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 **13976 - 14000** 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
P51993	4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT6	FUT6 FCT3A	Homo sapiens (human)	4	0	Kuhnt-Junius degeneration age related macular degeneration breast cancer cancer carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma degeneration of macula and posterior pole embryoma hepatocellular carcinoma large intestine cancer liver cancer macular degeneration pernicious anemia prostate cancer prostate carcinoma sarcomatoid carcinoma stomach cancer stomach carcinoma
Q11128	4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT5	FUT5	Homo sapiens (human)	4	0	bronchus cancer bronchus carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma prostate cancer prostate carcinoma stomach cancer stomach carcinoma
P22083	Alpha-(1,3)-fucosyltransferase 4	FUT4 ELFT FCT3A	Homo sapiens (human)	6	3	B-cell adult acute lymphocytic leukemia Barrett's esophagus Burkitt lymphoma Castleman disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kimura disease Leber congenital amaurosis 1 T-cell acute lymphoblastic leukemia acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adenosarcoma adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult medulloblastoma arthropathy autosomal recessive distal hereditary motor neuronopathy 1 bacterial sepsis benign mesothelioma benign peritoneal mesothelioma beta thalassemia bladder carcinoma bladder urothelial carcinoma bone marrow cancer brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy celiac disease central nervous system cancer chancroid childhood B-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia childhood leukemia childhood medulloblastoma chromophobe renal cell carcinoma chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc coronary thrombosis cribriform carcinoma cystic fibrosis embryoma embryonal carcinoma endometrial adenocarcinoma endomyocardial fibrosis esophagus squamous cell carcinoma essential thrombocythemia familial adenomatous polyposis 1 familial adenomatous polyposis familial medullary thyroid carcinoma follicular adenoma gastric ulcer gastritis gastrointestinal system cancer giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease 1 inflammatory bowel disease islet cell tumor juvenile myelomonocytic leukemia large intestine cancer laryngeal carcinoma larynx cancer leptospirosis leukemia leukocyte adhesion deficiency 2 leukocyte adhesion deficiency liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphogranuloma venereum malignant mesothelioma medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma microcystic adenoma microphthalmia mixed glioma monoclonal gammopathy of uncertain significance multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A mycosis fungoides myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction myocarditis necrotizing ulcerative gingivitis nephroblastoma neuromyelitis optica nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete leukocyte-adhesion deficiency syndrome osteoarthritis pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma paroxysmal nocturnal hemoglobinuria peptic ulcer disease peritoneal mesothelioma primary mediastinal B-cell lymphoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma septic arthritis silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma teratocarcinoma thrombosis thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma ulcerative colitis urinary bladder cancer yaws
P21217	3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase FUT3	FUT3 FT3B LE	Homo sapiens (human)	2	0	Crohn's colitis Crohn's disease achalasia adult respiratory distress syndrome alopecia anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bile duct adenocarcinoma bile duct carcinoma bipolar disorder bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma childhood leukemia childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colon adenocarcinoma colon carcinoma colorectal cancer colorectal carcinoma congenital diaphragmatic hernia coronary artery disease cystic fibrosis depressive disorder dilated cardiomyopathy 1A dilated cardiomyopathy embryoma esophagitis gastroenteritis gastroesophageal reflux disease herpes simplex hiatus hernia ileitis ileocolitis immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma invasive ductal carcinoma large intestine cancer leech infestation leukemia lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease macrocytic anemia major depressive disorder megaesophagus melancholic depression microphthalmia myiasis nonpapillary renal cell carcinoma nutmeg liver obsolete Matthew-Wood syndrome obsolete melancholia osteosarcoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis primary sclerosing cholangitis prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma rumination disorder sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing cholangitis selective IgA deficiency disease stomach cancer stomach carcinoma toxoplasmosis ulcerative colitis
Q10981	Galactoside alpha-(1,2)-fucosyltransferase 2	FUT2 SEC2	Homo sapiens (human)	3	0	Behcet's disease Crohn's colitis Crohn's disease Graves' disease Marfan syndrome acquired immunodeficiency syndrome acute pancreatitis allergic asthma anemia ankylosing spondylitis arthritis arthropathy ascending cholangitis asthma autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchiolitis bronchus cancer bronchus carcinoma cancer candidiasis cardiovascular system disease celiac disease cholangiocarcinoma cholangitis colitis colon adenocarcinoma colon carcinoma colonic disease colorectal cancer colorectal carcinoma common variable immunodeficiency cystic fibrosis dermatitis diabetes mellitus diabetic ketoacidosis diarrhea embryoma gallbladder disease gastritis gastroduodenal Crohn's disease gastroenteritis heart disease hemochromatosis type 1 hemochromatosis hepatocellular carcinoma human immunodeficiency virus infectious disease hyperthyroidism ileitis ileocolitis immune system disease immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease influenza intrahepatic cholangiocarcinoma intrinsic asthma jejunoileitis juvenile rheumatoid arthritis lactose intolerance large intestine cancer leech infestation liver cancer liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma macrocytic anemia melanoma myiasis obsolete type 1 diabetes mellitus 9 oral candidiasis osteoarthritis otitis media pancreatic cancer pancreatitis parapsoriasis pneumonia primary sclerosing cholangitis psoriasis pustulosis of palm and sole rabies sclerosing cholangitis selective IgA deficiency disease situs inversus skin melanoma status epilepticus stomach cancer stomach carcinoma sudden infant death syndrome suppurative cholangitis systemic lupus erythematosus thyrotoxicosis toxic shock syndrome toxoplasmosis tuberculosis 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 ulcerative colitis viral infectious disease
