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Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)
Displaying entries 26 - 50 of 2090 in total
Pathway Name Protein Name ▼ UniProt ID Gene Symbol GlyTouCan ID
Metabolism of ingested MeSeO2H into MeSeH
  • GRIM12
  • KDRF
  • TXNRD1
Defective TPMT causes TPMT deficiency
  • TPMT
Toxicity of tetanus toxin (tetX)
  • SYB2
  • VAMP2
  • tetX
TICAM1 deficiency - HSE
  • PRVTIRB
  • TICAM1
  • TLR3
  • TRIF
Toll Like Receptor 3 (TLR3) Cascade
  • PRVTIRB
  • TICAM1
  • TLR3
  • TRIF
TRAF3 deficiency - HSE
  • CAP-1
  • CRAF1
  • PRVTIRB
  • TICAM1
  • TLR3
  • TRAF3
  • TRAFAMN
  • TRIF
TGFBR2 MSI Frameshift Mutants in Cancer
  • TGFB
  • TGFB1
  • TGFBR2
TGFBR2 Kinase Domain Mutants in Cancer
  • ALK5
  • SKR4
  • TGFB
  • TGFB1
  • TGFBR1
  • TGFBR2
Defective SLC26A2 causes chondrodysplasias
  • DTD
  • DTDST
  • SLC26A2
Metabolism of steroid hormones
  • ARSC1
  • STS
Defective CYP17A1 causes AH5
  • CYP17
  • CYP17A1
  • S17AH
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)
  • OATP2A1
  • SLC21A2
  • SLCO2A1
Defective SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR)
  • LST2
  • OATP1B3
  • OATP8
  • SLC21A8
  • SLCO1B3
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)
  • LST1
  • OATP1B1
  • OATP2
  • OATPC
  • SLC21A6
  • SLCO1B1
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)
  • OATL4
  • SLC22A12
  • URAT1
Defective SLC2A9 causes hypouricemia renal 2 (RHUC2)
  • GLUT9
  • SLC2A9
Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS)
  • GLUT2
  • SLC2A2
Defective SLC2A10 causes arterial tortuosity syndrome (ATS)
  • GLUT10
  • SLC2A10
Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1)
  • GLUT1
  • SLC2A1
Proton/oligopeptide cotransporters
  • OCTP
  • PEPT1
  • PEPT2
  • PHT1
  • PHT2
  • PTR3
  • PTR4
  • SLC15A1
  • SLC15A2
  • SLC15A3
  • SLC15A4
Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN)
  • KCC3
  • SLC12A6
Defective SLC12A3 causes Gitelman syndrome (GS)
  • NCC
  • SLC12A3
  • TSC
Defective SLC12A1 causes Bartter syndrome 1 (BS1)
  • NKCC2
  • SLC12A1
Cation-coupled Chloride cotransporters
  • KCC1
  • KCC2
  • KCC3
  • KCC4
  • KIAA1176
  • NCC
  • NKCC1
  • NKCC2
  • SLC12A1
  • SLC12A2
  • SLC12A3
  • SLC12A4
  • SLC12A5
  • SLC12A6
  • SLC12A7
  • TSC
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)
  • NCKX4
  • SLC24A4
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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 19, 2024