MGP Database

New search | Record Overview | Ontology/Pathway Information | Domain Information | UniProt Annotations | Related Proteins
MGP002852

Ontology/Pathway Information

Entrez Gene ID6513
Gene Namesolute carrier family 2 (facilitated glucose transporter), member 1
Gene Symbol SLC2A1
SpeciesHomo sapiens
Gene Ontology (GO Annotations)
GO IDSourceTypeDescription
GO:0016323 IEA:EnsemblCbasolateral plasma membrane
GO:0072562 IDA:UniProtKBCblood microparticle
GO:0005901 IEA:EnsemblCcaveola
GO:0005911 IEA:EnsemblCcell-cell junction
GO:0030864 IDA:UniProtKBCcortical actin cytoskeleton
GO:0070062 IDA:UniProtKBCextracellular vesicular exosome
GO:0001939 IEA:EnsemblCfemale pronucleus
GO:0005887 IDA:UniProtKBCintegral component of plasma membrane
GO:0042470 IEA:UniProtKB-SubCellCmelanosome
GO:0016020 TAS:ProtIncCmembrane
GO:0030496 IDA:UniProtKBCmidbody
GO:0005886 IDA:HPACplasma membrane
GO:0033300 IEA:EnsemblFdehydroascorbic acid transporter activity
GO:0055056 IEA:EnsemblFD-glucose transmembrane transporter activity
GO:0005355 IDA:UniProtKBFglucose transmembrane transporter activity
GO:0042802 IPI:IntActFidentical protein binding
GO:0043621 IDA:UniProtKBFprotein self-association
GO:0042910 IEA:EnsemblFxenobiotic transporter activity
GO:0005975 TAS:ReactomePcarbohydrate metabolic process
GO:0042149 IEA:EnsemblPcellular response to glucose starvation
GO:0006112 TAS:ReactomePenergy reserve metabolic process
GO:0015758 IDA:UniProtKBPglucose transport
GO:0008645 TAS:ReactomePhexose transport
GO:0019852 TAS:ReactomePL-ascorbic acid metabolic process
GO:0006461 IDA:UniProtKBPprotein complex assembly
GO:0050796 TAS:ReactomePregulation of insulin secretion
GO:0006970 IEA:EnsemblPresponse to osmotic stress
GO:0044281 TAS:ReactomePsmall molecule metabolic process
GO:0055085 TAS:ReactomePtransmembrane transport
GO:0006766 TAS:ReactomePvitamin metabolic process
GO:0006767 TAS:ReactomePwater-soluble vitamin metabolic process
REACTOME Pathway Links
REACTOME Pathway IDDescription
REACT_169280Defective AMN causes hereditary megaloblastic anemia 1
REACT_169403Defective BTD causes biotidinase deficiency
REACT_169178Defective CD320 causes methylmalonic aciduria
REACT_169132Defective CUBN causes hereditary megaloblastic anemia 1
REACT_169415Defective GIF causes intrinsic factor deficiency
REACT_169312Defective HLCS causes multiple carboxylase deficiency
REACT_169363Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
REACT_169316Defective MMAA causes methylmalonic aciduria type cblA
REACT_169318Defective MMAB causes methylmalonic aciduria type cblB
REACT_169169Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
REACT_169256Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
REACT_169149Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
REACT_169439Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
REACT_169313Defective MUT causes methylmalonic aciduria mut type
REACT_169120Defective TCN2 causes hereditary megaloblastic anemia
REACT_169238Defects in biotin (Btn) metabolism
REACT_169429Defects in cobalamin (B12) metabolism
REACT_169385Defects in vitamin and cofactor metabolism
REACT_116125Disease
REACT_212Glucose transport
REACT_264090Glycogen storage diseases
REACT_9441Hexose transport
REACT_1505Integration of energy metabolism
REACT_111217Metabolism
REACT_474Metabolism of carbohydrates
REACT_11193Metabolism of vitamins and cofactors
REACT_11238Metabolism of water-soluble vitamins and cofactors
REACT_264430Myoclonic epilepsy of Lafora
REACT_18325Regulation of insulin secretion
REACT_19118SLC-mediated transmembrane transport
REACT_15518Transmembrane transport of small molecules
REACT_11202Vitamin C (ascorbate) metabolism
SMP Pathway Links
SMP IDDescription
SMP00579Congenital disorder of glycosylation CDG-IId
SMP00580GLUT-1 deficiency syndrome
SMP00444Lactose Synthesis
  logo