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 **2001 - 2025** of **2090** in total

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Pathway Name	Protein Name	UniProt ID	Gene Symbol ▲	Organism	GlyTouCan ID
MyD88 deficiency (TLR5)	Flagellin Myeloid differentiation primary response protein MyD88 Toll-like receptor 5	O60602 P04949 Q99836	MYD88 TIL3 TLR5 flaF fliC hag	Homo sapiens (human)
Sodium-coupled sulphate, di- and tri-carboxylate transporters	Na(+)/citrate cotransporter Na(+)/dicarboxylate cotransporter 3 Solute carrier family 13 member 1 Solute carrier family 13 member 2 Solute carrier family 13 member 4	Q13183 Q86YT5 Q8WWT9 Q9BZW2 Q9UKG4	NACT NADC1 NADC3 NAS1 NASI1 SDCT1 SDCT2 SLC13A1 SLC13A2 SLC13A3 SLC13A4 SLC13A5 SUT1	Homo sapiens (human)
MPS IIIB - Sanfilippo syndrome B	Alpha-N-acetylglucosaminidase	P54802	NAGLU UFHSD1	Homo sapiens (human)
Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM)	Sodium/glucose cotransporter 1	P13866	NAGT SGLT1 SLC5A1	Homo sapiens (human)	G58161NS
POU5F1 (OCT4), SOX2, NANOG repress genes related to differentiation	Homeobox protein NANOG POU domain, class 5, transcription factor 1 Transcription factor SOX-2	P48431 Q01860 Q9H9S0	NANOG OCT3 OCT4 OTF3 POU5F1 SOX2	Homo sapiens (human)
Defective SLC6A2 causes orthostatic intolerance (OI)	Sodium-dependent noradrenaline transporter	P23975	NAT1 NET1 SLC6A2 SLC6A5	Homo sapiens (human)
Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA)	Electrogenic sodium bicarbonate cotransporter 1	Q9Y6R1	NBC NBC1 NBCE1 SLC4A4	Homo sapiens (human)
Defective SLC12A3 causes Gitelman syndrome (GS)	Solute carrier family 12 member 3	P55017	NCC SLC12A3 TSC	Homo sapiens (human)
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)	Sodium/potassium/calcium exchanger 4	Q8NFF2	NCKX4 SLC24A4	Homo sapiens (human)
Peptide hormone biosynthesis	Neuroendocrine convertase 1 Pro-opiomelanocortin	P01189 P29120	NEC1 PCSK1 POMC	Homo sapiens (human)
NEIL3-mediated resolution of ICLs	Endonuclease 8-like 3	Q8TAT5	NEIL3	Homo sapiens (human)
Defective Base Excision Repair Associated with NEIL3	Endonuclease 8-like 3	Q8TAT5	NEIL3	Homo sapiens (human)
Ceramide signalling	Beta-nerve growth factor Sphingomyelin phosphodiesterase 2 Tumor necrosis factor receptor superfamily member 16	O60906 P01138 P08138	NGF NGFB NGFR SMPD2 TNFRSF16	Homo sapiens (human)
NFG and proNGF binds to p75NTR	Beta-nerve growth factor Sortilin-related VPS10 domain containing receptor 3 Tumor necrosis factor receptor superfamily member 16	P01138 P08138 Q17R88	NGF NGFB NGFR SORCS3 TNFRSF16	Homo sapiens (human)
Defective SLC9A9 causes autism 16 (AUTS16)	Sodium/hydrogen exchanger 9	Q8IVB4	NHE9 SLC9A9	Homo sapiens (human)
Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)	Sodium/iodide cotransporter	Q92911	NIS SLC5A5	Homo sapiens (human)
Tachykinin receptors bind tachykinins	Neuromedin-K receptor Protachykinin-1 Substance-K receptor Substance-P receptor Tachykinin-3	P20366 P21452 P25103 P29371 Q9UHF0	NK1R NK2R NK3R NKA NKNA NKNAR NKNB TAC1 TAC1R TAC2 TAC2R TAC3 TAC3R TACR1 TACR2 TACR3	Homo sapiens (human)
Defective SLC12A1 causes Bartter syndrome 1 (BS1)	Solute carrier family 12 member 1	Q13621	NKCC2 SLC12A1	Homo sapiens (human)
Organic anion transport	Organic anion transporter 3 Solute carrier family 22 member 11 Solute carrier family 22 member 12 Solute carrier family 22 member 6 Solute carrier family 22 member 7	Q4U2R8 Q8TCC7 Q96S37 Q9NSA0 Q9Y694	NLT OAT1 OAT2 OAT3 OAT4 OATL4 PAHT SLC22A11 SLC22A12 SLC22A6 SLC22A7 SLC22A8 URAT1	Homo sapiens (human)
Late Phase of HIV Life Cycle	Glycylpeptide N-tetradecanoyltransferase 1 Protein Nef	P04601 P30419	NMT NMT1 nef	Homo sapiens (human)
NOSIP mediated eNOS trafficking	Nitric oxide synthase 3 Nitric oxide synthase-interacting protein	P29474 Q9Y314	NOS3 NOSIP	Homo sapiens (human)
Defective PNP disrupts phosphorolysis of (deoxy)guanosine and (deoxy)inosine	Purine nucleoside phosphorylase	P00491	NP PNP	Homo sapiens (human)
Type II Na+/Pi cotransporters	Sodium-dependent phosphate transport protein 2A Sodium-dependent phosphate transport protein 2B Sodium-dependent phosphate transport protein 2C	O95436 Q06495 Q8N130	NPT2 NPT2C NPTIIC SLC17A2 SLC34A1 SLC34A2 SLC34A3	Homo sapiens (human)
Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)	Sodium-dependent phosphate transport protein 2A	Q06495	NPT2 SLC17A2 SLC34A1	Homo sapiens (human)
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)	Sodium-dependent phosphate transport protein 2C	Q8N130	NPT2C NPTIIC SLC34A3	Homo sapiens (human)

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