GlyCosmos Portal

Displaying entries **1126 - 1150** of **18496** in total

« First

‹ Prev

…

42

43

44

45

46

47

48

49

50

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9BS26	Endoplasmic reticulum resident protein 44	ERP44 KIAA0573 TXNDC4	9	6
Q9NY47	Voltage-dependent calcium channel subunit alpha-2/delta-2	CACNA2D2 KIAA0558	11	6	absence epilepsy agnosia alternating hemiplegia of childhood autonomic neuropathy bipolar I disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebellar ataxia cerebellar disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 21 dissociated nystagmus embryoma epilepsy hypertropia idiopathic generalized epilepsy large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maple syrup urine disease mechanical strabismus nasopharynx carcinoma nervous system disease ophthalmoplegia pathologic nystagmus primary cutaneous amyloidosis prostate cancer prostate carcinoma sensorineural hearing loss sick sinus syndrome spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability type 10
O43166	Signal-induced proliferation-associated 1-like protein 1	SIPA1L1 E6TP1 KIAA0440	14	6
Q8IWK6	Adhesion G protein-coupled receptor A3	ADGRA3 GPR125	13	6
O76082	Organic cation/carnitine transporter 2	SLC22A5 OCTN2	3	6
O00451	GDNF family receptor alpha-2	GFRA2 GDNFRB RETL2 TRNR2	6	6	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
Q58FF7	Putative heat shock protein HSP 90-beta-3	HSP90AB3P HSP90BC	4	6
Q9ULB1	Neurexin-1	NRXN1 KIAA0578	6	6
Q6UXB8	Peptidase inhibitor 16	PI16 CRISP9 PSPBP	21	6
Q8IZP9	Adhesion G-protein coupled receptor G2	ADGRG2 GPR64 HE6 TM7LN2	27	6
O43734	E3 ubiquitin ligase TRAF3IP2	TRAF3IP2 C6orf2 C6orf4 C6orf5 C6orf6	1	6
P06733	Alpha-enolase	ENO1 ENO1L1 MBPB1 MPB1	4	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 Behcet's disease Burkitt lymphoma Creutzfeldt-Jakob disease Duchenne muscular dystrophy EEC syndrome Fanconi anemia IgG4-related disease Lyme disease Pick's disease Reye syndrome Richter's syndrome acquired immunodeficiency syndrome acrodysostosis acute intermittent porphyria acute interstitial pneumonia acute myocardial infarction adenocarcinoma adenoma allergic asthma anemia anxiety disorder aphthous stomatitis arthritis arthropathy asthma atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune pancreatitis 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 bacterial infectious disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma blood coagulation disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholangiocarcinoma cholera chromophobe renal cell carcinoma chronic kidney disease chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart congenital heart disease congenital muscular dystrophy corneal disease coronary thrombosis cribriform carcinoma dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy distal arthrogryposis distal myopathy ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 embryoma endocarditis endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis esophageal cancer esophageal carcinoma essential hypertension exanthem eye disease facioscapulohumeral muscular dystrophy familial retinoblastoma fibromyalgia gastric adenocarcinoma generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemorrhoid hepatitis B hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hyperglycemia hypertension hypoglycemia idiopathic interstitial pneumonia immune system disease infective endocarditis inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal volvulus intrahepatic cholangiocarcinoma intrinsic asthma invasive ductal carcinoma keratoconus kidney disease large intestine cancer leiomyoma limb-girdle muscular dystrophy liver cancer liver carcinoma liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung squamous cell carcinoma lupus nephritis macrocytic anemia male infertility membranous glomerulonephritis microphthalmia middle cerebral artery infarction mixed glioma multiple myeloma multiple sclerosis muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma nasopharynx carcinoma nephritis nephrolithiasis nephrosis neuroblastoma nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome 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 inherited blood coagulation disease oculopharyngeal muscular dystrophy oral submucous fibrosis osteoarthritis osteoporosis pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma patent ductus arteriosus perinatal necrotizing enterocolitis periodontitis phobic disorder primary pulmonary hypertension prostate cancer prostate carcinoma pulmonary hypertension pyoureter reflex sympathetic dystrophy renal carcinoma renal cell carcinoma retinoblastoma rheumatoid arthritis rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction spondyloarthropathy spondylosis squamous cell carcinoma stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder systemic lupus erythematosus tongue squamous cell carcinoma trilateral retinoblastoma tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uric acid nephrolithiasis urinary bladder cancer uterine corpus cancer uterine fibroid vasculitis
O43897	Tolloid-like protein 1	TLL1 TLL	7	6
Q12965	Unconventional myosin-Ie	MYO1E MYO1C	2	6
P08572	Collagen alpha-2(IV) chain	COL4A2	18	6
Q9H4A9	Dipeptidase 2	DPEP2	5	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 Pick's disease Reye syndrome arteriosclerotic cardiovascular disease atherosclerosis cerebral degeneration coronary artery disease laryngeal disease ovarian cancer ovarian carcinoma tracheal disease
P49915	GMP synthase [glutamine-hydrolyzing]	GMPS	3	6
Q9NZC3	Glycerophosphodiester phosphodiesterase 1	GDE1 MIR16	3	6
P42658	Dipeptidyl aminopeptidase-like protein 6	DPP6	8	6
O95460	Matrilin-4	MATN4	3	6
Q8WUT4	Leucine-rich repeat neuronal protein 4	LRRN4 C20orf75	10	6
Q14264	Endogenous retrovirus group 3 member 1 Env polyprotein	ERV3-1 ERV3	9	6
P17858	ATP-dependent 6-phosphofructokinase, liver type	PFKL	3	6	Down syndrome Lafora disease Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis bipolar disorder coronary artery disease cystinuria dentatorubral-pallidoluysian atrophy early myoclonic encephalopathy galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma liver cancer mood disorder obsolete major affective disorder 1 obsolete major affective disorder 2 progressive myoclonus epilepsy 1A progressive myoclonus epilepsy tetralogy of Fallot ventricular septal defect
Q5VU97	VWFA and cache domain-containing protein 1	CACHD1 KIAA1573 VWCD1	5	6
O76061	Stanniocalcin-2	STC2	8	6

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements