GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9NRN5	Olfactomedin-like protein 3	OLFML3 PSEC0035 PSEC0173 PSEC0244 UNQ663/PRO1294	3	105
Q92896	Golgi apparatus protein 1	CFR1 ESL1 GLG1 MG160	15	105
Q05707	Collagen alpha-1(XIV) chain	COL14A1 UND	30	106	esophagus squamous cell carcinoma
P01008	Antithrombin-III	AT3 PRO0309 SERPINC1	7	106	antithrombin III deficiency disseminated intravascular coagulation intermediate coronary syndrome thrombosis toxic shock syndrome
Q14108	Lysosome membrane protein 2	CD36L2 LIMP2 LIMPII SCARB2	13	106	progressive myoclonus epilepsy 4
Q6YHK3	CD109 antigen	CD109 CPAMD7	19	107
P11717	Cation-independent mannose-6-phosphate receptor	IGF2R MPRI	35	109	breast carcinoma in situ hepatocellular carcinoma in situ carcinoma nephroblastoma type 1 diabetes mellitus type 2 diabetes mellitus
P05362	Intercellular adhesion molecule 1	ICAM1	12	109	Alzheimer's disease Behcet's disease Crohn's disease Graves ophthalmopathy Graves' disease biliary atresia diabetic retinopathy inflammatory bowel disease iridocyclitis liver cirrhosis malaria multiple myeloma prostate cancer psoriasis skin melanoma type 1 diabetes mellitus
Q9H3G5	Probable serine carboxypeptidase CPVL	CPVL PSEC0124 UNQ197/PRO223 VLP	5	109
O43451	Maltase-glucoamylase	MGA MGAM MGAML	28	110
P08962	CD63 antigen	CD63 MLA1 TSPAN30	6	110
P35555	Fibrillin-1	FBN FBN1	47	110	CREST syndrome Marfan syndrome Weill-Marchesani syndrome acromicric dysplasia aortic aneurysm autosomal dominant isolated ectopia lentis 1 geleophysic dysplasia 2 mitral valve prolapse mixed connective tissue disease scoliosis stiff skin syndrome systemic scleroderma
P00750	Tissue-type plasminogen activator	PLAT	7	110	antiphospholipid syndrome diabetic angiopathy factor VIII deficiency myocardial infarction osteonecrosis peritonitis type 2 diabetes mellitus von Willebrand's disease 1
Q14112	Nidogen-2	NID2	39	112
O43852	Calumenin	CALU	11	113
P24043	Laminin subunit alpha-2	LAMA2 LAMM	34	113	autosomal recessive limb-girdle muscular dystrophy congenital merosin-deficient muscular dystrophy 1A muscular dystrophy myopia
P12821	Angiotensin-converting enzyme	ACE DCP DCP1	23	113	Behcet's disease COVID-19 Coronavirus infectious disease Fabry disease IgA glomerulonephritis IgA vasculitis allergic disease anemia ankylosing spondylitis aspiration pneumonia asthma atrial fibrillation breast cancer cerebral infarction chronic obstructive pulmonary disease coronary artery disease diabetic retinopathy diastolic heart failure end stage renal disease familial Mediterranean fever gallbladder adenocarcinoma heart valve disease hepatitis A hepatocellular carcinoma hypertension leukemia liver cirrhosis lung cancer mitral valve disease mitral valve prolapse multiple myeloma myocardial infarction nephritis non-arteritic anterior ischemic optic neuropathy obstructive sleep apnea pneumonia polycythemia pre-eclampsia proteinuria sarcoidosis stomach cancer subacute sclerosing panencephalitis toxic shock syndrome type 1 diabetes mellitus type 2 diabetes mellitus
P56199	Integrin alpha-1	ITGA1	29	113
P01215	Glycoprotein hormones alpha chain	CGA	4	114
P08648	Integrin alpha-5	FNRA ITGA5	18	115
P12110	Collagen alpha-2(VI) chain	COL6A2	9	115	Bethlem myopathy Ullrich congenital muscular dystrophy 1B
P07339	Cathepsin D	CPSD CTSD	12	115	Alzheimer's disease breast cancer neuronal ceroid lipofuscinosis 10
P15586	N-acetylglucosamine-6-sulfatase	GNS	22	116	mucopolysaccharidosis III mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID
P55083	Microfibril-associated glycoprotein 4	MFAP4	3	118
P05026	Sodium/potassium-transporting ATPase subunit beta-1	ATP1B ATP1B1	5	120	essential hypertension

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