GlyCosmos Portal

Displaying entries **17701 - 17725** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9UBS4	DnaJ homolog subfamily B member 11	DNAJB11 EDJ ERJ3 HDJ9	3	11
Q9Y2G5	GDP-fucose protein O-fucosyltransferase 2	POFUT2 C21orf80 FUT13 KIAA0958	3	11	Peters plus syndrome congenital disorder of glycosylation malaria popliteal pterygium syndrome schizophrenia
Q9Y6M7	Sodium bicarbonate cotransporter 3	SLC4A7 BT NBC2 NBC2B NBC3 NBCn1 SBC2 SLC4A6	10	11
P02774	Vitamin D-binding protein	GC	2	11
Q2M3T9	Hyaluronidase-4	HYAL4	5	11	oxyphilic adenoma renal oncocytoma
O75071	EF-hand calcium-binding domain-containing protein 14	EFCAB14 KIAA0494	9	11
P07093	Glia-derived nexin	SERPINE2 PI7 PN1	5	12
Q96DT5	Dynein axonemal heavy chain 11	DNAH11	2	12
P42702	Leukemia inhibitory factor receptor	LIFR	22	12
Q9P232	Contactin-3	CNTN3 KIAA1496 PANG	13	12	ACTH-secreting pituitary adenoma Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Raynaud disease Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 allergic contact dermatitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autistic disorder branchiootic syndrome breast cancer breast carcinoma cancer cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia chronic kidney disease colitis cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease depressive disorder diarrhea dilated cardiomyopathy 1B distal arthrogryposis dry eye syndrome dysthymic disorder embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy fibromyalgia gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis high grade glioma hypertension hypertrophic cardiomyopathy ileitis ileocolitis kidney disease long QT syndrome major depressive disorder melancholic depression morbid obesity mosaic variegated aneuploidy syndrome 1 nephritis nephrosis neurotic disorder obesity obsolete melancholia orofaciodigital syndrome I orofaciodigital syndrome X paraplegia parapsoriasis peripheral artery disease phobic disorder pituitary-dependent Cushing's disease pityriasis rubra pilaris post-traumatic stress disorder prolactinoma psoriasis pustulosis of palm and sole pyoureter restless legs syndrome spinal cord disease trichohepatoenteric syndrome 1 trichohepatoenteric syndrome xerophthalmia
P28068	HLA class II histocompatibility antigen, DM beta chain	HLA-DMB DMB RING7	1	12
Q8WXG9	Adhesion G-protein coupled receptor V1	ADGRV1 GPR98 KIAA0686 KIAA1943 MASS1 VLGR1	34	12
P21333	Filamin-A	FLNA FLN FLN1	18	12
Q6QNK2	Adhesion G-protein coupled receptor D1	ADGRD1 GPR133 PGR25	10	12
O75477	Erlin-1	ERLIN1 C10orf69 KE04 KEO4 SPFH1	3	12
Q9P2G4	Microtubule-associated protein 10	MAP10 KIAA1383 MTR120	1	12
Q86YB8	ERO1-like protein beta	ERO1B ERO1LB	4	12
Q6UWU2	Beta-galactosidase-1-like protein	GLB1L	5	12
Q9NYU1	UDP-glucose:glycoprotein glucosyltransferase 2	UGGT2 UGCGL2 UGT2	4	12	acute myocardial infarction cancer coronary thrombosis diabetes mellitus embryoma myocardial infarction silent myocardial infarction type 2 diabetes mellitus
Q8WWB7	Glycosylated lysosomal membrane protein	GLMP C1orf85	5	12
P30825	High affinity cationic amino acid transporter 1	SLC7A1 ATRC1 ERR REC1L	2	12
P78423	Fractalkine	CX3CL1 FKN NTT SCYD1	13	12
Q13586	Stromal interaction molecule 1	STIM1 GOK	8	12
P14923	Junction plakoglobin	JUP CTNNG DP3	6	12
Q15758	Neutral amino acid transporter B(0)	SLC1A5 ASCT2 M7V1 RDR RDRC	2	12

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