GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
O00337	Sodium/nucleoside cotransporter 1	SLC28A1 CNT1	2	0
O43868	Sodium/nucleoside cotransporter 2	SLC28A2 CNT2	2	1
Q9HAS3	Solute carrier family 28 member 3	SLC28A3 CNT3	3	2
Q99808	Equilibrative nucleoside transporter 1	SLC29A1 ENT1	3	11
C8KHU1	Equilibrative nucleoside transporter 1 (Fragment)	SLC29A1	1	0
A0A2U3TZM6	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A2R8Y854	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A2R8Y801	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A2U3TZM5	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A2R8YEH8	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A220K8H0	Solute carrier family 29 member 1 (Augustine blood group)	SLC29A1	1	0
A0A2R8Y6D1	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A2R8YFI6	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A2R8Y567	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
A0A2U3TZJ7	Solute carrier family 29 member 1 (Augustine blood group) (Fragment)	SLC29A1	1	0
Q14542	Equilibrative nucleoside transporter 2	SLC29A2 DER12 ENT2 HNP36	3	0
Q9BZD2	Equilibrative nucleoside transporter 3	SLC29A3 ENT3	1	0
Q7RTT9	Equilibrative nucleoside transporter 4	SLC29A4 ENT4 PMAT	1	0
P11166	Solute carrier family 2, facilitated glucose transporter member 1	SLC2A1 GLUT1	2	9
A6NL68	Solute carrier family 2 member 1 (Fragment)	SLC2A1	1	0
A0A0D9SG74	Solute carrier family 2 member 1 (Fragment)	SLC2A1	1	0
A0A0D9SFK9	Solute carrier family 2 member 1	SLC2A1	1	0
A0A6Q8PFI8	Solute carrier family 2 member 1	SLC2A1	1	0
O95528	Solute carrier family 2, facilitated glucose transporter member 10	SLC2A10 GLUT10	1	0	Hailey-Hailey disease Legg-Calve-Perthes disease Loeys-Dietz syndrome Moyamoya disease Rothmund-Thomson syndrome X-linked dilated cardiomyopathy acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma aortic aneurysm aortic valve disease 2 aortic valve insufficiency aortic valve stenosis arterial tortuosity syndrome asthma autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB blepharophimosis bone disease breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cartilage disease cataract 32 multiple types cerebral infarction cerebrovascular disease childhood type dermatomyositis chondrosarcoma collagen disease congenital central hypoventilation syndrome congenital diaphragmatic hernia congestive heart failure connective tissue disease corneal disease coronary thrombosis craniosynostosis cribriform carcinoma cutis laxa dermatomyositis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy endomyocardial fibrosis esophagitis essential hypertension familial hypertrophic cardiomyopathy gastroesophageal reflux disease granular cell carcinoma hiatus hernia hypertension hypertrophic cardiomyopathy hypertropia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inguinal hernia intellectual disability intermittent claudication interstitial lung disease intrinsic asthma keratoconus learning disability leukocyte adhesion deficiency 1 leukocyte adhesion deficiency lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma mal de Meleda mechanical strabismus megalocornea myocardial infarction myocarditis myopia newborn respiratory distress syndrome obstructive lung disease omphalocele ophthalmoplegia peptic esophagitis peripheral artery disease peripheral vascular disease pneumonia pulmonary emphysema pyloric stenosis respiratory failure restrictive dermopathy scoliosis silent myocardial infarction strabismus thoracic aortic aneurysm tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia vascular disease
Q9BYW1	Solute carrier family 2, facilitated glucose transporter member 11	SLC2A11 GLUT11	1	0

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