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 **14126 - 14150** 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
G3V150	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3GAT3	Homo sapiens (human)	1	0
Q29RV3	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3GAT2	Homo sapiens (human)	1	0
A0A087WXU9	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	B3GAT2	Homo sapiens (human)	1	0
Q99999	Galactosylceramide sulfotransferase	GAL3ST1 CST	Homo sapiens (human)	5	17	Behcet's disease Marfan syndrome Papillon-Lefevre disease acute myocardial infarction adenocarcinoma adenoma amyotrophic lateral sclerosis anhidrosis anterior horn cell disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy 2 cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis diabetic macular edema embryoma episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma granular cell carcinoma heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza invasive ductal carcinoma lateral sclerosis liver cancer mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 osteoarthritis papillary renal cell carcinoma progressive bulbar palsy progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction situs inversus stomach cancer stomach carcinoma substance abuse substance-related disorder tuberous sclerosis tubular adenocarcinoma 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
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
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
Q96RP7	Galactose-3-O-sulfotransferase 4	GAL3ST4	Homo sapiens (human)	2	1	leprosy
Q96A11	Galactose-3-O-sulfotransferase 3	GAL3ST3	Homo sapiens (human)	4	0
Q9H3Q3	Galactose-3-O-sulfotransferase 2	GAL3ST2 GP3ST	Homo sapiens (human)	6	0	Crohn's colitis Crohn's disease ankylosing spondylitis ascending cholangitis cholangitis inflammatory bowel disease 1 inflammatory bowel disease parapsoriasis primary sclerosing cholangitis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole sclerosing cholangitis suppurative cholangitis ulcerative colitis
P51570	Galactokinase	GALK1 GALK	Homo sapiens (human)	1	1	cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract classic galactosemia colorectal cancer colorectal carcinoma cutaneous fibrous histiocytoma cystinuria diabetic cataract disease of metabolism epidermolysis bullosa simplex localized type epidermolysis bullosa simplex galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma hidradenoma inherited metabolic disorder junctional epidermolysis bullosa non-Herlitz type junctional epidermolysis bullosa with pyloric atresia junctional epidermolysis bullosa large intestine cancer liver cancer placental insufficiency senile cataract skin papilloma skin tag syringoma
P54803	Galactocerebrosidase	GALC	Homo sapiens (human)	6	5	Evans' syndrome Fabry disease Farber lipogranulomatosis Gaucher's disease Krabbe disease Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wolman disease amblyopia autoimmune thrombocytopenic purpura bipolar disorder blindness bronchus cancer bronchus carcinoma cancer cerebellar ataxia cerebellar disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital nystagmus demyelinating disease depressive disorder disease of metabolism dissociated nystagmus dysthymic disorder embryoma epilepsy glycogen storage disease II head and neck cancer head and neck squamous cell carcinoma hydrocephalus hypertropia inflammatory bowel disease laryngeal disease late onset Parkinson's disease leukodystrophy lipid storage disease low tension glaucoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease major depressive disorder mechanical strabismus melancholic depression metachromatic leukodystrophy multiple sclerosis nasopharynx carcinoma neurodegenerative disease neurotic disorder obsolete melancholia obstructive hydrocephalus ophthalmoplegia optic atrophy osteomalacia paraplegia pathologic nystagmus placental insufficiency primary open angle glaucoma relapsing fever rickets schizophrenia senile degeneration of brain sensorineural hearing loss sphingolipidosis spontaneous ocular nystagmus squamous cell carcinoma status epilepticus strabismic amblyopia strabismus systemic lupus erythematosus tongue squamous cell carcinoma tracheal disease visual epilepsy
Q5J875	GUGU gamma form	GUGU	Homo sapiens (human)	1	0
Q14C86	GTPase-activating protein and VPS9 domain-containing protein 1	GAPVD1 GAPEX5 KIAA1521 RAP6	Homo sapiens (human)	3	1
P01111	GTPase NRas	NRAS HRAS1	Homo sapiens (human)	1	1
P01116	GTPase KRas	KRAS KRAS2 RASK2	Homo sapiens (human)	1	0
P0DJR0	GTPase IMAP family member GIMD1	GIMD1	Homo sapiens (human)	0	1
Q8ND71	GTPase IMAP family member 8	GIMAP8 IAN9 IANT	Homo sapiens (human)	0	1
Q8NHV1	GTPase IMAP family member 7	GIMAP7 IAN7	Homo sapiens (human)	1	2
P01112	GTPase HRas	HRAS HRAS1	Homo sapiens (human)	2	2
O75616	GTPase Era, mitochondrial	ERAL1 HERA	Homo sapiens (human)	0	1
Q9UIJ7	GTP:AMP phosphotransferase AK3, mitochondrial	AK3 AK3L1 AK6 AKL3L	Homo sapiens (human)	2	2
Q8IYK8	GTP-binding protein REM 2	REM2	Homo sapiens (human)	0	1
O75628	GTP-binding protein REM 1	REM1 GES REM	Homo sapiens (human)	2	1
P55042	GTP-binding protein RAD	RRAD RAD	Homo sapiens (human)	1	1
Q96HU8	GTP-binding protein Di-Ras2	DIRAS2	Homo sapiens (human)	0	1

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