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 **1676 - 1700** of **2090** in total

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Pathway Name ▼	Protein Name	UniProt ID	Gene Symbol	Organism
Defective F9 activation	Coagulation factor IX Coagulation factor XI Platelet glycoprotein IX Platelet glycoprotein Ib alpha chain Platelet glycoprotein Ib beta chain Platelet glycoprotein V	P00740 P03951 P07359 P13224 P14770 P40197	F11 F9 GP1BA GP1BB GP5 GP9	Homo sapiens (human)
Defective F8 sulfation at Y1699	Coagulation factor VIII Protein-tyrosine sulfotransferase 1 Protein-tyrosine sulfotransferase 2	O60507 O60704 P00451	F8 F8C TPST1 TPST2	Homo sapiens (human)
Defective F8 secretion	Coagulation factor VIII	P00451	F8 F8C	Homo sapiens (human)
Defective F8 cleavage by thrombin	Coagulation factor VIII Prothrombin von Willebrand factor	P00451 P00734 P04275	F2 F8 F8C F8VWF VWF	Homo sapiens (human)
Defective F8 binding to von Willebrand factor	Coagulation factor VIII von Willebrand factor	P00451 P04275	F8 F8C F8VWF VWF	Homo sapiens (human)
Defective F8 binding to the cell membrane	Coagulation factor VIII	P00451	F8 F8C	Homo sapiens (human)
Defective F8 accelerates dissociation of the A2 domain	Coagulation factor VIII	P00451	F8 F8C	Homo sapiens (human)
Defective EXT2 causes exostoses 2	Agrin Basement membrane-specific heparan sulfate proteoglycan core protein Exostosin-1 Exostosin-2 Glypican-1 Glypican-2 Glypican-3 Glypican-4 Glypican-5 Glypican-6 Syndecan-1 Syndecan-2 Syndecan-3 Syndecan-4	O00468 O75056 O75487 P18827 P31431 P34741 P35052 P51654 P78333 P98160 Q16394 Q8N158 Q93063 Q9Y625	AGRIN AGRN EXT1 EXT2 GPC1 GPC2 GPC3 GPC4 GPC5 GPC6 HSPG1 HSPG2 KIAA0468 OCI5 SDC SDC1 SDC2 SDC3 SDC4	Homo sapiens (human)
Defective EXT1 causes exostoses 1, TRPS2 and CHDS	Agrin Basement membrane-specific heparan sulfate proteoglycan core protein Exostosin-1 Exostosin-2 Glypican-1 Glypican-2 Glypican-3 Glypican-4 Glypican-5 Glypican-6 Syndecan-1 Syndecan-2 Syndecan-3 Syndecan-4	O00468 O75056 O75487 P18827 P31431 P34741 P35052 P51654 P78333 P98160 Q16394 Q8N158 Q93063 Q9Y625	AGRIN AGRN EXT1 EXT2 GPC1 GPC2 GPC3 GPC4 GPC5 GPC6 HSPG1 HSPG2 KIAA0468 OCI5 SDC SDC1 SDC2 SDC3 SDC4	Homo sapiens (human)
Defective DPM3 causes CDG-1o	Dolichol phosphate-mannose biosynthesis regulatory protein Dolichol-phosphate mannosyltransferase subunit 1 Dolichol-phosphate mannosyltransferase subunit 3	O60762 O94777 Q9P2X0	DPM1 DPM2 DPM3	Homo sapiens (human)
Defective DPM2 causes CDG-1u	Dolichol phosphate-mannose biosynthesis regulatory protein Dolichol-phosphate mannosyltransferase subunit 1 Dolichol-phosphate mannosyltransferase subunit 3	O60762 O94777 Q9P2X0	DPM1 DPM2 DPM3	Homo sapiens (human)
Defective DPM1 causes CDG-1e	Dolichol phosphate-mannose biosynthesis regulatory protein Dolichol-phosphate mannosyltransferase subunit 1 Dolichol-phosphate mannosyltransferase subunit 3	O60762 O94777 Q9P2X0	DPM1 DPM2 DPM3	Homo sapiens (human)
Defective DPAGT1 causes CDG-1j, CMSTA2	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	Q9H3H5	DPAGT1 DPAGT2	Homo sapiens (human)
Defective DNA double strand break response due to BRCA1 loss of function	BRCA1-associated RING domain protein 1 Breast cancer type 1 susceptibility protein	P38398 Q99728	BARD1 BRCA1 RNF53	Homo sapiens (human)
