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 **26 - 50** of **2074** in total

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Pathway Name	Protein Name ▼	UniProt ID	Gene Symbol	Organism	GlyTouCan ID
TGFBR2 Kinase Domain Mutants in Cancer	TGF-beta receptor type-1 TGF-beta receptor type-2 Transforming growth factor beta-1 proprotein	P01137 P36897 P37173	ALK5 SKR4 TGFB TGFB1 TGFBR1 TGFBR2	Homo sapiens (human)
Defective SLC26A2 causes chondrodysplasias	Sulfate transporter	P50443	DTD DTDST SLC26A2	Homo sapiens (human)
Metabolism of steroid hormones	Steryl-sulfatase	P08842	ARSC1 STS	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 SLCO1B3 causes hyperbilirubinemia, Rotor type (HBLRR)	Solute carrier organic anion transporter family member 1B3	Q9NPD5	LST2 OATP1B3 OATP8 SLC21A8 SLCO1B3	Homo sapiens (human)
Defective SLCO1B1 causes hyperbilirubinemia, Rotor type (HBLRR)	Solute carrier organic anion transporter family member 1B1	Q9Y6L6	LST1 OATP1B1 OATP2 OATPC SLC21A6 SLCO1B1	Homo sapiens (human)
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)	Solute carrier family 22 member 12	Q96S37	OATL4 SLC22A12 URAT1	Homo sapiens (human)
Defective SLC2A9 causes hypouricemia renal 2 (RHUC2)	Solute carrier family 2, facilitated glucose transporter member 9	Q9NRM0	GLUT9 SLC2A9	Homo sapiens (human)	G58161NS
Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS)	Solute carrier family 2, facilitated glucose transporter member 2	P11168	GLUT2 SLC2A2	Homo sapiens (human)	G58161NS G93924TT
Defective SLC2A10 causes arterial tortuosity syndrome (ATS)	Solute carrier family 2, facilitated glucose transporter member 10	O95528	GLUT10 SLC2A10	Homo sapiens (human)	G58161NS
Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1)	Solute carrier family 2, facilitated glucose transporter member 1	P11166	GLUT1 SLC2A1	Homo sapiens (human)	G58161NS
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 SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN)	Solute carrier family 12 member 6	Q9UHW9	KCC3 SLC12A6	Homo sapiens (human)
Defective SLC12A3 causes Gitelman syndrome (GS)	Solute carrier family 12 member 3	P55017	NCC SLC12A3 TSC	Homo sapiens (human)
Defective SLC12A1 causes Bartter syndrome 1 (BS1)	Solute carrier family 12 member 1	Q13621	NKCC2 SLC12A1	Homo sapiens (human)
Cation-coupled Chloride cotransporters	Solute carrier family 12 member 1 Solute carrier family 12 member 2 Solute carrier family 12 member 3 Solute carrier family 12 member 4 Solute carrier family 12 member 5 Solute carrier family 12 member 6 Solute carrier family 12 member 7	P55011 P55017 Q13621 Q9H2X9 Q9UHW9 Q9UP95 Q9Y666	KCC1 KCC2 KCC3 KCC4 KIAA1176 NCC NKCC1 NKCC2 SLC12A1 SLC12A2 SLC12A3 SLC12A4 SLC12A5 SLC12A6 SLC12A7 TSC	Homo sapiens (human)
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)	Sodium/potassium/calcium exchanger 4	Q8NFF2	NCKX4 SLC24A4	Homo sapiens (human)
Defective SLC24A1 causes congenital stationary night blindness 1D (CSNB1D)	Sodium/potassium/calcium exchanger 1	O60721	KIAA0702 NCKX1 SLC24A1	Homo sapiens (human)
Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)	Sodium/iodide cotransporter	Q92911	NIS SLC5A5	Homo sapiens (human)
Defective SLC9A9 causes autism 16 (AUTS16)	Sodium/hydrogen exchanger 9	Q8IVB4	NHE9 SLC9A9	Homo sapiens (human)
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)	Sodium/hydrogen exchanger 6	Q92581	KIAA0267 NHE6 SLC9A6	Homo sapiens (human)
Sodium/Proton exchangers	Sodium/hydrogen exchanger 1 Sodium/hydrogen exchanger 2 Sodium/hydrogen exchanger 3 Sodium/hydrogen exchanger 4 Sodium/hydrogen exchanger 5 Sodium/hydrogen exchanger 6 Sodium/hydrogen exchanger 7 Sodium/hydrogen exchanger 8 Sodium/hydrogen exchanger 9	P19634 P48764 Q14940 Q6AI14 Q8IVB4 Q92581 Q96T83 Q9UBY0 Q9Y2E8	APNH1 KIAA0267 KIAA0939 NHE1 NHE2 NHE3 NHE4 NHE5 NHE6 NHE7 NHE8 NHE9 SLC9A1 SLC9A2 SLC9A3 SLC9A4 SLC9A5 SLC9A6 SLC9A7 SLC9A8 SLC9A9	Homo sapiens (human)
Defective SLC5A2 causes renal glucosuria (GLYS1)	Sodium/glucose cotransporter 2	P31639	SGLT2 SLC5A2	Homo sapiens (human)	G58161NS
Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM)	Sodium/glucose cotransporter 1	P13866	NAGT SGLT1 SLC5A1	Homo sapiens (human)	G58161NS
Clearance of seratonin	Sodium-dependent serotonin transporter	P31645	HTT SERT SLC6A4	Homo sapiens (human)

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