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 **9151 - 9175** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
B5DFM7	Cation channel sperm-associated auxiliary subunit delta	Catsperd Tmem146	Rattus norvegicus (Norway rat)	7	0
Q06685	Inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase	VIP1	Saccharomyces cerevisiae S288C	7	1
P14384	Carboxypeptidase M	CPM	Homo sapiens (human)	7	36	adult liposarcoma anthracosilicosis anxiety disorder aphasia asbestosis atrial fibrillation breast cancer breast carcinoma cancer childhood liposarcoma colorectal cancer colorectal carcinoma embryoma endometriosis of ovary endometriosis generalized anxiety disorder inflammatory liposarcoma kidney failure large intestine cancer lipoma liposarcoma lung adenocarcinoma lung cancer multiple symmetric lipomatosis pleomorphic lipoma pleomorphic liposarcoma proliferative diabetic retinopathy sclerosing liposarcoma silicosis well-differentiated liposarcoma
O15014	Zinc finger protein 609	ZNF609 KIAA0295	Homo sapiens (human)	7	1
A0A8B8W3U4	Angiotensin-converting enzyme	LOC118886312 ACE	Balaenoptera musculus (blue whale)	7	0
P36941	Tumor necrosis factor receptor superfamily member 3	LTBR D12S370 TNFCR TNFR3 TNFRSF3	Homo sapiens (human)	7	3
P19440	Glutathione hydrolase 1 proenzyme	GGT1 GGT	Homo sapiens (human)	7	133	ARC syndrome Aicardi-Goutieres syndrome Alagille syndrome 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Leber hereditary optic neuropathy Pick's disease Potter's syndrome Reye syndrome Werner syndrome abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy adult acute lymphocytic leukemia alcohol dependence alcohol use disorder alcoholic liver cirrhosis allergic asthma ameloblastoma anthracosilicosis anthracosis arteriosclerotic cardiovascular disease arthritis arthrogryposis, renal dysfunction, and cholestasis 1 arthropathy asbestosis asthma atherosclerosis atrial fibrillation benign recurrent intrahepatic cholestasis bile duct adenocarcinoma bile duct carcinoma biliary atresia breast apocrine carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia cholangiocarcinoma cholecystitis cholestasis chromophobe renal cell carcinoma chronic kidney disease citrullinemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common wart coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy differentiated thyroid gland carcinoma distal arthrogryposis embryoma endometrial cancer endometrial carcinoma epithelioid leiomyosarcoma essential hypertension essential thrombocythemia exfoliation syndrome familial hyperlipidemia gallbladder cancer gallbladder carcinoma gallbladder disease gamma-glutamyl transpeptidase deficiency gelatinous drop-like corneal dystrophy gestational trophoblastic neoplasm glucose intolerance glycogen storage disease VIII granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileus inflammatory bowel disease inflammatory liposarcoma influenza intellectual disability interstitial lung disease intestinal obstruction intrahepatic cholangiocarcinoma intrahepatic cholestasis intrinsic asthma kidney failure large intestine cancer learning disability leiomyosarcoma leukemia liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma maturity-onset diabetes of the young melanoma mitochondrial metabolism disease mitochondrial myopathy morbid obesity myelodysplastic syndrome myocardial infarction myxoid leiomyosarcoma nasopharynx carcinoma neonatal jaundice nodular prostate nonpapillary renal cell carcinoma nontoxic goiter nutmeg liver obesity obsolete dyspepsia obsolete ymphosarcoma osteoarthritis osteomalacia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma peptic ulcer disease periodontitis polycystic ovary syndrome prediabetes syndrome primary biliary cholangitis progeria progressive familial intrahepatic cholestasis 1 progressive familial intrahepatic cholestasis progressive supranuclear palsy prostate cancer prostate carcinoma prostatic adenoma renal carcinoma renal cell carcinoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing liposarcoma seminoma silent myocardial infarction skin benign neoplasm skin cancer skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tauopathy testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uremia uterine corpus cancer viral infectious disease well-differentiated liposarcoma
P08326	Neuraminidase	NA	Influenza A virus (A/equine/Kentucky/1/1981(H3N8))	7	0
Q00960	Glutamate receptor ionotropic, NMDA 2B	Grin2b	Rattus norvegicus (Norway rat)	7	11
O13875	Uncharacterized Sel1-like repeat-containing protein C1B3.10c	SPAC1B3.10c	Schizosaccharomyces pombe 972h-	7	0
Q642U8	Pre-glycoprotein polyprotein GP complex	GPC	Mammarenavirus juninense	7	0
P43096	Secreted aspartic protease 7	SAP7	Candida albicans	7	0
B4QMF4	Protein cueball	cue	Drosophila simulans	7	0
A2AI20	Glutamate receptor	Grin1	Mus musculus (house mouse)	7	0
P40002	Transcriptional regulator MIT1	MIT1	Saccharomyces cerevisiae S288C	7	1
Q9WTQ2	Podocalyxin	Podxl Pclp1	Rattus norvegicus (Norway rat)	7	0
Q03600	Integrin alpha ina-1	ina-1	Caenorhabditis elegans	7	0
P16546	Spectrin alpha chain, non-erythrocytic 1	Sptan1 Spna2 Spta2	Mus musculus (house mouse)	7	7
O14514	Adhesion G protein-coupled receptor B1	ADGRB1 BAI1	Homo sapiens (human)	7	3
O54826	Protein AF-10	Mllt10 Af10	Mus musculus (house mouse)	7	1
Q16656	Nuclear respiratory factor 1	NRF1	Homo sapiens (human)	7	2
P24807	Signal transducer CD24	Cd24 Cd24a Ly-52	Mus musculus (house mouse)	7	0
Q3UR55	Sodium/potassium-transporting ATPase subunit beta	Atp1b2	Mus musculus (house mouse)	7	0
Q9M3D8	L-type lectin-domain containing receptor kinase I.3	LECRK13 AtLecRK2 SR1	Arabidopsis thaliana (thale cress)	7	0
O43426	Synaptojanin-1	SYNJ1 KIAA0910	Homo sapiens (human)	7	1	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 Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder 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 bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease 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 infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy

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