GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **1776 - 1800** of **2090** in total

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Pathway Name	Protein Name	UniProt ID ▲	Gene Symbol
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
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
Signaling by FGFR2 amplification mutants	Fibroblast growth factor receptor 2	P21802	BEK FGFR2 KGFR KSAM
Signaling by FGFR2 fusions	Fibroblast growth factor receptor 2	P21802	BEK FGFR2 KGFR KSAM
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
Defective MMAA causes MMA, cblA type	Methylmalonic aciduria type A protein, mitochondrial Methylmalonyl-CoA mutase, mitochondrial	P22033 Q8IVH4	MMAA MMUT MUT
Defective MUT causes MMAM	Methylmalonic aciduria type A protein, mitochondrial Methylmalonyl-CoA mutase, mitochondrial	P22033 Q8IVH4	MMAA MMUT MUT
MPS II - Hunter syndrome	Iduronate 2-sulfatase	P22304	IDS SIDS
Defective UGT1A1 causes hyperbilirubinemia	UDP-glucuronosyltransferase 1A1	P22309	GNT1 UGT1 UGT1A1
Defective UGT1A4 causes hyperbilirubinemia	UDP-glucuronosyltransferase 1A4	P22310	GNT1 UGT1 UGT1A4
FGFR4 mutant receptor activation	Fibroblast growth factor receptor 4	P22455	FGFR4 JTK2 TKF
Signaling by FGFR3 fusions in cancer	Fibroblast growth factor receptor 3	P22607	FGFR3 JTK4
t(4;14) translocations of FGFR3	Fibroblast growth factor receptor 3	P22607	FGFR3 JTK4
COX reactions	Prostaglandin G/H synthase 1	P23219	COX1 PTGS1
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
Metabolism of ingested SeMet, Sec, MeSec into H2Se	Adenosylhomocysteinase Cystathionine beta-synthase Cystathionine gamma-lyase Glycine N-methyltransferase Histamine N-methyltransferase Nicotinamide N-methyltransferase S-adenosylmethionine synthase isoform type-1 Selenocysteine lyase	P23526 P32929 P35520 P40261 P50135 Q00266 Q14749 Q96I15	AHCY AMS1 CBS CTH GNMT HNMT MAT1A MATA1 NNMT SAHH SCL SCLY
Sulfur amino acid metabolism	Adenosylhomocysteinase Betaine--homocysteine S-methyltransferase 1 Methionine synthase reductase Methionine synthase S-adenosylmethionine synthase isoform type-1 S-methylmethionine--homocysteine S-methyltransferase BHMT2	P23526 Q00266 Q93088 Q99707 Q9H2M3 Q9UBK8	AHCY AMS1 BHMT BHMT2 MAT1A MATA1 MTR MTRR SAHH
Defective AHCY causes HMAHCHD	Adenosylhomocysteinase	P23526	AHCY SAHH
Activated NTRK2 signals through PI3K	BDNF/NT-3 growth factors receptor Brain-derived neurotrophic factor GRB2-associated-binding protein 1 Neurotrophin-4 Phosphatidylinositol 3-kinase regulatory subunit alpha Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform	P23560 P27986 P34130 P42336 Q13480 Q16620	BDNF GAB1 GRB1 NTF4 NTF5 NTRK2 PIK3CA PIK3R1 TRKB
Activated NTRK2 signals through CDK5	BDNF/NT-3 growth factors receptor Brain-derived neurotrophic factor Cyclin-dependent kinase 5 activator 1 Cyclin-dependent kinase 5 Ras-related C3 botulinum toxin substrate 1 Rho guanine nucleotide exchange factor TIAM1	P23560 P63000 Q00535 Q13009 Q15078 Q16620	BDNF CDK5 CDK5R CDK5R1 CDKN5 NCK5A NTRK2 PSSALRE RAC1 TC25 TIAM1 TRKB
NTRK2 activates RAC1	BDNF/NT-3 growth factors receptor Brain-derived neurotrophic factor Dedicator of cytokinesis protein 3 Ras-related C3 botulinum toxin substrate 1	P23560 P63000 Q16620 Q8IZD9	BDNF DOCK3 KIAA0299 MOCA NTRK2 RAC1 TC25 TRKB
BDNF activates NTRK2 (TRKB) signaling	BDNF/NT-3 growth factors receptor Brain-derived neurotrophic factor	P23560 Q16620	BDNF NTRK2 TRKB
Toxicity of botulinum toxin type F (botF)	Botulinum neurotoxin type F Synaptic vesicle glycoprotein 2A Synaptic vesicle glycoprotein 2B Synaptic vesicle glycoprotein 2C Vesicle-associated membrane protein 1 Vesicle-associated membrane protein 2	P23763 P30996 P63027 Q496J9 Q7L0J3 Q7L1I2	KIAA0735 KIAA0736 KIAA1054 SV2A SV2B SV2C SYB1 SYB2 VAMP1 VAMP2 botF
Defective SLC6A2 causes orthostatic intolerance (OI)	Sodium-dependent noradrenaline transporter	P23975	NAT1 NET1 SLC6A2 SLC6A5
Eukaryotic Translation Elongation	Elongation factor 1-alpha 1 Elongation factor 1-alpha 2 Elongation factor 1-beta Elongation factor 1-delta Elongation factor 1-gamma Putative elongation factor 1-alpha-like 3	P24534 P26641 P29692 P68104 Q05639 Q5VTE0	EEF1A EEF1A1 EEF1A1P5 EEF1A2 EEF1AL EEF1AL3 EEF1B EEF1B2 EEF1D EEF1G EF1A EF1B EF1D EF1G LENG7 STN

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