GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **126151 - 126175** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9NUN5	Lysosomal cobalamin transport escort protein LMBD1	LMBRD1 C6orf209 NESI	Homo sapiens (human)	7	36
Q70626	Envelope glycoprotein gp160	env	Human immunodeficiency virus type 1 lw12.3 isolate	29	36
Q969P0	Immunoglobulin superfamily member 8	IGSF8 CD81P3 EWI2 KCT4	Homo sapiens (human)	4	36
P14384	Carboxypeptidase M	CPM	Homo sapiens (human)	7	36	adult liposarcoma anthracosilicosis anxiety disorder aphasia asbestosis atrial fibrillation breast cancer breast carcinoma cancer childhood liposarcoma colorectal cancer colorectal carcinoma embryoma endometriosis of ovary endometriosis generalized anxiety disorder inflammatory liposarcoma kidney failure large intestine cancer lipoma liposarcoma lung adenocarcinoma lung cancer multiple symmetric lipomatosis pleomorphic lipoma pleomorphic liposarcoma proliferative diabetic retinopathy sclerosing liposarcoma silicosis well-differentiated liposarcoma
Q07837	Amino acid transporter heavy chain SLC3A1	SLC3A1 NBAT	Homo sapiens (human)	6	37	IgA glomerulonephritis Marfan syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction 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 breast cancer breast carcinoma bulimia nervosa calcinosis calcium metabolism disease cancer chronic kidney disease colon carcinoma colorectal cancer congenital myasthenic syndrome 22 congenital ptosis coronary thrombosis cystinuria diabetes mellitus diabetic ketoacidosis distal myopathy epilepsy essential hypertension facioscapulohumeral muscular dystrophy galactosemia giant cell glioblastoma glioblastoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease high grade glioma hypercalcemia hypertension hypoglycemia hypogonadism hypotonia-cystinuria syndrome interstitial nephritis kidney failure lactic acidosis limb-girdle muscular dystrophy muscular dystrophy myocardial infarction nephrocalcinosis nephrolithiasis nephrosclerosis 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 oculopharyngeal muscular dystrophy panic disorder phosphorus metabolism disease primary pulmonary hypertension prostate cancer prostate carcinoma ptosis pyelitis pyelonephritis renal hypertension renal infectious disease silent myocardial infarction situs inversus synovial sarcoma tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis urinary tract obstruction vesicoureteral reflux visual epilepsy
Q8IV08	5'-3' exonuclease PLD3	PLD3	Homo sapiens (human)	6	37	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 Henoch-Schoenlein purpura Pick's disease Reye syndrome amyloidosis atopic dermatitis cerebral degeneration congenital nystagmus conjunctival folliculosis conjunctivitis dermatitis dissociated nystagmus hypersensitivity vasculitis keratitis keratoconjunctivitis pathologic nystagmus rheumatoid arthritis scleroderma shipyard eye spinocerebellar ataxia 46 spontaneous ocular nystagmus systemic scleroderma
P08101	Low affinity immunoglobulin gamma Fc region receptor II	Fcgr2 Fcgr2b Ly-17	Mus musculus (house mouse)	5	37
Q86SQ4	Adhesion G-protein coupled receptor G6	ADGRG6 DREG GPR126 VIGR	Homo sapiens (human)	26	37
Q9Y639	Neuroplastin	NPTN SDFR1 SDR1	Homo sapiens (human)	8	37
Q6UWY5	Olfactomedin-like protein 1	OLFML1	Homo sapiens (human)	3	37
P19022	Cadherin-2	CDH2 CDHN NCAD	Homo sapiens (human)	12	37
Q03591	Complement factor H-related protein 1	CFHR1 CFHL CFHL1 CFHL1P CFHR1P FHR1 HFL1 HFL2	Homo sapiens (human)	2	37
P49746	Thrombospondin-3	THBS3 TSP3	Homo sapiens (human)	5	38
O00391	Sulfhydryl oxidase 1	QSOX1 QSCN6	Homo sapiens (human)	28	38
P12318	Low affinity immunoglobulin gamma Fc region receptor II-a	FCGR2A CD32 FCG2 FCGR2A1 IGFR2	Homo sapiens (human)	2	38
P31994	Low affinity immunoglobulin gamma Fc region receptor II-b	FCGR2B CD32 FCG2 IGFR2	Homo sapiens (human)	4	38
P05186	Alkaline phosphatase, tissue-nonspecific isozyme	ALPL	Homo sapiens (human)	10	38	ARC syndrome Ehlers-Danlos syndrome Laron syndrome Loeffler syndrome Werner syndrome achondroplasia acoustic neuroma adult hypophosphatasia allergic asthma anemia angiomatous meningioma ankylosing spondylitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthrogryposis, renal dysfunction, and cholestasis 1 arthropathy asthma atherosclerosis autosomal recessive osteopetrosis 7 benign meningioma bone disease bone osteosarcoma breast cancer breast carcinoma calcinosis calcium metabolism disease campomelic dysplasia cancer cartilage disease cerebral convexity meningioma childhood hypophosphatasia chondrocalcinosis clear cell meningioma colitis connective tissue disease coronary artery disease craniosynostosis dental caries dentin caries depressive disorder diabetes mellitus dysthymic disorder embryoma embryonal carcinoma enophthalmos eosinophilic pneumonia epilepsy fibrous meningioma focal epilepsy gastroenteritis generalized anxiety disorder glomerulonephritis hereditary elliptocytosis hypercalcemia hyperostosis hyperphosphatemic familial tumoral calcinosis hypophosphatasia ileitis ileocolitis infantile hypophosphatasia inherited metabolic disorder intraorbital