Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 1826 - 1850 of 2090 in total
Pathway Name Protein Name UniProt ID Gene Symbol ▲ GlyTouCan ID
Defective GGT1 causes GLUTH
  • GGT
  • GGT1
Mtb iron assimilation by chelation
  • GIG12
  • LF
  • LTF
  • Rv2895c
  • bfr
  • bfrA
  • bfrB
  • ftn
  • irtA
  • irtB
Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane
  • GJA1
  • GJAL
Transport of connexons to the plasma membrane
  • GJB2
Signaling by NTRK3 (TRKC)
  • GLEPP1
  • NTF3
  • NTRK3
  • PTPRO
  • PTPRS
  • PTPU2
  • TRKC
GLI proteins bind promoters of Hh responsive genes to promote transcription
  • GLI
  • GLI1
  • GLI2
  • GLI3
  • THP
Activation of AMPA receptors
  • GLUA1
  • GLUH1
  • GLUR1
  • GLUR2
  • GLUR3
  • GLUR4
  • GLURC
  • GRIA1
  • GRIA2
  • GRIA3
  • GRIA4
  • GluA2
  • GluA3
  • GluA4
Activation of Na-permeable kainate receptors
  • GLUR5
  • GLUR6
  • GRIK1
  • GRIK2
Presynaptic function of Kainate receptors
  • GLUR7
  • GNB1
  • GNB2
  • GNB3
  • GNB4
  • GNB5
  • GNG10
  • GNG11
  • GNG12
  • GNG13
  • GNG2
  • GNG3
  • GNG4
  • GNG5
  • GNG7
  • GNG8
  • GNG9
  • GNGT1
  • GNGT10
  • GNGT11
  • GNGT2
  • GNGT3
  • GNGT4
  • GNGT5
  • GNGT7
  • GNGT8
  • GNGT9
  • GRIK3
  • KIAA0581
  • PLCB1
  • PLCB2
  • PLCB3
Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1)
  • GLUT1
  • SLC2A1
Defective SLC2A10 causes arterial tortuosity syndrome (ATS)
  • GLUT10
  • SLC2A10
Intestinal hexose absorption
  • GLUT2
  • GLUT5
  • NAGT
  • RSC1A1
  • SGLT1
  • SLC2A2
  • SLC2A5
  • SLC5A1
Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS)
  • GLUT2
  • SLC2A2
Defective SLC2A9 causes hypouricemia renal 2 (RHUC2)
  • GLUT9
  • SLC2A9
Sodium-coupled phosphate cotransporters
  • GLVR1
  • GLVR2
  • PIT1
  • PIT2
  • SLC20A1
  • SLC20A2
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)
  • GLVR2
  • PIT2
  • SLC20A2
Defective SLC6A5 causes hyperekplexia 3 (HKPX3)
  • GLYT2
  • NET1
  • SLC6A5
Synthesis of GDP-mannose
  • GMPPA
  • GMPPB
  • MPI
  • PMI1
  • PMM1
  • PMM2
  • PMMH22
ADP signalling through P2Y purinoceptor 12
  • GNAI1
  • GNAI2
  • GNAI2B
  • GNAI3
  • GNAT3
  • GNB1
  • GNB2
  • GNB3
  • GNB4
  • GNB5
  • GNG10
  • GNG11
  • GNG12
  • GNG13
  • GNG2
  • GNG3
  • GNG4
  • GNG5
  • GNG7
  • GNG8
  • GNG9
  • GNGT1
  • GNGT10
  • GNGT11
  • GNGT2
  • GNGT3
  • GNGT4
  • GNGT5
  • GNGT7
  • GNGT8
  • GNGT9
  • HORK3
  • P2RY12
Prostacyclin signalling through prostacyclin receptor
  • GNAS
  • GNAS1
  • GNB1
  • GNB2
  • GNB3
  • GNB4
  • GNB5
  • GNG10
  • GNG11
  • GNG12
  • GNG13
  • GNG2
  • GNG3
  • GNG4
  • GNG5
  • GNG7
  • GNG8
  • GNG9
  • GNGT1
  • GNGT10
  • GNGT11
  • GNGT2
  • GNGT3
  • GNGT4
  • GNGT5
  • GNGT7
  • GNGT8
  • GNGT9
  • GSP
  • PRIPR
  • PTGIR
G beta:gamma signalling through PLC beta
  • GNB1
  • GNB2
  • GNB3
  • GNB4
  • GNB5
  • GNG10
  • GNG11
  • GNG12
  • GNG13
  • GNG2
  • GNG3
  • GNG4
  • GNG5
  • GNG7
  • GNG8
  • GNG9
  • GNGT1
  • GNGT10
  • GNGT11
  • GNGT2
  • GNGT3
  • GNGT4
  • GNGT5
  • GNGT7
  • GNGT8
  • GNGT9
  • KIAA0581
  • PLCB1
  • PLCB2
  • PLCB3
MPS IIID - Sanfilippo syndrome D
  • GNS
Defective UGT1A1 causes hyperbilirubinemia
  • GNT1
  • UGT1
  • UGT1A1
Defective UGT1A4 causes hyperbilirubinemia
  • GNT1
  • UGT1
  • UGT1A4
Histamine receptors
  • GPCR105
  • GPCR97
  • HRH1
  • HRH2
  • HRH3
  • HRH4

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Last updated: August 19, 2024