GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

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 **4576 - 4600** 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
O00591	Gamma-aminobutyric acid receptor subunit pi	GABRP	Homo sapiens (human)	5	0
Q9UN88	Gamma-aminobutyric acid receptor subunit theta	GABRQ	Homo sapiens (human)	1	0
P24046	Gamma-aminobutyric acid receptor subunit rho-1	GABRR1	Homo sapiens (human)	3	0
P28476	Gamma-aminobutyric acid receptor subunit rho-2	GABRR2	Homo sapiens (human)	2	0
A8MPY1	Gamma-aminobutyric acid receptor subunit rho-3	GABRR3	Homo sapiens (human)	1	0
Q8TAE8	Large ribosomal subunit protein mL64	GADD45GIP1 MRPL59 PLINP1 PRG6	Homo sapiens (human)	0	1
O14976	Cyclin-G-associated kinase	GAK DNAJC26	Homo sapiens (human)	3	4
P22466	Galanin peptides	GAL GAL1 GALN GLNN	Homo sapiens (human)	2	1
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
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
Q96A11	Galactose-3-O-sulfotransferase 3	GAL3ST3	Homo sapiens (human)	4	0
Q96RP7	Galactose-3-O-sulfotransferase 4	GAL3ST4	Homo sapiens (human)	2	1	leprosy
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
Q14376	UDP-glucose 4-epimerase	GALE	Homo sapiens (human)	0	1	Guillain-Barre syndrome Miller Fisher syndrome benign familial infantile epilepsy benign familial neonatal epilepsy benign neonatal seizures classic galactosemia cystinuria galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease stomach cancer stomach carcinoma tuberculosis
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
Q01415	N-acetylgalactosamine kinase	GALK2 GK2	Homo sapiens (human)	0	1	bronchus cancer bronchus carcinoma dental caries dentin caries lung adenocarcinoma lung cancer lung carcinoma
A0A1A7UP97	N-acetylgalactosamine-6-sulfatase	GALNS	Homo sapiens (human)	2	0
P34059	N-acetylgalactosamine-6-sulfatase	GALNS	Homo sapiens (human)	3	33	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 GM1 gangliosidosis Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Wilson disease achondroplasia acne adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma age related macular degeneration amyloidosis anthrax disease anxiety disorder arachnoiditis bacterial meningitis bacterial sepsis bacterial vaginosis bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cerebral degeneration cholangiocarcinoma chronic lymphocytic leukemia chronic obstructive pulmonary disease chronic ulcer of skin colorectal cancer colorectal carcinoma cribriform carcinoma degeneration of macula and posterior pole dental caries dentin caries diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism embryoma enterocele generalized anxiety disorder glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis hole retinal cyst impetigo influenza inguinal hernia intrahepatic cholangiocarcinoma iron metabolism disease kidney disease large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease macular degeneration macular holes mastitis meningitis metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia myositis necrotizing fasciitis nephritis osteochondrodysplasia osteoporosis pharyngitis phobic disorder prostate cancer prostate carcinoma psychotic disorder pyoderma retinal perforation rheumatic fever scarlet fever scoliosis sensorineural hearing loss stomach cancer stomach carcinoma tonsillitis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus vaginitis viral meningitis vulvitis vulvovaginitis
Q10472	Polypeptide N-acetylgalactosaminyltransferase 1	GALNT1	Homo sapiens (human)	4	5	colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure heart valve disease hepatocellular carcinoma large intestine cancer liver cancer ovarian cancer ovarian carcinoma pulmonary valve stenosis stomach cancer stomach carcinoma
Q86SR1	Polypeptide N-acetylgalactosaminyltransferase 10	GALNT10	Homo sapiens (human)	9	2	hepatitis B hepatocellular carcinoma liver cancer schizophrenia
F2Z2M7	Polypeptide N-acetylgalactosaminyltransferase 10	GALNT10	Homo sapiens (human)	1	0
B7Z5G5	Polypeptide N-acetylgalactosaminyltransferase	GALNT11	Homo sapiens (human)	1	0
Q8NCW6	Polypeptide N-acetylgalactosaminyltransferase 11	GALNT11	Homo sapiens (human)	2	5	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
A0A090N7X6	Polypeptide N-acetylgalactosaminyltransferase	GALNT11	Homo sapiens (human)	1	0
Q8IXK2	Polypeptide N-acetylgalactosaminyltransferase 12	GALNT12	Homo sapiens (human)	4	1	adenocarcinoma adenoma bilateral breast cancer cancer colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma islet cell tumor large intestine cancer microcystic adenoma papillary adenoma

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