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 **1626 - 1650** of **2090** in total

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Pathway Name ▼	Protein Name	UniProt ID	Gene Symbol	Organism
Defective RIPK1-mediated regulated necrosis	Caspase-8 FAS-associated death domain protein Receptor-interacting serine/threonine-protein kinase 1 TNF receptor-associated factor 2 Tumor necrosis factor receptor type 1-associated DEATH domain protein	Q12933 Q13158 Q13546 Q14790 Q15628	CASP8 FADD MCH5 MORT1 RIP RIP1 RIPK1 TRADD TRAF2 TRAP3	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 POMT2 causes MDDGA2, MDDGB2 and MDDGC2	Dystroglycan 1 Protein O-mannosyl-transferase 1 Protein O-mannosyl-transferase 2	Q14118 Q9UKY4 Q9Y6A1	DAG1 POMT1 POMT2	Homo sapiens (human)
Defective POMT1 causes MDDGA1, MDDGB1 and MDDGC1	Dystroglycan 1 Protein O-mannosyl-transferase 1 Protein O-mannosyl-transferase 2	Q14118 Q9UKY4 Q9Y6A1	DAG1 POMT1 POMT2	Homo sapiens (human)
Defective POMGNT1 causes MDDGA3, MDDGB3 and MDDGC3	Dystroglycan 1 Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1	Q14118 Q8WZA1	DAG1 MGAT1.2 POMGNT1	Homo sapiens (human)
Defective PNP disrupts phosphorolysis of (deoxy)guanosine and (deoxy)inosine	Purine nucleoside phosphorylase	P00491	NP PNP	Homo sapiens (human)
Defective PMM2 causes CDG-1a	Phosphomannomutase 2	O15305	PMM2	Homo sapiens (human)
Defective PGM1 causes CDG1t	Phosphoglucomutase-1	P36871	PGM1	Homo sapiens (human)
Defective PAPSS2 causes SEMD-PA	Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 2	O95340	ATPSK2 PAPSS2	Homo sapiens (human)
Defective OPLAH causes OPLAHD	5-oxoprolinase	O14841	OPLAH	Homo sapiens (human)
Defective NEU1 causes sialidosis	Beta-galactosidase Lysosomal protective protein Sialidase-1	P10619 P16278 Q99519	CTSA ELNR1 GLB1 NANH NEU1 PPGB	Homo sapiens (human)
Defective Mismatch Repair Associated With PMS2	DNA mismatch repair protein Mlh1 Mismatch repair endonuclease PMS2	P40692 P54278	COCA2 MLH1 PMS2 PMSL2	Homo sapiens (human)
Defective Mismatch Repair Associated With MSH6	DNA mismatch repair protein Msh2 DNA mismatch repair protein Msh6	P43246 P52701	GTBP MSH2 MSH6	Homo sapiens (human)
Defective Mismatch Repair Associated With MSH3	DNA mismatch repair protein Msh2 DNA mismatch repair protein Msh3	P20585 P43246	DUC1 DUG MSH2 MSH3	Homo sapiens (human)
Defective Mismatch Repair Associated With MSH2	DNA mismatch repair protein Msh2 DNA mismatch repair protein Msh3 DNA mismatch repair protein Msh6	P20585 P43246 P52701	DUC1 DUG GTBP MSH2 MSH3 MSH6	Homo sapiens (human)
Defective Mismatch Repair Associated With MLH1	DNA mismatch repair protein Mlh1 Mismatch repair endonuclease PMS2	P40692 P54278	COCA2 MLH1 PMS2 PMSL2	Homo sapiens (human)
Defective MUT causes MMAM	Methylmalonic aciduria type A protein, mitochondrial Methylmalonyl-CoA mutase, mitochondrial	P22033 Q8IVH4	MMAA MMUT MUT	Homo sapiens (human)
Defective MTRR causes HMAE	Methionine synthase reductase Methionine synthase	Q99707 Q9UBK8	MTR MTRR	Homo sapiens (human)
Defective MTR causes HMAG	Methionine synthase reductase Methionine synthase	Q99707 Q9UBK8	MTR MTRR	Homo sapiens (human)
Defective MPI causes CDG-1b	Mannose-6-phosphate isomerase	P34949	MPI PMI1	Homo sapiens (human)
Defective MPDU1 causes CDG-1f	Mannose-P-dolichol utilization defect 1 protein	O75352	MPDU1	Homo sapiens (human)
Defective MOGS causes CDG-2b	Mannosyl-oligosaccharide glucosidase	Q13724	GCS1 MOGS	Homo sapiens (human)
Defective MMAB causes MMA, cblB type	Corrinoid adenosyltransferase MMAB	Q96EY8	MMAB	Homo sapiens (human)
Defective MMAA causes MMA, cblA type	Methylmalonic aciduria type A protein, mitochondrial Methylmalonyl-CoA mutase, mitochondrial	P22033 Q8IVH4	MMAA MMUT MUT	Homo sapiens (human)
Defective MGAT2 causes CDG-2a	Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Q10469	MGAT2	Homo sapiens (human)

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