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 **1951 - 1975** of **2090** in total

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Pathway Name	Protein Name	UniProt ID ▲	Gene Symbol	Organism
Transport of nucleotide sugars	Adenosine 3'-phospho 5'-phosphosulfate transporter 1 Adenosine 3'-phospho 5'-phosphosulfate transporter 2 CMP-sialic acid transporter GDP-fucose transporter 1 Nucleotide sugar transporter SLC35B4 Nucleotide sugar transporter SLC35D1 Nucleotide sugar transporter SLC35D2 UDP-N-acetylglucosamine transporter UDP-galactose translocator	P78381 P78382 Q76EJ3 Q8TB61 Q969S0 Q96A29 Q9H1N7 Q9NTN3 Q9Y2D2	C6orf196 FUCT1 HFRC KIAA0260 PAPST1 PAPST2 SLC35A1 SLC35A2 SLC35A3 SLC35B2 SLC35B3 SLC35B4 SLC35C1 SLC35D1 SLC35D2 UGALT UGT UGTL UGTREL7 UGTREL8 YEA4	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 SLC3A1 causes cystinuria (CSNU)	Amino acid transporter heavy chain SLC3A1 b(0,+)-type amino acid transporter 1	P82251 Q07837	BAT1 NBAT SLC3A1 SLC7A9	Homo sapiens (human)
Defective SLC7A9 causes cystinuria (CSNU)	Amino acid transporter heavy chain SLC3A1 b(0,+)-type amino acid transporter 1	P82251 Q07837	BAT1 NBAT SLC3A1 SLC7A9	Homo sapiens (human)
SMAD4 MH2 Domain Mutants in Cancer	Mothers against decapentaplegic homolog 2 Mothers against decapentaplegic homolog 3 Mothers against decapentaplegic homolog 4	P84022 Q13485 Q15796	DPC4 MADH2 MADH3 MADH4 MADR2 SMAD2 SMAD3 SMAD4	Homo sapiens (human)
SMAD2/3 MH2 Domain Mutants in Cancer	Mothers against decapentaplegic homolog 2 Mothers against decapentaplegic homolog 3 Mothers against decapentaplegic homolog 4	P84022 Q13485 Q15796	DPC4 MADH2 MADH3 MADH4 MADR2 SMAD2 SMAD3 SMAD4	Homo sapiens (human)
Blockage of phagosome acidification	Low molecular weight protein-tyrosine phosphatase A V-type proton ATPase subunit H	P9WIA1 Q9UI12	ATP6V1H mptpA ptpA	Homo sapiens (human)
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)	Sodium-dependent dopamine transporter	Q01959	DAT1 SLC6A3	Homo sapiens (human)
Defective SLC6A3 causes Parkinsonism-dystonia infantile (PKDYS)	Sodium-dependent dopamine transporter	Q01959	DAT1 SLC6A3	Homo sapiens (human)
Neurotransmitter release cycle	N-acylethanolamine-hydrolyzing acid amidase	Q02083	ASAHL NAAA PLT	Homo sapiens (human)
Rhesus glycoproteins mediate ammonium transport.	Ammonium transporter Rh type A Ammonium transporter Rh type B Ammonium transporter Rh type C	Q02094 Q9H310 Q9UBD6	C15orf6 CDRC2 PDRC2 RH50 RHAG RHBG RHCG RHGK	Homo sapiens (human)
Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN)	Ammonium transporter Rh type A	Q02094	RH50 RHAG	Homo sapiens (human)
Defective ACY1 causes encephalopathy	Aminoacylase-1	Q03154	ACY1	Homo sapiens (human)
Defective GFPT1 causes CMSTA1	Glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1	Q06210	GFAT GFPT GFPT1	Homo sapiens (human)
mRNA decay by 3' to 5' exoribonuclease	7-methylguanosine phosphate-specific 5'-nucleotidase Exosome complex component CSL4 Exosome complex component MTR3 Exosome complex component RRP40 Exosome complex component RRP41 Exosome complex component RRP42 Exosome complex component RRP43 Exosome complex component RRP45 Exosome complex component RRP46 Exosome complex component RRP4 Exosome complex exonuclease RRP44 HBS1-like protein Superkiller complex protein 2 Superkiller complex protein 3 Superkiller complex protein 8 m7GpppX diphosphatase	Q06265 Q13868 Q15024 Q15477 Q5RKV6 Q6PGP7 Q969T7 Q96B26 Q96C86 Q9GZS3 Q9NPD3 Q9NQT4 Q9NQT5 Q9Y2L1 Q9Y3B2 Q9Y450	CML28 CSL4 DCPS DCS1 DDX13 DIS3 EXOSC1 EXOSC2 EXOSC3 EXOSC4 EXOSC5 EXOSC6 EXOSC7 EXOSC8 EXOSC9 HBS1 HBS1L HINT5 KIAA0116 KIAA0372 KIAA1008 KIAA1038 MTR3 NT5C3B NT5C3L OIP2 PMSCL1 RRP4 RRP40 RRP41 RRP42 RRP43 RRP44 RRP46 SKI2W SKI6 SKIC2 SKIC3 SKIC8 SKIV2 SKIV2L TTC37 W WDR61	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 Intrinsic Pathway for Apoptosis Due to p14ARF Loss of Function	Complement component 1 Q subcomponent-binding protein, mitochondrial Tumor suppressor ARF	Q07021 Q8N726	C1QBP CDKN2 CDKN2A GC1QBP HABP1 MLM SF2P32	Homo sapiens (human)
Apoptotic factor-mediated response	Complement component 1 Q subcomponent-binding protein, mitochondrial Tumor suppressor ARF	Q07021 Q8N726	C1QBP CDKN2 CDKN2A GC1QBP HABP1 MLM SF2P32	Homo sapiens (human)
NTRK3 as a dependence receptor	Apoptosis regulator BAX NT-3 growth factor receptor Negative elongation factor B	Q07812 Q16288 Q8WX92	BAX BCL2L4 COBRA1 KIAA1182 NELFB NTRK3 TRKC	Homo sapiens (human)
Sodium-coupled phosphate cotransporters	Sodium-dependent phosphate transporter 1 Sodium-dependent phosphate transporter 2	Q08357 Q8WUM9	GLVR1 GLVR2 PIT1 PIT2 SLC20A1 SLC20A2	Homo sapiens (human)
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)	Sodium-dependent phosphate transporter 2	Q08357	GLVR2 PIT2 SLC20A2	Homo sapiens (human)
Conjugation of benzoate with glycine	Acyl-coenzyme A synthetase ACSM1, mitochondrial Acyl-coenzyme A synthetase ACSM2B, mitochondrial Glycine N-acyltransferase-like protein 1 Glycine N-acyltransferase-like protein 2 Glycine N-acyltransferase-like protein 3 Glycine N-acyltransferase	Q08AH1 Q5SZD4 Q68CK6 Q6IB77 Q8WU03 Q969I3	ACGNAT ACSM1 ACSM2 ACSM2B BUCS1 C6orf140 CAT GAT GLYAT GLYATL1 GLYATL2 GLYATL3 GNAT LAE MACS1	Homo sapiens (human)
Conjugation of phenylacetate with glutamine	Acyl-coenzyme A synthetase ACSM1, mitochondrial Acyl-coenzyme A synthetase ACSM2B, mitochondrial	Q08AH1 Q68CK6	ACSM1 ACSM2 ACSM2B BUCS1 LAE MACS1	Homo sapiens (human)
Reactions specific to the hybrid N-glycan synthesis pathway	Beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Q09327	GGNT3 MGAT3	Homo sapiens (human)

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