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 **4601 - 4625** of **18496** in total

« First

‹ Prev

…

181

182

183

184

185

186

187

188

189

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
D7REL5	MHC class I polypeptide-related sequence A (Fragment)	MICA	Homo sapiens (human)	3	0
P43681	Neuronal acetylcholine receptor subunit alpha-4	CHRNA4 NACRA4	Homo sapiens (human)	3	0
A0A7D9CT54	MHC Class I chain-related protein	MICA	Homo sapiens (human)	3	0
P23219	Prostaglandin G/H synthase 1	PTGS1 COX1	Homo sapiens (human)	3	6	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 Barrett's esophagus Creutzfeldt-Jakob disease Evans' syndrome French Canadian Leigh disease Guillain-Barre syndrome Hantavirus hemorrhagic fever with renal syndrome Leigh disease Lyme disease Marfan syndrome Meckel syndrome Miller Fisher syndrome Pick's disease Reye syndrome Streptococcus pneumonia acoustic neuroma acquired immunodeficiency syndrome actinic keratosis acute chest syndrome acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma amnestic disorder amyloidosis angiomatous meningioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis autism spectrum disorder autistic disorder autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autosomal dominant polycystic kidney disease basal cell carcinoma benign meningioma bipolar disorder bladder carcinoma blood coagulation disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma bursitis cancer carcinoma cardiac arrest cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral convexity meningioma cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia childhood type dermatomyositis chorioamnionitis chromophobe renal cell carcinoma chronic ethmoiditis chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell meningioma clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cytochrome-c oxidase deficiency disease depressive disorder dermatomyositis diabetes mellitus diabetic ketoacidosis dysthymic disorder eclampsia embryoma epilepsy erythromelalgia esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue eyelid disease familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia fibrous meningioma follicular adenoma frozen shoulder gastric lymphoma gastric ulcer gastritis gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gastrointestinal system disease giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemiplegia hepatic coma hepatic encephalopathy hepatitis hepatocellular carcinoma high grade glioma histiocytosis human immunodeficiency virus infectious disease hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal disease intracranial vasospasm intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor isovaleric acidemia keratoacanthoma kidney disease kidney failure lactic acidosis large intestine cancer leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphoplasmacyte-rich meningioma major depressive disorder meconium aspiration syndrome melancholic depression melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mixed glioma mood disorder mucoepidermoid carcinoma multiple myeloma myocardial infarction myositis nephritis nephrosis neurogenic arthropathy neuromuscular disease neurotic disorder nonpapillary renal cell carcinoma nose disease nutmeg liver obesity obsolete dyspepsia obsolete inherited blood coagulation disease obsolete melancholia obstructive sleep apnea olfactory groove meningioma osteoarthritis ovarian cancer ovarian carcinoma ovarian cyst oxyphilic adenoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma peptic esophagitis peptic ulcer disease peripheral artery disease pituitary adenoma platelet-type bleeding disorder 12 pneumonia pneumothorax portal hypertension pre-eclampsia primary immunodeficiency disease primary open angle glaucoma primary pulmonary hypertension prostate cancer prostate carcinoma psammomatous meningioma psoriasis psoriatic arthritis pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renovascular hypertension retrograde amnesia rheumatoid arthritis root resorption sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia secretory meningioma silent myocardial infarction situs inversus skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal meningioma spindle cell hemangioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombosis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma tongue squamous cell carcinoma transient cerebral ischemia transitional meningioma tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia urinary bladder cancer urinary tract obstruction viral infectious disease visual epilepsy xanthomatosis
Q92791	Endoplasmic reticulum protein SC65	P3H4 LEPREL4 NOL55 SC65	Homo sapiens (human)	3	13
P98198	Phospholipid-transporting ATPase ID	ATP8B2 ATPID KIAA1137	Homo sapiens (human)	3	1
J3KS28	Angiotensin-converting enzyme (Fragment)	ACE	Homo sapiens (human)	3	0
O75362	Zinc finger protein 217	ZNF217 ZABC1	Homo sapiens (human)	3	1
Q8WVJ2	NudC domain-containing protein 2	NUDCD2	Homo sapiens (human)	3	4
O00587	Beta-1,3-N-acetylglucosaminyltransferase manic fringe	MFNG	Homo sapiens (human)	3	0
Q9P218	Collagen alpha-1(XX) chain	COL20A1 KIAA1510	Homo sapiens (human)	3	1
P01906	HLA class II histocompatibility antigen, DQ alpha 2 chain	HLA-DQA2 HLA-DXA	Homo sapiens (human)	3	0
A0A2S0BDD1	Antithrombin-III	ATIII-R2	Homo sapiens (human)	3	0
A0A286YFF7	Palmitoyl-protein thioesterase 1	PPT1	Homo sapiens (human)	3	0
P28472	Gamma-aminobutyric acid receptor subunit beta-3	GABRB3	Homo sapiens (human)	3	1
Q13490	Baculoviral IAP repeat-containing protein 2	BIRC2 API1 MIHB RNF48	Homo sapiens (human)	3	1
Q96RL7	Intermembrane lipid transfer protein VPS13A	VPS13A CHAC KIAA0986	Homo sapiens (human)	2	14
Q9ULC5	Long-chain-fatty-acid--CoA ligase 5	ACSL5 ACS5 FACL5	Homo sapiens (human)	2	2	acute chest syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma anaplastic astrocytoma basal cell carcinoma breast cancer breast carcinoma cancer carcinoma celiac disease central nervous system cancer childhood cerebral astrocytoma colorectal cancer colorectal carcinoma congestive heart failure coronary thrombosis cribriform carcinoma embryoma endometrial carcinoma essential thrombocythemia familial hyperlipidemia fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer high grade glioma juvenile pilocytic astrocytoma large intestine cancer lung benign neoplasm lung carcinoma malignant astrocytoma migraine mixed glioma myelodysplastic syndrome myocardial infarction obesity pilocytic astrocytoma protoplasmic astrocytoma sarcomatoid carcinoma sebaceous carcinoma silent myocardial infarction steatotic liver disease subependymal giant cell astrocytoma sweat gland cancer systemic lupus erythematosus tubular adenocarcinoma
Q9BUJ0	Protein ABHD14A	ABHD14A	Homo sapiens (human)	2	0
Q8NCR0	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2	Homo sapiens (human)	2	0	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia 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 bilateral optic nerve hypoplasia blindness breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder 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 obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
P0DTU4	T cell receptor beta chain MC.7.G5	TRB	Homo sapiens (human)	2	0
Q9UNI1	Chymotrypsin-like elastase family member 1	CELA1 ELA1	Homo sapiens (human)	2	0
Q9H4A4	Aminopeptidase B	RNPEP APB	Homo sapiens (human)	2	1
Q3SXY7	Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3	LRIT3	Homo sapiens (human)	2	1
A0A3B3IUC4	Alpha-galactosidase	GLA	Homo sapiens (human)	2	0

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements