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 **16926 - 16950** 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
P11226	Mannose-binding protein C	MBL2 COLEC1 MBL	Homo sapiens (human)	1	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 B-cell adult acute lymphocytic leukemia Balo concentric sclerosis Bannayan-Riley-Ruvalcaba syndrome Behcet's disease Burkitt lymphoma Chagas disease Clostridium difficile colitis Cowden syndrome Crohn's colitis Crohn's disease Cryptococcal meningitis Duchenne muscular dystrophy Evans' syndrome Graves' disease Guillain-Barre syndrome HELLP syndrome Henoch-Schoenlein purpura 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 Kartagener syndrome Kawasaki disease Klebsiella pneumonia Lyme disease Miller Fisher syndrome Pick's disease Plasmodium falciparum malaria Reye syndrome Richter's syndrome Sjogren's syndrome Streptococcus pneumonia Turner syndrome West Nile fever acquired immunodeficiency syndrome acrodermatitis acute interstitial pneumonia acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis acute pericementitis acute poststreptococcal glomerulonephritis acute pyelonephritis adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome age related macular degeneration aggressive periodontitis agranulocytosis allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amyloidosis anal carcinoma in situ anemia angioedema ankylosing spondylitis anodontia anogenital venereal wart anthracosilicosis anthracosis antiphospholipid syndrome antithrombin III deficiency aortic valve insufficiency arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis aspergillosis asthma atherosclerosis atopic dermatitis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis 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 bacterial infectious disease bacterial meningitis bacterial sepsis bacterial vaginosis black piedra bone inflammation disease brain ischemia breast cancer breast carcinoma bronchiectasis bronchiolitis bronchitis bronchus cancer bronchus carcinoma cancer candidiasis cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease cataract 32 multiple types celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebral malaria cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood B-cell acute lymphoblastic leukemia childhood type dermatomyositis chromosome 10q23 deletion syndrome chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic obstructive pulmonary disease coccidioidomycosis colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common cold common variable immunodeficiency common wart complement component 2 deficiency congenital hypothyroidism congenital muscular dystrophy conjunctivitis coronary aneurysm coronary artery disease coronary thrombosis cryptosporidiosis cystic fibrosis cystitis degeneration of macula and posterior pole dengue disease dengue hemorrhagic fever dental caries dentin caries dermatitis dermatomyositis dermatophytosis diabetes insipidus diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disseminated intravascular coagulation distal myopathy eclampsia embryoma encephalomyelitis endometrial cancer endometrial carcinoma endomyocardial fibrosis enterobiasis epilepsy esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy fetal erythroblastosis filariasis follicular lymphoma fungal infectious disease gallbladder disease gastroenteritis gastrointestinal tularemia gestational diabetes giardiasis gliosarcoma glomerulonephritis glucose intolerance goiter gonadal dysgenesis heart disease hemiplegia hepatitis B hepatitis C hepatitis hepatocellular carcinoma hereditary angioedema herpes simplex high grade glioma histoplasmosis human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hyperhomocysteinemia hypersensitivity vasculitis hypertension hyperthyroidism hypertrophic cardiomyopathy hypothyroidism ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease influenza intermediate coronary syndrome intestinal schistosomiasis intrinsic asthma irritable bowel syndrome juvenile polyposis syndrome juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease kidney failure large intestine cancer legionellosis leishmaniasis lepromatous leprosy leprosy leukemia leukopenia limb-girdle muscular dystrophy liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lupus nephritis lymphoblastic lymphoma lymphoma macrocytic anemia macular degeneration malaria membranous glomerulonephritis meningitis meningococcal meningitis miliary tuberculosis mixed glioma multiple myeloma multiple sclerosis muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis myxedema narcolepsy nephritis nephrosis nervous system disease neurocirculatory asthenia neurogenic arthropathy neurohypophyseal diabetes insipidus neuropathy neutropenia newborn respiratory distress syndrome non-suppurative otitis media nutmeg liver obesity 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 type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive lung disease oculopharyngeal muscular dystrophy oral candidiasis osteoporosis otitis media pancreatitis panic disorder parapsoriasis patent ductus arteriosus pemphigus vulgaris pemphigus perinatal necrotizing enterocolitis periodontal disease periodontitis periodontosis peripheral nervous system disease placental insufficiency pneumonia polymyalgia rheumatica pre-eclampsia prediabetes syndrome primary biliary cholangitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary cutaneous T-cell non-Hodgkin lymphoma primary immunodeficiency disease primary open angle glaucoma prostate cancer prostate carcinoma protein C deficiency protein S deficiency psoriasis psoriatic arthritis pulmonary tuberculosis purpura fulminans pustulosis of palm and sole pyoureter renal osteodystrophy respiratory failure rheumatic fever rheumatoid arthritis rhinitis rippling muscle disease 2 schistosomiasis selective IgA deficiency disease selective IgG deficiency disease sensorineural hearing loss severe acute respiratory syndrome severe congenital neutropenia sickle cell anemia silent myocardial infarction spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spondyloarthropathy spondylosis sporotrichosis stomach cancer stomach carcinoma sudden infant death syndrome superficial mycosis systemic lupus erythematosus systemic primary carnitine deficiency disease temporal arteritis thrombocytopenia thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyrotoxicosis tonsillitis tooth agenesis trichinosis trigonitis trypanosomiasis tuberculosis tuberculous pneumothorax 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 uremia urinary schistosomiasis urinary tract obstruction uterine cancer uterine corpus cancer vaginitis vascular disease vasculitis vasomotor rhinitis viral infectious disease viral meningitis visceral leishmaniasis visual epilepsy vitiligo vulvitis vulvovaginal candidiasis vulvovaginitis white piedra yellow fever
P16435	NADPH--cytochrome P450 reductase	POR CYPOR	Homo sapiens (human)	4	3
A0A0N7A6F6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
O94905	Erlin-2	ERLIN2 C8orf2 SPFH2	Homo sapiens (human)	7	13
P24530	Endothelin receptor type B	EDNRB ETRB	Homo sapiens (human)	1	0
P07910	Heterogeneous nuclear ribonucleoproteins C1/C2	HNRNPC HNRPC	Homo sapiens (human)	2	1
A0A7D8ZIK3	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
P30740	Leukocyte elastase inhibitor	SERPINB1 ELANH2 MNEI PI2	Homo sapiens (human)	2	3
P38919	Eukaryotic initiation factor 4A-III	EIF4A3 DDX48 KIAA0111	Homo sapiens (human)	2	1
Q8N3X1	Formin-binding protein 4	FNBP4 FBP30 KIAA1014	Homo sapiens (human)	18	2
F6KS09	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q14973	Hepatic sodium/bile acid cotransporter	SLC10A1 NTCP	Homo sapiens (human)	4	0
P55107	Growth/differentiation factor 10	GDF10 BMP3B	Homo sapiens (human)	4	0
A0A0X7YLD5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P15822	Zinc finger protein 40	HIVEP1 ZNF40	Homo sapiens (human)	51	1
Q96IZ5	RNA-binding protein 41	RBM41	Homo sapiens (human)	2	1
Q15108	Pregnancy-specific beta-1 glycoprotein (Fragment)	PSG1	Homo sapiens (human)	3	0
A0A6B9QHH3	MHC class I protein (Fragment)	HLA-C	Homo sapiens (human)	1	0
D2JYI1	TGF-beta receptor type-2	TGFBR2	Homo sapiens (human)	1	0
H6VQN8	MHC class II antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P33260	Cytochrome P450 2C18	CYP2C18	Homo sapiens (human)	0	1
Q9BZE2	tRNA pseudouridine(38/39) synthase	PUS3	Homo sapiens (human)	1	2
P49862	Kallikrein-7	KLK7 PRSS6 SCCE	Homo sapiens (human)	1	1
A0MZ66	Shootin-1	SHTN1 KIAA1598	Homo sapiens (human)	2	2
A0A0B7MGA6	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0

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