GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q9HBD1	Roquin-2	RC3H2 MNAB RNF164	25	2
P12270	Nucleoprotein TPR	TPR	25	3
Q96HA1	Nuclear envelope pore membrane protein POM 121	POM121 KIAA0618 NUP121 POM121A	25	1
Q92793	CREB-binding protein	CREBBP CBP	25	2
P08047	Transcription factor Sp1	SP1 TSFP1	25	2
Q9UGU0	Transcription factor 20	TCF20 KIAA0292 SPBP	25	2
Q6UXG3	CMRF35-like molecule 9	CD300LG CLM9 TREM4	25	1
Q9UGM3	Deleted in malignant brain tumors 1 protein	DMBT1 GP340	26	1
Q86YL7	Podoplanin	PDPN GP36	26	4
Q96PK6	RNA-binding protein 14	RBM14 SIP	26	4
Q75N90	Fibrillin-3	FBN3 KIAA1776	26	15
A1L4H1	Soluble scavenger receptor cysteine-rich domain-containing protein SSC5D	SSC5D	26	8
Q86SQ4	Adhesion G-protein coupled receptor G6	ADGRG6 DREG GPR126 VIGR	26	37
Q9NS15	Latent-transforming growth factor beta-binding protein 3	LTBP3	26	8
O15118	NPC intracellular cholesterol transporter 1	NPC1	26	32	Niemann-Pick disease type C1
Q03164	Histone-lysine N-methyltransferase 2A	KMT2A ALL1 CXXC7 HRX HTRX MLL MLL1 TRX1	26	6
P00451	Coagulation factor VIII	F8 F8C	26	61
P12111	Collagen alpha-3(VI) chain	COL6A3	26	97
Q6UXD5	Seizure 6-like protein 2	SEZ6L2 PSK	26	22
Q05707	Collagen alpha-1(XIV) chain	COL14A1 UND	26	108
Q9ULT8	E3 ubiquitin-protein ligase HECTD1	HECTD1 KIAA1131	26	6
O43451	Maltase-glucoamylase	MGAM MGA MGAML	26	110	Duchenne muscular dystrophy Fabry disease Gaucher's disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Japanese encephalitis adenocarcinoma adenoma amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy brachydactyly type C brachydactyly breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease chylomicron retention disease congenital disorder of glycosylation congenital muscular dystrophy coronary artery disease cribriform carcinoma cystic fibrosis cystinuria dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hyperglycemia hypertrophic cardiomyopathy hypoglycemia limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease major depressive disorder melancholic depression muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myotonic dystrophy type 1 myotonic dystrophy type 2 neuromuscular disease nutmeg liver obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete constipation obsolete melancholia oculopharyngeal muscular dystrophy progressive muscular atrophy prolactinoma punctate palmoplantar keratoderma type III rippling muscle disease 2 squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease yellow fever
O00461	Golgi integral membrane protein 4	GOLIM4 GIMPC GOLPH4 GPP130	27	8
Q76LX8	A disintegrin and metalloproteinase with thrombospondin motifs 13	ADAMTS13 C9orf8	27	15
P82279	Protein crumbs homolog 1	CRB1	27	1

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