GlyCosmos Portal

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	March 20, 2024
ECODAB	April 1, 2019

Displaying entries **1 - 25** of **2090** in total

1

2

3

4

5

…

Next ›

Last »
Pathway Name	Protein Name	UniProt ID	Gene Symbol ▼	Organism
Synthesis And Processing Of GAG, GAGPOL Polyproteins	Gag polyprotein	P04591	gag	Homo sapiens (human)
Defective TPMT causes TPMT deficiency	Thiopurine S-methyltransferase	P51580	TPMT	Homo sapiens (human)
Defective regulation of TLR7 by endogenous ligand	Toll-like receptor 7	Q9NYK1	TLR7	Homo sapiens (human)
Toll Like Receptor 7/8 (TLR7/8) Cascade	Toll-like receptor 7 Toll-like receptor 8	Q9NR97 Q9NYK1	TLR7 TLR8	Homo sapiens (human)
TLR3 deficiency - HSE	Toll-like receptor 3	O15455	TLR3	Homo sapiens (human)
UNC93B1 deficiency - HSE	Protein unc-93 homolog B1 Toll-like receptor 3	O15455 Q9H1C4	TLR3 UNC93 UNC93B UNC93B1	Homo sapiens (human)
Toll Like Receptor 10 (TLR10) Cascade	Toll-like receptor 10	Q9BXR5	TLR10	Homo sapiens (human)
PI Metabolism	Tumor necrosis factor alpha-induced protein 8-like protein 1 Tumor necrosis factor alpha-induced protein 8-like protein 2 Tumor necrosis factor alpha-induced protein 8-like protein 3 Tumor necrosis factor alpha-induced protein 8	O95379 Q5GJ75 Q6P589 Q8WVP5	TIPE3 TNFAIP8 TNFAIP8L1 TNFAIP8L2 TNFAIP8L3	Homo sapiens (human)
Toll Like Receptor 5 (TLR5) Cascade	Flagellin Toll-like receptor 5	O60602 P04949	TIL3 TLR5 flaF fliC hag	Homo sapiens (human)
TGFBR2 MSI Frameshift Mutants in Cancer	TGF-beta receptor type-2 Transforming growth factor beta-1 proprotein	P01137 P37173	TGFB TGFB1 TGFBR2	Homo sapiens (human)
TALDO1 deficiency: failed conversion of SH7P, GA3P to Fru(6)P, E4P	Transaldolase	P37837	TAL TALDO TALDO1 TALDOR	Homo sapiens (human)
TALDO1 deficiency: failed conversion of Fru(6)P, E4P to SH7P, GA3P	Transaldolase	P37837	TAL TALDO TALDO1 TALDOR	Homo sapiens (human)
Insulin effects increased synthesis of Xylulose-5-Phosphate	Transaldolase Transketolase	P29401 P37837	TAL TALDO TALDO1 TALDOR TKT	Homo sapiens (human)
Toxicity of tetanus toxin (tetX)	Tetanus toxin Vesicle-associated membrane protein 2	P04958 P63027	SYB2 VAMP2 tetX	Homo sapiens (human)
Toxicity of botulinum toxin type G (botG)	Botulinum neurotoxin type G Synaptotagmin-1 Vesicle-associated membrane protein 1 Vesicle-associated membrane protein 2	P21579 P23763 P63027 Q60393	SVP65 SYB1 SYB2 SYT SYT1 VAMP1 VAMP2 botG	Homo sapiens (human)
Toxicity of botulinum toxin type C (botC)	Botulinum neurotoxin type C Synaptosomal-associated protein 25 Syntaxin-1A Syntaxin-1B	P18640 P60880 P61266 Q16623	SNAP SNAP25 STX1 STX1A STX1B STX1B1 STX1B2	Homo sapiens (human)
Variant SLC6A14 may confer susceptibility towards obesity	Sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)	Q9UN76	SLC6A14	Homo sapiens (human)
Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ)	Zinc transporter ZIP4	Q6P5W5	SLC39A4 ZIP4	Homo sapiens (human)
Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)	UDP-N-acetylglucosamine transporter	Q9Y2D2	SLC35A3	Homo sapiens (human)
Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)	CMP-sialic acid transporter	P78382	SLC35A1	Homo sapiens (human)
Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)	CMP-sialic acid transporter	P78382	SLC35A1	Homo sapiens (human)
Defective SLC34A2 causes PALM	Sodium-dependent phosphate transport protein 2B	O95436	SLC34A2	Homo sapiens (human)
Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)	Sodium-dependent phosphate transport protein 2B	O95436	SLC34A2	Homo sapiens (human)
Zinc efflux and compartmentalization by the SLC30 family	Probable proton-coupled zinc antiporter SLC30A3 Proton-coupled zinc antiporter SLC30A1 Proton-coupled zinc antiporter SLC30A2 Proton-coupled zinc antiporter SLC30A5 Proton-coupled zinc antiporter SLC30A8	Q8IWU4 Q8TAD4 Q99726 Q9BRI3 Q9Y6M5	SLC30A1 SLC30A2 SLC30A3 SLC30A5 SLC30A8 ZNT1 ZNT2 ZNT3 ZNT5 ZNT8 ZNTL1 ZTL1	Homo sapiens (human)
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)	Vesicular glutamate transporter 3	Q8NDX2	SLC17A8 VGLUT3	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements