GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

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

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9UBS4	DnaJ homolog subfamily B member 11	DNAJB11 EDJ ERJ3 HDJ9	Homo sapiens (human)	3	11
Q9Y2G5	GDP-fucose protein O-fucosyltransferase 2	POFUT2 C21orf80 FUT13 KIAA0958	Homo sapiens (human)	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	Homo sapiens (human)	10	11
P02774	Vitamin D-binding protein	GC	Homo sapiens (human)	2	11
Q2M3T9	Hyaluronidase-4	HYAL4	Homo sapiens (human)	5	11	oxyphilic adenoma renal oncocytoma
O75071	EF-hand calcium-binding domain-containing protein 14	EFCAB14 KIAA0494	Homo sapiens (human)	9	11
P07093	Glia-derived nexin	SERPINE2 PI7 PN1	Homo sapiens (human)	5	12
Q96DT5	Dynein axonemal heavy chain 11	DNAH11	Homo sapiens (human)	2	12
P42702	Leukemia inhibitory factor receptor	LIFR	Homo sapiens (human)	22	12
Q9P232	Contactin-3	CNTN3 KIAA1496 PANG	Homo sapiens (human)	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	Homo sapiens (human)	1	12
Q8WXG9	Adhesion G-protein coupled receptor V1	ADGRV1 GPR98 KIAA0686 KIAA1943 MASS1 VLGR1	Homo sapiens (human)	34	12
P21333	Filamin-A	FLNA FLN FLN1	Homo sapiens (human)	18	12
Q6QNK2	Adhesion G-protein coupled receptor D1	ADGRD1 GPR133 PGR25	Homo sapiens (human)	10	12
O75477	Erlin-1	ERLIN1 C10orf69 KE04 KEO4 SPFH1	Homo sapiens (human)	3	12
Q9P2G4	Microtubule-associated protein 10	MAP10 KIAA1383 MTR120	Homo sapiens (human)	1	12
Q86YB8	ERO1-like protein beta	ERO1B ERO1LB	Homo sapiens (human)	4	12
Q6UWU2	Beta-galactosidase-1-like protein	GLB1L	Homo sapiens (human)	5	12
Q9NYU1	UDP-glucose:glycoprotein glucosyltransferase 2	UGGT2 UGCGL2 UGT2	Homo sapiens (human)	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	Homo sapiens (human)	5	12
P30825	High affinity cationic amino acid transporter 1	SLC7A1 ATRC1 ERR REC1L	Homo sapiens (human)	2	12
P78423	Fractalkine	CX3CL1 FKN NTT SCYD1	Homo sapiens (human)	13	12
Q13586	Stromal interaction molecule 1	STIM1 GOK	Homo sapiens (human)	8	12
P14923	Junction plakoglobin	JUP CTNNG DP3	Homo sapiens (human)	6	12
Q15758	Neutral amino acid transporter B(0)	SLC1A5 ASCT2 M7V1 RDR RDRC	Homo sapiens (human)	2	12

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