GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **476 - 500** of **2090** in total

« First

‹ Prev

…

16

17

18

19

20

21

22

23

24

…

Next ›

Last »
Pathway Name ▲	Protein Name	UniProt ID	Gene Symbol	GlyTouCan ID
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)	Sodium-dependent phosphate transporter 2	Q08357	GLVR2 PIT2 SLC20A2
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)	Solute carrier family 22 member 12	Q96S37	OATL4 SLC22A12 URAT1
Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)	Organic cation/carnitine transporter 2	O76082	OCTN2 SLC22A5
Defective SLC24A1 causes congenital stationary night blindness 1D (CSNB1D)	Sodium/potassium/calcium exchanger 1	O60721	KIAA0702 NCKX1 SLC24A1
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)	Sodium/potassium/calcium exchanger 4	Q8NFF2	NCKX4 SLC24A4
Defective SLC26A2 causes chondrodysplasias	Sulfate transporter	P50443	DTD DTDST SLC26A2
Defective SLC26A3 causes congenital secretory chloride diarrhea 1 (DIAR1)	Chloride anion exchanger	P40879	DRA SLC26A3
Defective SLC26A4 causes Pendred syndrome (PDS)	Pendrin	O43511	PDS SLC26A4
Defective SLC29A3 causes histiocytosis-lymphadenopathy plus syndrome (HLAS)	Equilibrative nucleoside transporter 3	Q9BZD2	ENT3 SLC29A3
Defective SLC2A1 causes GLUT1 deficiency syndrome 1 (GLUT1DS1)	Solute carrier family 2, facilitated glucose transporter member 1	P11166	GLUT1 SLC2A1	G58161NS
Defective SLC2A10 causes arterial tortuosity syndrome (ATS)	Solute carrier family 2, facilitated glucose transporter member 10	O95528	GLUT10 SLC2A10	G58161NS
Defective SLC2A2 causes Fanconi-Bickel syndrome (FBS)	Solute carrier family 2, facilitated glucose transporter member 2	P11168	GLUT2 SLC2A2	G58161NS G93924TT
Defective SLC2A9 causes hypouricemia renal 2 (RHUC2)	Solute carrier family 2, facilitated glucose transporter member 9	Q9NRM0	GLUT9 SLC2A9	G58161NS
Defective SLC33A1 causes spastic paraplegia 42 (SPG42)	Acetyl-coenzyme A transporter 1	O00400	ACATN AT1 SLC33A1
Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)	Sodium-dependent phosphate transport protein 2A	Q06495	NPT2 SLC17A2 SLC34A1
Defective SLC34A2 causes PALM	Sodium-dependent phosphate transport protein 2B	O95436	SLC34A2
Defective SLC34A2 causes pulmonary alveolar microlithiasis (PALM)	Sodium-dependent phosphate transport protein 2B	O95436	SLC34A2
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)	Sodium-dependent phosphate transport protein 2C	Q8N130	NPT2C NPTIIC SLC34A3
Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)	CMP-sialic acid transporter	P78382	SLC35A1
Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F)	CMP-sialic acid transporter	P78382	SLC35A1
Defective SLC35A3 causes arthrogryposis, mental retardation, and seizures (AMRS)	UDP-N-acetylglucosamine transporter	Q9Y2D2	SLC35A3
Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ)	Zinc transporter ZIP4	Q6P5W5	SLC39A4 ZIP4
Defective SLC3A1 causes cystinuria (CSNU)	Amino acid transporter heavy chain SLC3A1 b(0,+)-type amino acid transporter 1	P82251 Q07837	BAT1 NBAT SLC3A1 SLC7A9
Defective SLC40A1 causes hemochromatosis 4 (HFE4) (duodenum)	Hephaestin Solute carrier family 40 member 1	Q9BQS7 Q9NP59	FPN FPN1 HEPH IREG1 KIAA0698 SLC11A3 SLC40A1
Defective SLC40A1 causes hemochromatosis 4 (HFE4) (macrophages)	Ceruloplasmin Solute carrier family 40 member 1	P00450 Q9NP59	CP FPN FPN1 IREG1 SLC11A3 SLC40A1

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements