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 **16301 - 16325** 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
Q9Y646	Carboxypeptidase Q	CPQ LCH1 PGCP	Homo sapiens (human)	5	83
Q9Y5H2	Protocadherin gamma-A11	PCDHGA11	Homo sapiens (human)	5	0
Q15517	Corneodesmosin	CDSN	Homo sapiens (human)	5	2
O14657	Torsin-1B	TOR1B DQ1	Homo sapiens (human)	5	9
Q5T200	Zinc finger CCCH domain-containing protein 13	ZC3H13 KIAA0853	Homo sapiens (human)	5	2
P28907	ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1	CD38	Homo sapiens (human)	5	24	Alexander disease 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Bloch-Sulzberger syndrome Burkitt lymphoma Cauda equina syndrome Clouston syndrome Cockayne syndrome Crohn's colitis Crohn's disease Diamond-Blackfan anemia Down syndrome Duchenne muscular dystrophy Edwards syndrome Ehlers-Danlos syndrome Evans' syndrome Ewing sarcoma Fanconi anemia Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Japanese encephalitis Klippel-Feil syndrome Langerhans-cell histiocytosis Laron syndrome Lyme disease MHC class II deficiency Menkes disease Miller-Dieker lissencephaly syndrome Norrie disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Pick's disease Reye syndrome Richter's syndrome Scheuermann's disease T-cell acute lymphoblastic leukemia Turner syndrome Weissenbacher-Zweymuller syndrome X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia X-linked spondyloepiphyseal dysplasia tarda abdominal obesity-metabolic syndrome 1 achondroplasia acquired immunodeficiency syndrome acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute megakaryocytic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis acute promyelocytic leukemia adenosarcoma adenosine deaminase deficiency adrenoleukodystrophy adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult lymphoma aggressive systemic mastocytosis allergic asthma alveolar soft part sarcoma amnestic disorder amyloidosis androgen insensitivity syndrome angioedema ankyloblepharon-ectodermal defects-cleft lip/palate syndrome ankylosing spondylitis anorexia nervosa aortic aneurysm arthritis arthropathy asthma ataxia telangiectasia attention deficit hyperactivity disorder atypical chronic myeloid leukemia, BCR-ABL1 negative autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis bacterial sepsis basal cell carcinoma benign ependymoma beta thalassemia biphasic synovial sarcoma bone cancer bone osteosarcoma brain cancer breast cancer breast carcinoma bronchiolitis bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence carcinoma cardiovascular system disease celiac disease cellular ependymoma central nervous system disease central nervous system lymphoma centronuclear myopathy cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood B-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia childhood acute myeloid leukemia childhood leukemia childhood lymphoma chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic fatigue syndrome chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cognitive disorder collecting duct carcinoma colorectal cancer colorectal carcinoma common variable immunodeficiency cone-rod dystrophy 2 cone-rod dystrophy congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypoplastic anemia 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 myopathy 1A congenital myopathy 4A congenital structural myopathy dementia dengue disease depressive disorder dermatofibrosarcoma protuberans diabetes mellitus diabetic ketoacidosis diffuse idiopathic skeletal hyperostosis diffuse large B-cell lymphoma disease of metabolism dissociative amnesia dysthymic disorder ectodermal dysplasia embryoma encephalitis encephalomyelitis enterobiasis enterocele epilepsy epithelioid malignant peripheral nerve sheath tumor esophageal cancer esophageal carcinoma essential hypertension essential thrombocythemia extramedullary plasmacytoma facial hemiatrophy familial hyperlipidemia familial periodic paralysis follicular lymphoma giant cell glioblastoma glioblastoma glomerulonephritis gonadal dysgenesis heart disease hematologic cancer hemophilia B hepatitis C hepatocellular carcinoma herpes simplex high grade glioma human immunodeficiency virus infectious disease hypertension hypogonadism hypohidrotic ectodermal dysplasia hypomelanosis of Ito immune system disease inclusion body myositis indolent systemic mastocytosis inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability intestinal schistosomiasis intrinsic asthma juvenile myelomonocytic leukemia keratitis keratoconjunctivitis kidney disease large intestine cancer larynx sarcoma learning disability leiomyoma leukemia lipoatrophic diabetes mellitus lipodystrophy liposarcoma lissencephaly liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus lupus nephritis lymphoblastic lymphoma lymphoid leukemia lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia major depressive disorder malignant peripheral nerve sheath tumor malignant pleural mesothelioma mastocytosis medulloblastoma medulloepithelioma megaconial type congenital muscular dystrophy melancholic depression melanoma microphthalmia monoclonal gammopathy of uncertain significance monoclonal paraproteinemia monophasic synovial sarcoma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multicentric Castleman disease multiple epiphyseal dysplasia multiple myeloma multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myelitis myelodysplastic syndrome myeloid leukemia myelomeningocele myofibroma myopathy myxopapillary ependymoma narcolepsy nasopharynx carcinoma nemaline myopathy nephritis nephroblastoma nervous system disease neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neurofibroma neurofibromatosis 1 neurofibromatosis neurofibrosarcoma neurogenic bladder neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete lymphoplasmacytic lymphoma obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma open-angle glaucoma optic papillitis orofaciodigital syndrome VIII osteoarthritis osteochondrodysplasia osteogenesis imperfecta type 10 osteogenesis imperfecta type 11 osteogenesis imperfecta type 12 osteogenesis imperfecta type 13 osteogenesis imperfecta type 14 osteogenesis imperfecta type 15 osteogenesis imperfecta type 16 osteogenesis imperfecta type 17 osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta type 5 osteogenesis imperfecta type 6 osteogenesis imperfecta type 7 osteogenesis imperfecta type 8 osteogenesis imperfecta type 9 osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures osteogenesis imperfecta osteoporosis osteosarcoma pancreatitis papillary adenocarcinoma papillary ependymoma papillary renal cell carcinoma papilledema parapsoriasis parasitic helminthiasis infectious disease paratyphoid fever paroxysmal nocturnal hemoglobinuria periodontitis peripheral nervous system neoplasm pigment dispersion syndrome plasma cell neoplasm plasmacytoma pleomorphic liposarcoma polycythemia vera premature menopause primary immunodeficiency disease primary open angle glaucoma primary ovarian insufficiency prolymphocytic leukemia prostate cancer prostate carcinoma proteinuria psoriasis psoriatic arthritis pure red-cell aplasia pustulosis of palm and sole refractory plasma cell neoplasm renal carcinoma renal cell carcinoma reticulosarcoma retinal edema rheumatoid arthritis rigid spine muscular dystrophy 1 sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schistosomiasis schizophrenia scoliosis severe combined immunodeficiency sick sinus syndrome sickle cell anemia skin disease skin melanoma small cell sarcoma spina bifida spinal cord disease spondylolisthesis subacute sclerosing panencephalitis substance abuse substance-related disorder supratentorial primitive neuroectodermal tumor synovial sarcoma syringomyelia systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic mastocytosis tanycytic ependymoma tethered spinal cord syndrome thalassemia thanatophoric dysplasia thyroid gland papillary carcinoma trichinosis tuberculosis 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 typhoid fever ulcerative colitis urticaria uterine fibroid uterus leiomyosarcoma vascular disease viral infectious disease visual epilepsy yellow fever
Q9Y5G5	Protocadherin gamma-A8	PCDHGA8 KIAA0327	Homo sapiens (human)	5	0
P08235	Mineralocorticoid receptor	NR3C2 MCR MLR	Homo sapiens (human)	5	1
O60502	Protein O-GlcNAcase	OGA HEXC KIAA0679 MEA5 MGEA5	Homo sapiens (human)	5	3	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 Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis tuberous sclerosis 1 tuberous sclerosis 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 visual epilepsy
Q6ZMI3	Gliomedin	GLDN COLM	Homo sapiens (human)	5	5
Q16563	Synaptophysin-like protein 1	SYPL1 SYPL	Homo sapiens (human)	5	64
Q8IUL8	Cartilage intermediate layer protein 2	CILP2	Homo sapiens (human)	5	3
Q13554	Calcium/calmodulin-dependent protein kinase type II subunit beta	CAMK2B CAM2 CAMK2 CAMKB	Homo sapiens (human)	5	1
Q9UN67	Protocadherin beta-10	PCDHB10	Homo sapiens (human)	5	1
O75899	Gamma-aminobutyric acid type B receptor subunit 2	GABBR2 GPR51 GPRC3B	Homo sapiens (human)	5	2
P22894	Neutrophil collagenase	MMP8 CLG1	Homo sapiens (human)	5	0
O60938	Keratocan	KERA SLRR2B	Homo sapiens (human)	5	3
Q15434	RNA-binding motif, single-stranded-interacting protein 2	RBMS2 SCR3	Homo sapiens (human)	5	1
P04035	3-hydroxy-3-methylglutaryl-coenzyme A reductase	HMGCR	Homo sapiens (human)	5	7
Q9P2D7	Dynein axonemal heavy chain 1	DNAH1 DHC7 DNAHC1 KIAA1410	Homo sapiens (human)	5	5
A8MVW5	HEPACAM family member 2	HEPACAM2 MIKI	Homo sapiens (human)	5	0
P56817	Beta-secretase 1	BACE1 BACE KIAA1149	Homo sapiens (human)	5	36
A1A5C7	Solute carrier family 22 member 23	SLC22A23 C6orf85	Homo sapiens (human)	5	1
Q9NZ20	Group 3 secretory phospholipase A2	PLA2G3	Homo sapiens (human)	5	3	acute myocardial infarction cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis embryoma large intestine cancer myocardial infarction silent myocardial infarction
Q6UW78	Ubiquinol-cytochrome-c reductase complex assembly factor 3	UQCC3 C11orf83	Homo sapiens (human)	5	1

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