et al. 2010).
R-HSA-8981553 (Reactome) The SLC2A14 gene appears to have arisen by duplication of the SLC2A3 gene. It is expressed only in testis. The GLUT14 / SLC2A14 protein product has not been characterized but is inferred based on sequence similarity to exist as a plasma membrane associated tetramer that mediates the facilitated diffusion of glucose (Glc) into cells (Wu & Freeze 2002).
R-HSA-8981564 (Reactome) Tetrameric GLUT3, the SLC2A3 gene product, associated with the plasma membrane, mediates the facilitated diffusion of glucose (Glc) into cells. GLUT3 is expressed by many cell types, notably in the brain. Its low Km for glucose (~1 mM) relative to normal blood glucose concentration (~5 mM) allows these cells to import glucose independent of fluctuations in blood glucose levels (Colville et al. 1993). GLUT3, like GLUT1 and 4, has a high affinity for glucose.
R-HSA-8981570 (Reactome) Tetrameric GLUT4, the SLC2A4 gene product, associated with the plasma membrane, mediates the facilitated diffusion of glucose (Glc) into cells. GLUT4 is found in heart, skeletal muscle, brain and adipose tissue. GLUT4 molecules are translocated from an intracellular store to the cell surface in response to increased insulin levels, increasing glucose transport 10-20-fold (Bryant et al. 2002; Fukumoto et al. 1989). Defects in SLC2A4 may be a cause of non-insulin-dependent diabetes mellitus (NIDDM) (Kusari et al. 1991; Choi et al. 1991).
R-HSA-8981574 (Reactome) Tetrameric GLUT2, the SLC2A2 gene product, associated with the plasma membrane, mediates the facilitated diffusion of glucose (Glc) into cells. GLUT2 is expressed on hepatocytes and pancreatic beta cells, and on the basolateral surfaces of enterocytes in the small intestine. Because of its high Km for glucose (~15-20 mM), GLUT2-mediated glucose uptake increases proportionally with increase of blood glucose concentration after a meal. This feature of the transporter is thought to enable efficient uptake of large amounts of glucose by the liver in the fed state, and to allow it to function as part of a glucose sensor coupled to insulin release in pancreatic beta cells (Thorens 2001). GLUT2 also mediates glucose export from liver cells when gluconeogenesis is underway (Colville et al. 1993; Santer et al. 1997; Wu et al. 1998). GLUT2 on enterocytes mediates the release of dietary glucose, galactose, and fructose into the circulation. This activity is annotated as part of the intestinal absorption module. Defects in SLC2A2 are the cause of Fanconi-Bickel syndrome (FBS). It is characterized by hepatorenal glycogen accumulation, proximal renal tubular dysfunction, and impaired utilization of glucose and galactose (Burwinkel et al. 1999).
SLC2A6,8,10,12mim-catalysisR-HSA-429094 (Reactome)
SLC2A9mim-catalysisR-HSA-429036 (Reactome)
SLC45A3mim-catalysisR-HSA-8875902 (Reactome)
SLC50A1mim-catalysisR-HSA-8876319 (Reactome)
SLC5A10mim-catalysisR-HSA-8876283 (Reactome)
SLC5A2mim-catalysisR-HSA-189208 (Reactome)
SLC5A9mim-catalysisR-HSA-429567 (Reactome)
SLC5As, NAGLT1mim-catalysisR-HSA-429613 (Reactome)
hexoses transported by GLUT7/11ArrowR-HSA-428779 (Reactome)
hexoses transported by GLUT7/11R-HSA-428779 (Reactome)
hexoses transported by SGLT4ArrowR-HSA-429567 (Reactome)
hexoses transported by SGLT4R-HSA-429567 (Reactome)
miR-32ArrowR-HSA-8875902 (Reactome)

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