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 **476 - 500** of **2074** in total

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Pathway Name ▲	Protein Name	UniProt ID	Gene Symbol	Organism	GlyTouCan ID
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 SLC2A9 causes hypouricemia renal 2 (RHUC2)	Solute carrier family 2, facilitated glucose transporter member 9	Q9NRM0	GLUT9 SLC2A9	Homo sapiens (human)	G58161NS
Defective SLC33A1 causes spastic paraplegia 42 (SPG42)	Acetyl-coenzyme A transporter 1	O00400	ACATN AT1 SLC33A1	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 SLC34A2 causes PALM	Sodium-dependent phosphate transport protein 2B	O95436	SLC34A2	Homo sapiens (human)
Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)	Sodium-dependent phosphate transport protein 2B	O95436	SLC34A2	Homo sapiens (human)
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)	Sodium-dependent phosphate transport protein 2C	Q8N130	NPT2C NPTIIC SLC34A3	Homo sapiens (human)
Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ)	Zinc transporter ZIP4	Q6P5W5	SLC39A4 ZIP4	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 SLC40A1 causes hemochromatosis 4 (HFE4) (duodenum)	Ferroportin Hephaestin	Q9BQS7 Q9NP59	FPN FPN1 HEPH IREG1 KIAA0698 SLC11A3 SLC40A1	Homo sapiens (human)
Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages)	Ceruloplasmin Ferroportin	P00450 Q9NP59	CP FPN FPN1 IREG1 SLC11A3 SLC40A1	Homo sapiens (human)
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA)	Band 3 anion transport protein	P02730	AE1 DI EPB3 SLC4A1	Homo sapiens (human)
Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA)	Electrogenic sodium bicarbonate cotransporter 1	Q9Y6R1	NBC NBC1 NBCE1 SLC4A4	Homo sapiens (human)
Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM)	Sodium/glucose cotransporter 1	P13866	NAGT SGLT1 SLC5A1	Homo sapiens (human)	G58161NS
Defective SLC5A2 causes renal glucosuria (GLYS1)	Sodium/glucose cotransporter 2	P31639	SGLT2 SLC5A2	Homo sapiens (human)	G58161NS
Defective SLC5A5 causes thyroid dyshormonogenesis 1 (TDH1)	Sodium/iodide cotransporter	Q92911	NIS SLC5A5	Homo sapiens (human)
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)	High affinity choline transporter 1	Q9GZV3	CHT1 SLC5A7	Homo sapiens (human)
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)	High affinity choline transporter 1	Q9GZV3	CHT1 SLC5A7	Homo sapiens (human)
Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria	Inactive sodium-dependent neutral amino acid transporter B(0)AT3	Q96N87	B0AT3 SLC6A18 XTRP2	Homo sapiens (human)
Defective SLC6A18 may confer susceptibility to iminoglycinuria and/or hyperglycinuria	Inactive sodium-dependent neutral amino acid transporter B(0)AT3	Q96N87	B0AT3 SLC6A18 XTRP2	Homo sapiens (human)
Defective SLC6A19 causes Hartnup disorder (HND)	Sodium-dependent neutral amino acid transporter B(0)AT1	Q695T7	B0AT1 SLC6A19	Homo sapiens (human)
Defective SLC6A19 causes Hartnup disorder (HND)	Sodium-dependent neutral amino acid transporter B(0)AT1	Q695T7	B0AT1 SLC6A19	Homo sapiens (human)
Defective SLC6A2 causes orthostatic intolerance (OI)	Sodium-dependent noradrenaline transporter	P23975	NAT1 NET1 SLC6A2 SLC6A5	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)

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