meningioma intraventricular meningioma intrinsic asthma keratosis follicularis kidney disease macrocytic anemia major depressive disorder melancholic depression meningioma meningothelial meningioma microcystic meningioma mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia musculoskeletal system disease nephritis nephrocalcinosis nephrolithiasis nephrosis neurotic disorder nutmeg liver obesity obsolete exophthalmos obsolete melancholia olfactory groove meningioma orbital disease 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 osteomalacia osteopetrosis osteoporosis osteosarcoma osteosclerosis parasagittal meningioma partial motor epilepsy phobic disorder phosphorus metabolism disease pituitary adenoma polyhydramnios progeria prostate cancer prostate carcinoma psammomatous meningioma pseudoxanthoma elasticum pulmonary eosinophilia pyoureter rickets schizophrenia 10 schizophrenia secondary hyperparathyroidism secretory meningioma spinal meningioma transitional meningioma type 2 diabetes mellitus uric acid nephrolithiasis visual epilepsy
P12314	High affinity immunoglobulin gamma Fc receptor I	FCGR1A FCG1 FCGR1 IGFR1	Homo sapiens (human)	7	38
P08236	Beta-glucuronidase	GUSB	Homo sapiens (human)	7	38	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 Clouston syndrome Crohn's colitis Crohn's disease De Quervain disease Fabry disease Laron syndrome Pick's disease Reye syndrome Richter's syndrome Sly syndrome Werner syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adrenal gland cancer alcohol dependence alcohol use disorder alternating hemiplegia of childhood arteriosclerotic cardiovascular disease arteriovenous malformation arthritis arthropathy atherosclerosis autonomic neuropathy bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system disease cerebral degeneration cholecystolithiasis choledocholithiasis cholelithiasis chondrodysplasia punctata chronic lymphocytic leukemia chronic myeloid leukemia chylomicron retention disease clubfoot colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease cystic fibrosis diabetes mellitus diabetic ketoacidosis diarrhea duodenum cancer elephantiasis embryoma endomyocardial fibrosis factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma gallbladder disease gastroenteritis gastrointestinal system disease gingival hypertrophy gingival overgrowth glycoproteinosis head and neck cancer head and neck squamous cell carcinoma heart cancer hepatitis B hepatitis C hepatitis hepatocellular carcinoma herpes simplex hydrocephalus hyperglycemia hypertrichosis hypertrophic cardiomyopathy ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intestinal disease islet cell tumor large intestine cancer learning disability lipid storage disease liver cancer liver disease lung adenocarcinoma lung cancer lung carcinoma lymphedema lysosomal storage disease microcystic adenoma mucolipidosis II alpha/beta mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myeloproliferative neoplasm nasopharynx carcinoma nephroblastoma nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus omphalocele ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma paraganglioma pheochromocytoma progeria prostate cancer prostate carcinoma proteinuria pulmonary tuberculosis recurrent corneal erosion retinal disease retinitis rheumatoid arthritis sarcomatoid carcinoma schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss shigellosis small intestine cancer stomach cancer stomach carcinoma subacute thyroiditis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis umbilical hernia urinary bladder cancer
Q96IY4	Carboxypeptidase B2	CPB2	Homo sapiens (human)	5	38
Q810U3	Neurofascin	Nfasc	Mus musculus (house mouse)	14	38
P27797	Calreticulin	CALR CRTC	Homo sapiens (human)	4	39	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 Barrett's esophagus Behcet's disease Budd-Chiari syndrome Burkitt lymphoma Chagas disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kuhnt-Junius degeneration Lyme disease Meckel syndrome Niemann-Pick disease type C1 Niemann-Pick 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 Sjogren's syndrome St. Louis encephalitis T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome Wilson disease abdominal obesity-metabolic syndrome 1 achalasia acquired von Willebrand syndrome acrodermatitis acromegaly actinic keratosis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adenosquamous carcinoma adult lymphoma adult medulloblastoma age related macular degeneration aggressive systemic mastocytosis ampulla of Vater benign neoplasm amyotrophic lateral sclerosis anaplastic astrocytoma anemia anthrax disease antiphospholipid syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation atrioventricular block autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant polycystic kidney disease bacterial infectious disease bacterial sepsis benign ependymoma benign mesothelioma bipolar disorder bladder carcinoma bone inflammation disease bone marrow cancer bone osteosarcoma breast cancer breast carcinoma bronchiectasis bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma cardiac arrest