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 **301 - 325** of **2090** in total

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Pathway Name	Protein Name	UniProt ID ▼	Gene Symbol	Organism
Interleukin-21 signaling	Cytokine receptor common subunit gamma Interleukin-21 receptor Interleukin-21 Signal transducer and activator of transcription 1-alpha/beta Signal transducer and activator of transcription 3 Signal transducer and activator of transcription 4 Signal transducer and activator of transcription 5A Signal transducer and activator of transcription 5B Tyrosine-protein kinase JAK1 Tyrosine-protein kinase JAK3	P23458 P31785 P40763 P42224 P42229 P51692 P52333 Q14765 Q9HBE4 Q9HBE5	APRF IL21 IL21R IL2RG JAK1 JAK1A JAK1B JAK3 NILR STAT1 STAT3 STAT4 STAT5 STAT5A STAT5B	Homo sapiens (human)
COX reactions	Prostaglandin G/H synthase 1	P23219	COX1 PTGS1	Homo sapiens (human)
Signaling by FGFR3 fusions in cancer	Fibroblast growth factor receptor 3	P22607	FGFR3 JTK4	Homo sapiens (human)
t(4;14) translocations of FGFR3	Fibroblast growth factor receptor 3	P22607	FGFR3 JTK4	Homo sapiens (human)
FGFR4 mutant receptor activation	Fibroblast growth factor receptor 4	P22455	FGFR4 JTK2 TKF	Homo sapiens (human)
Defective UGT1A4 causes hyperbilirubinemia	UDP-glucuronosyltransferase 1A4	P22310	GNT1 UGT1 UGT1A4	Homo sapiens (human)
Defective UGT1A1 causes hyperbilirubinemia	UDP-glucuronosyltransferase 1A1	P22309	GNT1 UGT1 UGT1A1	Homo sapiens (human)
MPS II - Hunter syndrome	Iduronate 2-sulfatase	P22304	IDS SIDS	Homo sapiens (human)
Defective MMAA causes MMA, cblA type	Methylmalonic aciduria type A protein, mitochondrial Methylmalonyl-CoA mutase, mitochondrial	P22033 Q8IVH4	MMAA MMUT MUT	Homo sapiens (human)
Defective MUT causes MMAM	Methylmalonic aciduria type A protein, mitochondrial Methylmalonyl-CoA mutase, mitochondrial	P22033 Q8IVH4	MMAA MMUT MUT	Homo sapiens (human)
Cobalamin (Cbl) metabolism	Cobalamin trafficking protein CblD Corrinoid adenosyltransferase MMAB Cyanocobalamin reductase / alkylcobalamin dealkylase Methionine synthase reductase Methionine synthase Methylmalonic aciduria type A protein, mitochondrial Methylmalonyl-CoA mutase, mitochondrial	P22033 Q8IVH4 Q96EY8 Q99707 Q9H3L0 Q9UBK8 Q9Y4U1	C2orf25 CL25022 MMAA MMAB MMACHC MMADHC MMUT MTR MTRR MUT	Homo sapiens (human)
Signaling by FGFR2 amplification mutants	Fibroblast growth factor receptor 2	P21802	BEK FGFR2 KGFR KSAM	Homo sapiens (human)
Signaling by FGFR2 fusions	Fibroblast growth factor receptor 2	P21802	BEK FGFR2 KGFR KSAM	Homo sapiens (human)
Prostanoid ligand receptors	Prostacyclin receptor Prostaglandin D2 receptor 2 Prostaglandin D2 receptor Prostaglandin E2 receptor EP1 subtype Prostaglandin E2 receptor EP2 subtype Prostaglandin E2 receptor EP3 subtype Prostaglandin E2 receptor EP4 subtype Prostaglandin F2-alpha receptor Thromboxane A2 receptor	P21731 P34995 P35408 P43088 P43115 P43116 P43119 Q13258 Q9Y5Y4	CRTH2 DL1R GPR44 PRIPR PTGDR PTGDR2 PTGER1 PTGER2 PTGER3 PTGER4 PTGFR PTGIR TBXA2R	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)
Defective ABCB4 causes PFIC3, ICP3 and GBD1	Phosphatidylcholine translocator ABCB4	P21439	ABCB4 MDR3 PGY3	Homo sapiens (human)
Defective MAOA causes BRUNS	Amine oxidase [flavin-containing] A	P21397	MAOA	Homo sapiens (human)
Clearance of dopamine	Amine oxidase [flavin-containing] A Sodium-dependent dopamine transporter	P21397 Q01959	DAT1 MAOA SLC6A3	Homo sapiens (human)
Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB	Amine oxidase [flavin-containing] A Amine oxidase [flavin-containing] B	P21397 P27338	MAOA MAOB	Homo sapiens (human)
Enzymatic degradation of Dopamine by monoamine oxidase	Amine oxidase [flavin-containing] A Catechol O-methyltransferase	P21397 P21964	COMT MAOA	Homo sapiens (human)
Enzymatic degradation of dopamine by COMT	Amine oxidase [flavin-containing] A Catechol O-methyltransferase Transmembrane O-methyltransferase	P21397 P21964 Q8WZ04	COMT COMT2 LRTOMT MAOA TOMT	Homo sapiens (human)
Cell-extracellular matrix interactions	Alpha-parvin Beta-parvin Fermitin family homolog 2 Filamin-A Filamin-C Filamin-binding LIM protein 1 Integrin-linked protein kinase LIM and senescent cell antigen-like-containing domain protein 1 LIM and senescent cell antigen-like-containing domain protein 2 Vasodilator-stimulated phosphoprotein	P21333 P48059 P50552 Q13418 Q14315 Q7Z4I7 Q8WUP2 Q96AC1 Q9HBI1 Q9NVD7	ABPL FBLIM1 FBLP1 FERMT2 FLN FLN1 FLN2 FLNA FLNC ILK ILK1 ILK2 KIND2 LIMS1 LIMS2 MIG2 MXRA2 PARVA PARVB PINCH PINCH1 PINCH2 PLEKHC1 VASP	Homo sapiens (human)
MTF1 activates gene expression	Beta-synuclein Cysteine and glycine-rich protein 1 Metal regulatory transcription factor 1	P21291 Q14872 Q16143	CSRP CSRP1 CYRP MTF1 SNCB	Homo sapiens (human)
MDK and PTN in ALK signaling	ALK tyrosine kinase receptor Midkine Pleiotrophin Receptor-type tyrosine-protein phosphatase zeta	P21246 P21741 P23471 Q9UM73	ALK HBNF1 HTPZP2 MDK MK1 NEGF1 NEGF2 PTN PTPRZ PTPRZ1 PTPRZ2 PTPZ	Homo sapiens (human)
NTF3 activates NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Neurotrophin-3	P20783 Q16620	NTF3 NTRK2 TRKB	Homo sapiens (human)

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