Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 2051 - 2075 of 2090 in total
Pathway Name Protein Name ▲ UniProt ID Gene Symbol GlyTouCan ID
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)
  • OATP2A1
  • SLC21A2
  • SLCO2A1
Defective CYP17A1 causes AH5
  • CYP17
  • CYP17A1
  • S17AH
Metabolism of steroid hormones
  • ARSC1
  • STS
Defective SLC26A2 causes chondrodysplasias
  • DTD
  • DTDST
  • SLC26A2
TGFBR2 Kinase Domain Mutants in Cancer
  • ALK5
  • SKR4
  • TGFB
  • TGFB1
  • TGFBR1
  • TGFBR2
TGFBR2 MSI Frameshift Mutants in Cancer
  • TGFB
  • TGFB1
  • TGFBR2
TRAF3 deficiency - HSE
  • CAP-1
  • CRAF1
  • PRVTIRB
  • TICAM1
  • TLR3
  • TRAF3
  • TRAFAMN
  • TRIF
TICAM1 deficiency - HSE
  • PRVTIRB
  • TICAM1
  • TLR3
  • TRIF
Toll Like Receptor 3 (TLR3) Cascade
  • PRVTIRB
  • TICAM1
  • TLR3
  • TRIF
Toxicity of tetanus toxin (tetX)
  • SYB2
  • VAMP2
  • tetX
Defective TPMT causes TPMT deficiency
  • TPMT
Metabolism of ingested MeSeO2H into MeSeH
  • GRIM12
  • KDRF
  • TXNRD1
Defective TBXAS1 causes GHDD
  • CYP5
  • CYP5A1
  • TBXAS1
  • TXAS
Toll Like Receptor 10 (TLR10) Cascade
  • TLR10
TLR3 deficiency - HSE
  • TLR3
Toll Like Receptor 7/8 (TLR7/8) Cascade
  • TLR7
  • TLR8
Defective regulation of TLR7 by endogenous ligand
  • TLR7
Insulin effects increased synthesis of Xylulose-5-Phosphate
  • TAL
  • TALDO
  • TALDO1
  • TALDOR
  • TKT
TALDO1 deficiency: failed conversion of SH7P, GA3P to Fru(6)P, E4P
  • TAL
  • TALDO
  • TALDO1
  • TALDOR
TALDO1 deficiency: failed conversion of Fru(6)P, E4P to SH7P, GA3P
  • TAL
  • TALDO
  • TALDO1
  • TALDOR
GLI proteins bind promoters of Hh responsive genes to promote transcription
  • GLI
  • GLI1
  • GLI2
  • GLI3
  • THP
Beta oxidation of palmitoyl-CoA to myristoyl-CoA
  • ACADVL
  • HADH
  • HADHA
  • HADHB
  • VLCAD
PI Metabolism
  • TIPE3
  • TNFAIP8
  • TNFAIP8L1
  • TNFAIP8L2
  • TNFAIP8L3
Defective ALG14 causes ALG14-CMS
  • ALG13
  • ALG14
  • CXorf45
  • GLT28D1
Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)
  • SLC35A3

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