GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
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
P37173	TGF-beta receptor type-2	TGFBR2	7	12
P51688	N-sulphoglucosamine sulphohydrolase	SGSH HSS	6	12	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Kearns-Sayre syndrome Kluver-Bucy syndrome Pick's disease Reye syndrome Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome adrenoleukodystrophy ankylosing spondylitis anorexia nervosa arthritis arthropathy beta-mannosidosis cancer cardiomyopathy central nervous system disease central nervous system origin vertigo cerebral degeneration chronic obstructive pulmonary disease cone-rod dystrophy congenital nystagmus depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dissociated nystagmus embryoma endomyocardial fibrosis eosinophilic esophagitis epilepsy fundus albipunctatus fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease major depressive disorder melancholic depression movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis mucosulfatidosis multiple epiphyseal dysplasia narcolepsy nervous system disease neurodegeneration with brain iron accumulation neurodegenerative disease obsolete melancholia osteoarthritis osteochondrodysplasia pathologic nystagmus retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus visual epilepsy
Q969V3	BOS complex subunit NCLN	NCLN	4	12
Q6UXG2	Endosome/lysosome-associated apoptosis and autophagy regulator 1	ELAPOR1 EIG121 KIAA1324	8	12
Q6NSJ0	Myogenesis-regulating glycosidase	MYORG KIAA1161	6	12	amnestic disorder basal ganglia calcification choreatic disease dystonia epilepsy hydrocephalus lingual-facial-buccal dyskinesia microcephaly migraine neurodegenerative disease placental insufficiency recurrent corneal erosion retrograde amnesia secondary Parkinson disease syndromic X-linked intellectual disability type 10 thrombocytopenia visual epilepsy
Q53RD9	Fibulin-7	FBLN7 TM14	6	12
Q9H173	Nucleotide exchange factor SIL1	SIL1	16	12
Q9Y2J2	Band 4.1-like protein 3	EPB41L3 DAL1 KIAA0987	3	12
Q15155	BOS complex subunit NOMO1	NOMO1 PM5	6	12

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