GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
O60931	Cystinosin	CTNS	7	0	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 Fanconi anemia Fanconi syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia androgen insensitivity syndrome anhidrosis 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 bacterial vaginosis bone disease cartilage disease cerebral degeneration cone-rod dystrophy connective tissue disease cystinosis diabetes mellitus diabetic ketoacidosis disease of metabolism distal myopathy eunuchism exocrine pancreatic insufficiency facioscapulohumeral muscular dystrophy fundus albipunctatus glomerulonephritis hypogonadism hypohidrosis hypokalemia hypophosphatemia kidney disease kidney failure limb-girdle muscular dystrophy lysosomal storage disease male infertility muscular dystrophy nephritis nephrolithiasis nephrosis obsolete asthenopia 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 oculopharyngeal muscular dystrophy osteomalacia premature menopause proteinuria pyoureter recurrent corneal erosion retinal disease retinitis pigmentosa retinitis rickets spondyloepimetaphyseal dysplasia, Sponastrime type uric acid nephrolithiasis vaginitis vulvitis vulvovaginitis
O60934	Nibrin	NBN NBS NBS1 P95	2	2
O60938	Keratocan	KERA SLRR2B	5	3
O60939	Sodium channel subunit beta-2	SCN2B	3	0
O60942	mRNA-capping enzyme	RNGTT CAP1A	0	1
O62900	MHC class I antigen (Fragment)	HLA-B	1	0
O71037	Endogenous retrovirus group K member 19 Env polyprotein	ERVK-19	11	0
O75015	Low affinity immunoglobulin gamma Fc region receptor III-B	FCGR3B CD16B FCG3 FCGR3 IGFR3	6	40	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 B-cell lymphoma Behcet's disease Burkitt lymphoma CINCA Syndrome CREST syndrome Crohn's colitis Crohn's disease Down syndrome Evans' syndrome Gaucher's disease Goodpasture syndrome Graves' disease Griscelli syndrome Guillain-Barre syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Japanese encephalitis Kawasaki disease Langerhans-cell histiocytosis Lown-Ganong-Levine syndrome Marfan syndrome Meniere's disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Takayasu's arteritis Wolff-Parkinson-White syndrome X-linked agammaglobulinemia Zika fever Zollinger-Ellison syndrome abdominal aortic aneurysm acoustic neuroma acquired immunodeficiency syndrome acute chest syndrome acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis acute pericementitis adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult lymphoma age related macular degeneration aggressive NK-cell leukemia aggressive periodontitis agnosia agranulocytosis allergic asthma allergic contact dermatitis amyotrophic lateral sclerosis anemia angioedema angiomatous meningioma ankylosing spondylitis aortic valve disease 2 aortic valve stenosis aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrial fibrillation autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autosomal dominant familial periodic fever bacterial sepsis benign meningioma bile duct adenocarcinoma bile duct carcinoma biliary atresia breast cancer breast carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiovascular system disease carotid artery thrombosis carotid stenosis cataract 32 multiple types central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood lymphoma cholangiocarcinoma chordoma chromophobe renal cell carcinoma chronic NK-cell lymphocytosis chronic kidney disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common variable immunodeficiency complement deficiency congenital hypogammaglobulinemia coronary artery disease coronary thrombosis crescentic glomerulonephritis cribriform carcinoma cryoglobulinemia cryptococcosis cystic fibrosis degeneration of macula and posterior pole dengue disease dengue hemorrhagic fever denture stomatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma distal arthrogryposis eczema herpeticum embryoma endolymphatic hydrops endometriosis of uterus endometriosis epidermodysplasia verruciformis epithelioid leiomyosarcoma epithelioid sarcoma essential thrombocythemia familial hyperlipidemia familial nephrotic syndrome fetal erythroblastosis fibrous meningioma gastritis glomerulonephritis glucose intolerance glycogen storage disease II granular cell carcinoma granulomatosis with polyangiitis head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma herpes simplex human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypersensitivity vasculitis hyperthyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma intrinsic asthma juvenile myelomonocytic leukemia kidney disease kidney failure kwashiorkor large intestine cancer leiomyosarcoma leukemia leukopenia lipoid nephrosis liver cancer liver cirrhosis lung cancer lung non-small cell carcinoma lupus erythematosus lupus nephritis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macrocytic anemia macular degeneration malaria marasmus melanoma membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia multiple myeloma multiple sclerosis myelodysplastic syndrome myeloproliferative disorder with eosinophilia myocardial infarction myxoid leiomyosarcoma nephritis nephrotic syndrome type 2 nephrotic syndrome neuroblastoma neutropenia non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsessive-compulsive disorder obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete malignant histiocytosis obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma olfactory groove meningioma oophoritis osteoarthritis pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary renal cell carcinoma parametritis parapsoriasis parasagittal meningioma