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 **1076 - 1100** 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
P20916	Myelin-associated glycoprotein	MAG GMA	Homo sapiens (human)	9	2	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 Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease type 5 Charcot-Marie-Tooth disease Guillain-Barre syndrome Kearns-Sayre syndrome Lewy body dementia MASA syndrome Marfan syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pelizaeus-Merzbacher disease Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome acute myocardial infarction adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood amyloidosis angioma serpiginosum arteriosclerotic cardiovascular disease astigmatism atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy brain stem infarction cancer capillary hemangioma cavernous hemangioma central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chorioangioma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy compartment syndrome congenital diarrhea 5 with tufting enteropathy congenital nystagmus coronary artery disease coronary thrombosis critical illness polyneuropathy demyelinating disease demyelinating polyneuropathy depressive disorder disease of mental health dissociated nystagmus dysthymic disorder embryoma familial multiple nevi flammei gliosarcoma glomus tumor hemangioma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia high grade glioma histiocytoid hemangioma hyperopia immune system disease inflammatory and toxic neuropathy intellectual disability intramuscular hemangioma learning disability lesion of sciatic nerve leukodystrophy lymphangioma major depressive disorder melancholic depression melanoma meningoencephalitis middle cerebral artery infarction mixed glioma monoclonal gammopathy of uncertain significance monoclonal paraproteinemia motor peripheral neuropathy multiple sclerosis myocardial infarction nerve compression syndrome nervous system disease neuroblastoma neuromuscular disease neuropathy neurotic disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia optic atrophy optic neuritis pancreatic cancer paraplegia pathologic nystagmus peripheral nervous system disease placental insufficiency plasma cell neoplasm poikiloderma with neutropenia polyneuropathy polyradiculoneuropathy prostate cancer prostate carcinoma psychotic disorder schizophrenia sciatic neuropathy secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma spontaneous ocular nystagmus substance abuse substance-related disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis
Q9BY15	Adhesion G protein-coupled receptor E3	ADGRE3 EMR3	Homo sapiens (human)	9	0
Q9H2C0	Gigaxonin	GAN GAN1 KLHL16	Homo sapiens (human)	9	1
P16144	Integrin beta-4	ITGB4	Homo sapiens (human)	9	18
Q7RTX0	Taste receptor type 1 member 3	TAS1R3 T1R3 TR3	Homo sapiens (human)	9	4
Q13349	Integrin alpha-D	ITGAD	Homo sapiens (human)	9	0
Q8N8S7	Protein enabled homolog	ENAH MENA	Homo sapiens (human)	9	4
Q7Z3D4	LysM and putative peptidoglycan-binding domain-containing protein 3	LYSMD3	Homo sapiens (human)	9	2
Q96NZ9	Proline-rich acidic protein 1	PRAP1 UPA	Homo sapiens (human)	9	2
Q5QP82	DDB1- and CUL4-associated factor 10	DCAF10 WDR32	Homo sapiens (human)	9	1
Q13485	Mothers against decapentaplegic homolog 4	SMAD4 DPC4 MADH4	Homo sapiens (human)	9	1
Q9NPH3	Interleukin-1 receptor accessory protein	IL1RAP C3orf13 IL1R3	Homo sapiens (human)	9	20	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 Kawasaki disease Pick's disease Reye syndrome X-linked adrenal hypoplasia congenita acute monocytic leukemia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis autism spectrum disorder autistic disorder bacterial infectious disease cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma chronic myeloid leukemia chronic obstructive pulmonary disease ciliary body disease colitis coronary artery disease endometriosis of uterus endometriosis gallbladder disease gastroenteritis head and neck squamous cell carcinoma hepatocellular carcinoma ileitis ileocolitis intellectual disability iris disease learning disability liver cancer liver disease obesity pancreatic adenocarcinoma panuveitis parapsoriasis premenstrual tension psoriasis pustulosis of palm and sole rheumatoid arthritis scleroderma skin disease systemic lupus erythematosus systemic scleroderma uveitis
C0JYY2	Apolipoprotein B (Including Ag(X) antigen)	APOB	Homo sapiens (human)	9	0
O94910	Adhesion G protein-coupled receptor L1	ADGRL1 KIAA0821 LEC2 LPHN1	Homo sapiens (human)	9	4
Q9UMS5	Protein PHTF1	PHTF1 PHTF	Homo sapiens (human)	9	2
P55283	Cadherin-4	CDH4	Homo sapiens (human)	9	1
Q15365	Poly(rC)-binding protein 1	PCBP1	Homo sapiens (human)	9	4
Q9UGM5	Fetuin-B	FETUB	Homo sapiens (human)	9	33
Q9HCM2	Plexin-A4	PLXNA4 KIAA1550 PLXNA4A PLXNA4B	Homo sapiens (human)	9	5
Q9H3R2	Mucin-13	MUC13 DRCC1 RECC	Homo sapiens (human)	9	1
Q00839	Heterogeneous nuclear ribonucleoprotein U	HNRNPU C1orf199 HNRPU SAFA U21.1	Homo sapiens (human)	9	3
Q6W4X9	Mucin-6	MUC6	Homo sapiens (human)	9	10
P49454	Centromere protein F	CENPF	Homo sapiens (human)	9	4