Q495W5	Alpha-(1,3)-fucosyltransferase 11	FUT11	Homo sapiens (human)	7	9	bronchus cancer bronchus carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
Q6P4F1	Alpha-(1,3)-fucosyltransferase 10	FUT10	Homo sapiens (human)	7	3	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions amnestic disorder bronchus cancer bronchus carcinoma colon adenocarcinoma dissociative amnesia frontotemporal dementia hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma retrograde amnesia
P19526	Galactoside alpha-(1,2)-fucosyltransferase 1	FUT1 H HSC	Homo sapiens (human)	2	0	B-cell lymphoma Edwards syndrome Fanconi anemia complementation group A Fanconi anemia complementation group D2 Fanconi anemia Kawasaki disease MHC class II deficiency Scheie syndrome T-cell acute lymphoblastic leukemia Wiskott-Aldrich syndrome X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 X-linked severe combined immunodeficiency acquired immunodeficiency syndrome acquired polycythemia acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adrenoleukodystrophy alcoholic hepatitis alcoholic liver cirrhosis anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome azoospermia beta thalassemia bile duct adenocarcinoma bile duct carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma 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 cerebral infarction cerebrovascular disease childhood leukemia cholangiocarcinoma chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency congenital hemolytic anemia cutaneous porphyria cystic fibrosis diarrhea distal arthrogryposis embryoma erythropoietic protoporphyria erythropoietin polycythemia essential thrombocythemia factor VIII deficiency familial erythrocytosis 2 gallbladder disease glycogen storage disease II head and neck squamous cell carcinoma hematologic cancer hematopoietic system disease hemochromatosis type 1 hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hemophagocytic lymphohistiocytosis hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease immune system disease inherited metabolic disorder intrahepatic cholangiocarcinoma juvenile myelomonocytic leukemia large intestine cancer leukemia liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma lysosomal storage disease macrocytic anemia malignant teratoma mantle cell lymphoma mature teratoma melanoma metachromatic leukodystrophy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm obsolete ymphosarcoma orofaciodigital syndrome VIII osteoarthritis ovarian cancer ovarian carcinoma pancytopenia paroxysmal nocturnal hemoglobinuria polycythemia vera polycythemia progressive muscular atrophy prostate cancer prostate carcinoma proteinuria psoriatic arthritis sarcomatoid carcinoma severe combined immunodeficiency sickle cell anemia skin benign neoplasm skin cancer skin melanoma skin squamous cell carcinoma spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma stress polycythemia teratocarcinoma teratoma tongue squamous cell carcinoma
P35637	RNA-binding protein FUS	FUS TLS	Homo sapiens (human)	13	4
P09958	Furin	FURIN FUR PACE PCSK3	Homo sapiens (human)	3	0
Q9BWH2	FUN14 domain-containing protein 2	FUNDC2 HCBP6	Homo sapiens (human)	0	1
Q9BTY2	Plasma alpha-L-fucosidase	FUCA2	Homo sapiens (human)	4	7	autoimmune disease autoimmune lymphoproliferative syndrome duodenal ulcer glycoproteinosis immune system disease schizophrenia sickle cell anemia
Q7Z6V2	alpha-L-fucosidase (Fragment)	FUCA2	Homo sapiens (human)	1	0
P04066	Tissue alpha-L-fucosidase	FUCA1	Homo sapiens (human)	5	53	Laron syndrome Sjogren's syndrome achondroplasia acquired immunodeficiency syndrome angiokeratoma anhidrosis aspartylglucosaminuria autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypothyroidism craniosynostosis critical illness polyneuropathy diabetic cataract diabetic retinopathy embryoma enterocele epilepsy fucosidosis head and neck cancer human immunodeficiency virus infectious disease hypertrichosis hypohidrosis hypothyroidism immune system disease inflammatory and toxic neuropathy intellectual disability keratoconjunctivitis sicca large intestine cancer learning disability lipoatrophic diabetes mellitus lipodystrophy livedoid vasculitis lobular neoplasia locked-in syndrome lysosomal storage disease meningoencephalitis mucoepidermoid carcinoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myxedema neuropathy papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy quadriplegia recurrent corneal erosion scoliosis sensorineural hearing loss squamous cell carcinoma syndromic X-linked intellectual disability 94 thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma vascular skin disease visual epilepsy
Q96I24	Far upstream element-binding protein 3	FUBP3 FBP3	Homo sapiens (human)	8	1
Q96AE4	Far upstream element-binding protein 1	FUBP1	Homo sapiens (human)	9	1
Q8IY81	pre-rRNA 2'-O-ribose RNA methyltransferase FTSJ3	FTSJ3	Homo sapiens (human)	2	1
Q9UET6	tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase	FTSJ1	Homo sapiens (human)	1	1
Q9C0B1	Alpha-ketoglutarate-dependent dioxygenase FTO	FTO KIAA1752	Homo sapiens (human)	2	1
P02794	Ferritin heavy chain	FTH1 FTH FTHL6	Homo sapiens (human)	3	3
E5RQL4	Formiminotransferase N-terminal subdomain-containing protein	FTCDNL1 FONG	Homo sapiens (human)	0	1
Q8N475	Follistatin-related protein 5	FSTL5 KIAA1263	Homo sapiens (human)	2	0
Q6MZW2	Follistatin-related protein 4	FSTL4 KIAA1061	Homo sapiens (human)	8	4
O95633	Follistatin-related protein 3	FSTL3 FLRG	Homo sapiens (human)	3	2
Q12841	Follistatin-related protein 1	FSTL1 FRP	Homo sapiens (human)	8	27

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