Defective DNA double strand break response due to BARD1 loss of function	BRCA1-associated RING domain protein 1 Breast cancer type 1 susceptibility protein	P38398 Q99728	BARD1 BRCA1 RNF53	Homo sapiens (human)
Defective DHDDS causes RP59	Dehydrodolichyl diphosphate synthase complex subunit DHDDS Dehydrodolichyl diphosphate synthase complex subunit NUS1	Q86SQ9 Q96E22	C6orf68 DHDDS HDS NGBR NUS1	Homo sapiens (human)
Defective CYP1B1 causes Glaucoma	Cytochrome P450 1B1	Q16678	CYP1B1	Homo sapiens (human)
Defective CYP17A1 causes AH5	Steroid 17-alpha-hydroxylase/17,20 lyase	P05093	CYP17 CYP17A1 S17AH	Homo sapiens (human)
Defective CYP11A1 causes AICSR	Adrenodoxin, mitochondrial Cholesterol side-chain cleavage enzyme, mitochondrial Ferredoxin-2, mitochondrial NADPH	P05108 P10109 P22570 Q6P4F2	ADX ADXR CYP11A CYP11A1 FDX1 FDX1L FDX2 FDXR	Homo sapiens (human)
Defective CUBN causes MGA1	Cobalamin binding intrinsic factor Cubilin Protein amnionless	O60494 P27352 Q9BXJ7	AMN CBLIF CUBN GIF IFCR IFMH	Homo sapiens (human)
Defective CSF2RB causes SMDP5	Cytokine receptor common subunit beta Granulocyte-macrophage colony-stimulating factor receptor subunit alpha Pulmonary surfactant-associated protein A1 Pulmonary surfactant-associated protein A2 Pulmonary surfactant-associated protein B Pulmonary surfactant-associated protein D Surfactant protein C Surfactant-associated protein 3	P07988 P0C7M3 P11686 P15509 P32927 P35247 Q8IWL1 Q8IWL2	COLEC4 COLEC5 COLEC7 CSF2R CSF2RA CSF2RB CSF2RY IL3RB IL5RB PSAP PSPD SFTA3 SFTP1 SFTP2 SFTP3 SFTP4 SFTPA SFTPA1 SFTPA1B SFTPA2 SFTPA2B SFTPB SFTPC SFTPD SFTPH	Homo sapiens (human)
Defective CSF2RA causes SMDP4	Cytokine receptor common subunit beta Granulocyte-macrophage colony-stimulating factor receptor subunit alpha Pulmonary surfactant-associated protein A1 Pulmonary surfactant-associated protein A2 Pulmonary surfactant-associated protein B Pulmonary surfactant-associated protein D Surfactant protein C Surfactant-associated protein 3	P07988 P0C7M3 P11686 P15509 P32927 P35247 Q8IWL1 Q8IWL2	COLEC4 COLEC5 COLEC7 CSF2R CSF2RA CSF2RB CSF2RY IL3RB IL5RB PSAP PSPD SFTA3 SFTP1 SFTP2 SFTP3 SFTP4 SFTPA SFTPA1 SFTPA1B SFTPA2 SFTPA2B SFTPB SFTPC SFTPD SFTPH	Homo sapiens (human)
Defective CP causes aceruloplasminemia (ACERULOP)	Ceruloplasmin Solute carrier family 40 member 1	P00450 Q9NP59	CP FPN FPN1 IREG1 SLC11A3 SLC40A1	Homo sapiens (human)
Defective CHSY1 causes TPBS	Biglycan Brevican core protein Chondroitin sulfate proteoglycan 4 Chondroitin sulfate proteoglycan 5 Chondroitin sulfate synthase 1 Decorin Neurocan core protein Versican core protein	O14594 O95196 P07585 P13611 P21810 Q6UVK1 Q86X52 Q96GW7	BCAN BEHAB BGN CALEB CHSY CHSY1 CSPG2 CSPG3 CSPG4 CSPG5 CSPG7 CSS1 DCN KIAA0990 MCSP NCAN NEUR NGC SLRR1A SLRR1B VCAN	Homo sapiens (human)
Defective CHST6 causes MCDC1	Aggrecan core protein Carbohydrate sulfotransferase 6 Fibromodulin Keratocan Lumican Mimecan Osteomodulin Prolargin	O60938 P16112 P20774 P51884 P51888 Q06828 Q99983 Q9GZX3	ACAN AGC1 CHST6 CSPG1 FM FMOD KERA LDC LUM MSK16 OGN OIF OMD PRELP SLRR2A SLRR2B SLRR2C SLRR2D SLRR2E SLRR3A	Homo sapiens (human)

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