paroxysmal nocturnal hemoglobinuria pelvic inflammatory disease periodontal disease periodontitis periodontosis phototoxic dermatitis pituitary adenoma pneumonia polyarteritis nodosa postinflammatory pulmonary fibrosis prediabetes syndrome progressive muscular atrophy protein-energy malnutrition psammomatous meningioma psoriasis psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis pustulosis of palm and sole pyosalpinx rapidly progressive glomerulonephritis red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease reticulosarcoma rheumatic fever rheumatoid arthritis salpingitis sarcoidosis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma scleroderma secretory meningioma severe congenital neutropenia sickle cell anemia silent myocardial infarction situs inversus skin disease skin melanoma speech-language disorder-1 spinal meningioma spindle cell sarcoma spondyloarthropathy spondylosis squamous cell carcinoma steatotic liver disease stomatitis subacute delirium systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma temporal arteritis thrombocytopenia thrombophilia thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma toxic shock syndrome transient hypogammaglobulinemia of infancy transitional meningioma tuberculosis tuberculous pneumothorax tuberous sclerosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ulcerative stomatitis uremia urticaria uveoparotid fever vascular disease vasculitis viral infectious disease yellow fever
O75019	Leukocyte immunoglobulin-like receptor subfamily A member 1	LILRA1 LIR6	6	0
O75022	Leukocyte immunoglobulin-like receptor subfamily B member 3	LILRB3 ILT5 LIR3	5	1
O75023	Leukocyte immunoglobulin-like receptor subfamily B member 5	LILRB5 LIR8	6	7
O75027	Iron-sulfur clusters transporter ABCB7, mitochondrial	ABCB7 ABC7	3	1
O75030	Microphthalmia-associated transcription factor	MITF BHLHE32	4	1
O75037	Kinesin-like protein KIF21B	KIF21B KIAA0449	1	1
O75038	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2	PLCH2 KIAA0450 PLCL4	1	1	azoospermia intellectual disability learning disability schizophrenia
O75044	SLIT-ROBO Rho GTPase-activating protein 2	SRGAP2 ARHGAP34 FNBP2 KIAA0456 SRGAP2A	5	1
O75051	Plexin-A2	PLXNA2 KIAA0463 OCT PLXN2	10	8
O75052	Carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein	NOS1AP CAPON KIAA0464	0	1
O75054	Immunoglobulin superfamily member 3	IGSF3 EWI3 KIAA0466	9	15
O75056	Syndecan-3	SDC3 KIAA0468	32	4	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 Creutzfeldt-Jakob disease Duchenne muscular dystrophy Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 breast fibrocystic disease cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis C hepatocellular carcinoma liver cancer microglandular adenosis muscular dystrophy nonpapillary renal cell carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma
O75063	Glycosaminoglycan xylosylkinase	FAM20B KIAA0475	2	4	Desbuquois dysplasia Ehlers-Danlos syndrome osteogenesis imperfecta parapsoriasis psoriasis pustulosis of palm and sole
O75064	DENN domain-containing protein 4B	DENND4B KIAA0476	0	1
O75071	EF-hand calcium-binding domain-containing protein 14	EFCAB14 KIAA0494	9	11
O75072	Ribitol-5-phosphate transferase FKTN	FKTN FCMD	1	0	Axenfeld-Rieger syndrome Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome X-linked dilated cardiomyopathy agnosia anaplastic astrocytoma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect 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 bilateral optic nerve hypoplasia blindness breast cancer buphthalmos campomelic dysplasia cancer cardiomyopathy cataract centronuclear myopathy childhood cerebral astrocytoma cleft lip cleft palate coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy congestive heart failure cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia craniosynostosis cryptorchidism developmental coordination disorder dextro-looped transposition of the great arteries dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy embryoma endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis fibrillary astrocytoma fibromyalgia fundus dystrophy gallbladder cancer gallbladder carcinoma gemistocytic astrocytoma glaucoma high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hyperopia hypertrophic cardiomyopathy hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels juvenile pilocytic astrocytoma learning disability limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy lissencephaly malignant astrocytoma mechanical strabismus megaconial type congenital muscular dystrophy megalocornea meningocele microcephaly microphthalmia multiple types of congenital heart defects 6 muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myocarditis myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myositis nemaline myopathy nonepidermolytic palmoplantar keratoderma 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 dextro-looped transposition of the great arteries 1 obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy palmoplantar keratosis patent foramen ovale peripheral retinal degeneration pilocytic astrocytoma placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 protoplasmic astrocytoma pulmonary valve stenosis recurrent corneal erosion renal agenesis retinal detachment rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stomach cancer stomach carcinoma strabismus subependymal giant cell astrocytoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type visual epilepsy
O75074	Low-density lipoprotein receptor-related protein 3	LRP3	3	0

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