Q13478	Interleukin-18 receptor 1	IL18R1 IL1RRP	Homo sapiens (human)	9	2	Burkitt lymphoma CD40 ligand deficiency Clostridium difficile colitis Crohn's colitis Crohn's disease Graves' disease HELLP syndrome Holt-Oram syndrome Klippel-Trenaunay syndrome MHC class II deficiency Muckle-Wells syndrome Nezelof syndrome Norum disease Richter's syndrome Rubinstein-Taybi syndrome Sezary's disease Sjogren's syndrome T-cell acute lymphoblastic leukemia Tangier disease VACTERL association X-linked severe combined immunodeficiency abdominal aortic aneurysm abetalipoproteinemia acoustic neuroma acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenosine deaminase deficiency adult acute lymphocytic leukemia aggressive NK-cell leukemia alcohol dependence alcohol use disorder alcoholic hepatitis allergic asthma allergic disease allergic rhinitis amyotrophic lateral sclerosis angiomatous meningioma ankylosing spondylitis anthracosilicosis anthracosis arrhythmogenic right ventricular cardiomyopathy arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis ascending cholangitis asthma atherosclerosis atopic dermatitis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant familial periodic fever bacterial infectious disease benign ependymoma benign meningioma bipolar disorder bladder carcinoma bone marrow cancer bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma brucellosis cancer cardiovascular system disease cavernous hemangioma celiac disease cellular ependymoma central nervous system cancer cerebral convexity meningioma cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma childhood acute lymphocytic leukemia childhood leukemia childhood osteosarcoma cholangitis choreaacanthocytosis chorioangioma chromophobe renal cell carcinoma chronic eosinophilic leukemia chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency common variable immunodeficiency complement deficiency contagious pustular dermatitis coronary artery disease coronary thrombosis cowpox depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy dysentery eclampsia embryoma endocrine exophthalmos endometriosis of uterus endometriosis eosinophilic esophagitis erythema infectiosum esophageal cancer esophageal carcinoma esophagitis essential thrombocythemia exanthema subitum fibrous meningioma gastritis gastroenteritis gastroesophageal reflux disease giant cell glioblastoma glioblastoma gliosarcoma glomus tumor goiter head and neck squamous cell carcinoma heart disease hemangioma hematopoietic system disease hepatitis B hepatocellular carcinoma high grade glioma histiocytoid hemangioma hypereosinophilic syndrome hyperthyroidism hypolipoproteinemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intermediate coronary syndrome interstitial nephritis intestinal infectious disease intramuscular hemangioma intraorbital meningioma intraventricular meningioma intrinsic asthma irritable bowel syndrome juvenile myelomonocytic leukemia keratoconjunctivitis sicca large intestine cancer leech infestation leiomyoma leprosy leukemia liver cancer luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphangioma lymphoblastic lymphoma lymphoid leukemia lymphoplasmacyte-rich meningioma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malaria maturity-onset diabetes of the young measles melanoma meningioma meningothelial meningioma microcystic meningioma microphthalmia with limb anomalies milker's nodule mixed glioma multiple sclerosis mumps myasthenia gravis myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myiasis myocardial infarction myofibroma myotonic dystrophy type 2 myxopapillary ependymoma nail-patella syndrome neuroblastoma neurocirculatory asthenia nonpapillary renal cell carcinoma obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea olfactory groove meningioma ophthalmia neonatorum ornithosis osteoarthritis osteomyelitis osteosarcoma pancreatic cancer pancreatic carcinoma papillary ependymoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma peptic esophagitis periodontal disease periodontitis pituitary adenoma plasmacytoma polycythemia vera polycythemia pre-eclampsia primary biliary cholangitis primary cutaneous amyloidosis primary immunodeficiency disease primary pulmonary hypertension primary sclerosing cholangitis progressive muscular atrophy psammomatous meningioma psoriasis pulmonary emphysema pulpitis pustulosis of palm and sole pyelitis pyelonephritis red-green color blindness renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease rheumatoid arthritis rubella sarcoidosis sarcomatoid renal cell carcinoma schizophrenia sclerosing cholangitis secretory meningioma seminoma severe acute respiratory syndrome severe combined immunodeficiency silent myocardial infarction skin melanoma smallpox spinal meningioma split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma suppurative cholangitis systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus tanycytic ependymoma testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia-absent radius syndrome thyroid gland anaplastic carcinoma thyroid gland disease thyrotoxicosis toxoplasmosis trachoma transitional meningioma 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 ulcerative colitis urinary bladder cancer uterine fibroid uveoparotid fever variola major variola minor vasomotor rhinitis
A0A0A0MSN4	Angiotensin-converting enzyme	ACE	Homo sapiens (human)	9	0

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