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	November 12, 2024
ECODAB	April 1, 2019

Displaying entries **2001 - 2025** of **2074** in total

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Pathway Name	Protein Name	UniProt ID	Gene Symbol ▲	Organism
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)
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)
Mitochondrial transcription initiation	DNA-directed RNA polymerase, mitochondrial Dimethyladenosine transferase 2, mitochondrial Transcription factor A, mitochondrial	O00411 Q00059 Q9H5Q4	NS5ATP5 POLRMT TCF6 TCF6L2 TFAM TFB2M	Homo sapiens (human)
NTF3 activates NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Neurotrophin-3	P20783 Q16620	NTF3 NTRK2 TRKB	Homo sapiens (human)
Activated NTRK3 signals through PLCG1	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 NT-3 growth factor receptor Neurotrophin-3	P19174 P20783 Q16288	NTF3 NTRK3 PLC1 PLCG1 TRKC	Homo sapiens (human)
NTF3 activates NTRK3 signaling	NT-3 growth factor receptor Neurotrophin-3	P20783 Q16288	NTF3 NTRK3 TRKC	Homo sapiens (human)
NTF4 activates NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Neurotrophin-4	P34130 Q16620	NTF4 NTF5 NTRK2 TRKB	Homo sapiens (human)
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)	Solute carrier family 22 member 12	Q96S37	OATL4 SLC22A12 URAT1	Homo sapiens (human)
Defective SLCO2A1 causes primary, autosomal recessive hypertrophic osteoarthropathy 2 (PHOAR2)	Solute carrier organic anion transporter family member 2A1	Q92959	OATP2A1 SLC21A2 SLCO2A1	Homo sapiens (human)
Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)	Organic cation/carnitine transporter 2	O76082	OCTN2 SLC22A5	Homo sapiens (human)
Proton/oligopeptide cotransporters	Solute carrier family 15 member 1 Solute carrier family 15 member 3 Solute carrier family 15 member 4	P46059 Q8IY34 Q8N697	OCTP PEPT1 PHT1 PHT2 PTR3 PTR4 SLC15A1 SLC15A3 SLC15A4	Homo sapiens (human)
Defective OPLAH causes OPLAHD	5-oxoprolinase	O14841	OPLAH	Homo sapiens (human)
Defective visual phototransduction due to OPN1LW loss of function	Long-wave-sensitive opsin 1	P04000	OPN1LW RCP	Homo sapiens (human)

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