GlyCosmos Pathways

Integrated of pathway data, containing glycoproteins and glycans obtained from Reactome and the Metabolism of carbohydrates in Escherichia coli O-antigens obtained from ECODAB. Search by pathway name, species, and protein name.

Source Last Updated
Reactome November 12, 2024
ECODAB April 1, 2019
Displaying entries 51 - 75 of 2074 in total
Pathway Name Protein Name ▼ UniProt ID Gene Symbol Organism GlyTouCan ID
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)
  • GLVR2
  • PIT2
  • SLC20A2
Homo sapiens (human)
Sodium-coupled phosphate cotransporters
  • GLVR1
  • GLVR2
  • PIT1
  • PIT2
  • SLC20A1
  • SLC20A2
Homo sapiens (human)
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)
  • NPT2C
  • NPTIIC
  • SLC34A3
Homo sapiens (human)
Defective SLC34A2 causes PALM
  • SLC34A2
Homo sapiens (human)
Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)
  • SLC34A2
Homo sapiens (human)
Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)
  • NPT2
  • SLC17A2
  • SLC34A1
Homo sapiens (human)
Type II Na+/Pi cotransporters
  • NPT2
  • NPT2C
  • NPTIIC
  • SLC17A2
  • SLC34A1
  • SLC34A2
  • SLC34A3
Homo sapiens (human)
Defective SLC6A2 causes orthostatic intolerance (OI)
  • NAT1
  • NET1
  • SLC6A2
  • SLC6A5
Homo sapiens (human)
Defective SLC6A19 causes Hartnup disorder (HND)
  • B0AT1
  • SLC6A19
Homo sapiens (human)
Defective SLC6A19 causes Hartnup disorder (HND)
  • B0AT1
  • SLC6A19
Homo sapiens (human)
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
  • DAT1
  • SLC6A3
Homo sapiens (human)
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)
  • DAT1
  • SLC6A3
Homo sapiens (human)
Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
  • SIT1
  • SLC6A20
  • XT3
  • XTRP3
Homo sapiens (human)
Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)
  • SIT1
  • SLC6A20
  • XT3
  • XTRP3
Homo sapiens (human)
Variant SLC6A14 may confer susceptibility towards obesity
  • SLC6A14
Homo sapiens (human)
Defective SLC6A5 causes hyperekplexia 3 (HKPX3)
  • GLYT2
  • NET1
  • SLC6A5
Homo sapiens (human)
Reuptake of GABA
  • BGT1
  • GABATR
  • GABT1
  • GABT3
  • GAT1
  • GAT2
  • GAT3
  • SLC6A1
  • SLC6A11
  • SLC6A12
  • SLC6A13
Homo sapiens (human)
Defective SLC17A5 causes Salla disease (SD) and ISSD
  • SLC17A5
Homo sapiens (human)
Defective visual phototransduction due to OPN1SW loss of function
  • BCP
  • OPN1SW
Homo sapiens (human)
Integration of energy metabolism
  • PPP2CA
  • PPP2CB
  • PPP2R1A
  • PPP2R1B
  • PPP2R5D
Homo sapiens (human)
STAT6-mediated induction of chemokines
  • ERIS
  • MITA
  • NAK
  • STAT6
  • STING
  • STING1
  • TBK1
  • TMEM173
Homo sapiens (human)
SUMO is proteolytically processed
  • KIAA1331
  • SENP1
  • SENP2
  • SENP5
  • SMT3A
  • SMT3B
  • SMT3C
  • SMT3H1
  • SMT3H2
  • SMT3H3
  • SUMO1
  • SUMO2
  • SUMO3
  • UBL1
Homo sapiens (human)
SUMO is conjugated to E1 (UBA2:SAE1)
  • AOS1
  • SAE1
  • SAE2
  • SMT3A
  • SMT3B
  • SMT3C
  • SMT3H1
  • SMT3H2
  • SMT3H3
  • SUA1
  • SUMO1
  • SUMO2
  • SUMO3
  • UBA2
  • UBL1
  • UBLE1A
  • UBLE1B
Homo sapiens (human)
Synthesis of wybutosine at G37 of tRNA(Phe)
  • C1orf171
  • C2orf60
  • KIAA0547
  • KIAA1393
  • LCMT2
  • RSAFD1
  • TRM12
  • TRM5
  • TRMT12
  • TRMT5
  • TYW1
  • TYW2
  • TYW3
  • TYW4
  • TYW5
Homo sapiens (human)
SLIT2:ROBO1 increases RHOA activity
  • ARH12
  • ARHA
  • DUTT1
  • MYO9B
  • MYR5
  • RHO12
  • RHOA
  • ROBO1
  • SLIL3
  • SLIT2
Homo sapiens (human)

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Last updated: December 9, 2024