GlyCosmos Portal

Displaying entries **15776 - 15800** of **18496** in total

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
B5A937	Soluble MET variant 9	MET	4	0
Q8WVQ1	Soluble calcium-activated nucleotidase 1	CANT1 SHAPY	2	5
A1L4H1	Soluble scavenger receptor cysteine-rich domain-containing protein SSC5D	SSC5D	26	8
G3XAL9	Solute carrier family 12 (Sodium/potassium/chloride transporters), member 2, isoform CRA_a	SLC12A2	2	0
Q13621	Solute carrier family 12 member 1	SLC12A1 NKCC2	2	1
P55011	Solute carrier family 12 member 2	SLC12A2 NKCC1	3	6
P55017	Solute carrier family 12 member 3	SLC12A3 NCC TSC	2	0
Q9UP95	Solute carrier family 12 member 4	SLC12A4 KCC1	5	7
Q9H2X9	Solute carrier family 12 member 5	SLC12A5 KCC2 KIAA1176	4	0
Q9UHW9	Solute carrier family 12 member 6	SLC12A6 KCC3	4	3
Q9Y666	Solute carrier family 12 member 7	SLC12A7 KCC4	3	7
A0AV02	Solute carrier family 12 member 8	SLC12A8 CCC9	1	0
Q9BXP2	Solute carrier family 12 member 9	SLC12A9 CCC6 CIP1	2	3
Q9BZW2	Solute carrier family 13 member 1	SLC13A1 NAS1 NASI1	3	0
P46059	Solute carrier family 15 member 1	SLC15A1 PEPT1	7	0
Q16348	Solute carrier family 15 member 2	SLC15A2 PEPT2	5	0
Q8IY34	Solute carrier family 15 member 3	SLC15A3 OCTP PHT2 PTR3	6	0
Q8N697	Solute carrier family 15 member 4	SLC15A4 PHT1 PTR4	2	3
A0A0D9SFK9	Solute carrier family 2 member 1	SLC2A1	1	0
A0A6Q8PFI8	Solute carrier family 2 member 1	SLC2A1	1	0
A6NL68	Solute carrier family 2 member 1 (Fragment)	SLC2A1	1	0
A0A0D9SG74	Solute carrier family 2 member 1 (Fragment)	SLC2A1	1	0
P11166	Solute carrier family 2, facilitated glucose transporter member 1	SLC2A1 GLUT1	2	9
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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