Homo sapiens (human)

Summary
Taxonomy ID
9606
PubChem Taxonomy
9606
Displaying entries 1 - 25 of 2090 in total
Pathway Name Protein Name UniProt ID Gene Symbol ▼ GlyTouCan ID
Synthesis And Processing Of GAG, GAGPOL Polyproteins
  • gag
Defective TPMT causes TPMT deficiency
  • TPMT
Defective regulation of TLR7 by endogenous ligand
  • TLR7
Toll Like Receptor 7/8 (TLR7/8) Cascade
  • TLR7
  • TLR8
TLR3 deficiency - HSE
  • TLR3
UNC93B1 deficiency - HSE
  • TLR3
  • UNC93
  • UNC93B
  • UNC93B1
Toll Like Receptor 10 (TLR10) Cascade
  • TLR10
PI Metabolism
  • TIPE3
  • TNFAIP8
  • TNFAIP8L1
  • TNFAIP8L2
  • TNFAIP8L3
Toll Like Receptor 5 (TLR5) Cascade
  • TIL3
  • TLR5
  • flaF
  • fliC
  • hag
TGFBR2 MSI Frameshift Mutants in Cancer
  • TGFB
  • TGFB1
  • TGFBR2
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
Insulin effects increased synthesis of Xylulose-5-Phosphate
  • TAL
  • TALDO
  • TALDO1
  • TALDOR
  • TKT
Toxicity of tetanus toxin (tetX)
  • SYB2
  • VAMP2
  • tetX
Toxicity of botulinum toxin type G (botG)
  • SVP65
  • SYB1
  • SYB2
  • SYT
  • SYT1
  • VAMP1
  • VAMP2
  • botG
Toxicity of botulinum toxin type C (botC)
  • SNAP
  • SNAP25
  • STX1
  • STX1A
  • STX1B
  • STX1B1
  • STX1B2
Variant SLC6A14 may confer susceptibility towards obesity
  • SLC6A14
Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ)
  • SLC39A4
  • ZIP4
Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)
  • SLC35A3
Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
  • SLC35A1
Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)
  • SLC35A1
Defective SLC34A2 causes PALM
  • SLC34A2
Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)
  • SLC34A2
Zinc efflux and compartmentalization by the SLC30 family
  • SLC30A1
  • SLC30A2
  • SLC30A3
  • SLC30A5
  • SLC30A8
  • ZNT1
  • ZNT2
  • ZNT3
  • ZNT5
  • ZNT8
  • ZNTL1
  • ZTL1
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)
  • SLC17A8
  • VGLUT3

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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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