cardiac sarcoidosis cardiomyopathy cardiovascular system disease cat-scratch disease catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cavernous hemangioma cellular ependymoma central nervous system cancer central nervous system lymphoma cerebral creatine deficiency syndrome 1 cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood disintegrative disease childhood ependymoma childhood leukemia childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chorioangioma chromophobe renal cell carcinoma chronic lymphocytic leukemia chronic myeloid leukemia chronic neutrophilic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency congenital heart block congenital secretory sodium diarrhea 3 congenital secretory sodium diarrhea 8 congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cyclic hematopoiesis cystic fibrosis cystoid macular edema dedifferentiated liposarcoma degeneration of macula and posterior pole delusional disorder dental caries dentin caries depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma drug psychosis dysthymic disorder eclampsia embryoma endocarditis endometrial cancer endometrial carcinoma endomyocardial fibrosis enthesopathy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial adenomatous polyposis 1 familial adenomatous polyposis familial hypertrophic cardiomyopathy familial nephrotic syndrome fibrillary astrocytoma fibromyalgia follicular adenoma gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gemistocytic astrocytoma germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor glycogen storage disease II glycoproteinosis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease heart valve disease hemangioma hematologic cancer hematopoietic system disease hemochromatosis type 1 hemochromatosis hepatitis A hepatitis B hepatitis hepatocellular carcinoma high grade glioma histiocytoid hemangioma hyperpituitarism hypertension hyperthyroidism hypertrophic cardiomyopathy hypopharynx cancer ileitis ileocolitis immune system disease inclusion conjunctivitis indolent systemic mastocytosis inflammatory bowel disease intellectual disability intermittent claudication intrahepatic cholangiocarcinoma intramuscular hemangioma iron metabolism disease islet cell tumor juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma keratoconjunctivitis sicca kidney disease kwashiorkor large intestine cancer laryngeal disease learning disability left bundle branch hemiblock leukemia lichen disease lipoid nephrosis liposarcoma liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphangioma lymphoma macrocytic anemia macular degeneration macular retinal edema major depressive disorder malignant astrocytoma malignant mesothelioma marasmus mastocytosis medulloblastoma medullomyoblastoma megaesophagus melancholic depression melanoma melanotic medulloblastoma melioidosis microcystic adenoma microphthalmia mixed glioma mucolipidosis II alpha/beta myelodysplastic syndrome myelofibrosis myeloproliferative neoplasm myocardial infarction myxopapillary ependymoma nasopharynx carcinoma nephritis nephroblastoma nephrosis nephrotic syndrome neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurotic disorder nonpapillary renal cell carcinoma nutrition disease obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete ymphosarcoma oculocutaneous albinism type IA oculocutaneous albinism onchocerciasis oral submucous fibrosis osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancytopenia papillary adenoma papillary ependymoma papillary renal cell carcinoma papilloma paranoid schizophrenia parotitis peptic esophagitis periodontitis peripheral vascular disease piebaldism pilocytic astrocytoma pineal region germinoma placental insufficiency plasmacytoma pleomorphic liposarcoma pneumonia polycythemia vera polycythemia portal hypertension post-traumatic stress disorder pre-eclampsia primary immunodeficiency disease proctitis progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma psychotic disorder purpura pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease retinal vascular occlusion retinitis rheumatoid arthritis rosacea sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe acute respiratory syndrome sialadenitis sick sinus syndrome silent myocardial infarction skin melanoma speech disorder spinal muscular atrophy squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus systemic mastocytosis tanycytic ependymoma thrombocytosis thrombophilia thyroiditis thyrotoxicosis tongue cancer tongue squamous cell carcinoma tracheal disease transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trypanosomiasis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ureteral obstruction urinary bladder cancer uterine corpus cancer varicose veins vasculitis vertebrobasilar insufficiency viral infectious disease vitiligo
Q4LDE5	Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1	SVEP1 C9orf13 CCP22 SELOB	Homo sapiens (human)	33	39
P06276	Cholinesterase	BCHE CHE1	Homo sapiens (human)	12	39
Q9H5V8	CUB domain-containing protein 1	CDCP1 TRASK	Homo sapiens (human)	11	39

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