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 **15376 - 15400** 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
Q6U841	Sodium-driven chloride bicarbonate exchanger	SLC4A10 NBCN2 NCBE	Homo sapiens (human)	4	3
P08246	Neutrophil elastase	ELANE ELA2	Homo sapiens (human)	4	14
P07098	Gastric triacylglycerol lipase	LIPF	Homo sapiens (human)	4	0	Wolman disease lipid storage disease lysosomal acid lipase deficiency stomach cancer stomach carcinoma
Q9BXT5	Testis-expressed protein 15	TEX15	Homo sapiens (human)	4	1
Q8N2M8	CLK4-associating serine/arginine rich protein	CLASRP SFRS16 SWAP2	Homo sapiens (human)	4	1
Q12767	Transmembrane protein 94	TMEM94 KIAA0195	Homo sapiens (human)	4	0
Q14651	Plastin-1	PLS1	Homo sapiens (human)	4	2
Q8WZ79	Deoxyribonuclease-2-beta	DNASE2B DLAD	Homo sapiens (human)	4	0
P06733	Alpha-enolase	ENO1 ENO1L1 MBPB1 MPB1	Homo sapiens (human)	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
P48145	Neuropeptides B/W receptor type 1	NPBWR1 GPR7	Homo sapiens (human)	4	1
Q15714	TSC22 domain family protein 1	TSC22D1 KIAA1994 TGFB1I4 TSC22	Homo sapiens (human)	4	2
Q7L2J0	7SK snRNA methylphosphate capping enzyme	MEPCE BCDIN3	Homo sapiens (human)	4	1
Q99856	AT-rich interactive domain-containing protein 3A	ARID3A DRIL1 DRIL3 DRX E2FBP1	Homo sapiens (human)	4	1
Q9H2U2	Inorganic pyrophosphatase 2, mitochondrial	PPA2	Homo sapiens (human)	4	2
Q9Y485	DmX-like protein 1	DMXL1 XL1	Homo sapiens (human)	4	2
Q13573	SNW domain-containing protein 1	SNW1 SKIIP SKIP	Homo sapiens (human)	4	1
P04632	Calpain small subunit 1	CAPNS1 CAPN4 CAPNS	Homo sapiens (human)	4	2
Q9HC73	Cytokine receptor-like factor 2	CRLF2 CRL2 ILXR TSLPR	Homo sapiens (human)	4	1
O60330	Protocadherin gamma-A12	PCDHGA12 CDH21 FIB3 KIAA0588	Homo sapiens (human)	4	1
Q9Y6N8	Cadherin-10	CDH10	Homo sapiens (human)	4	0
Q68DL7	Uncharacterized protein C18orf63	C18orf63	Homo sapiens (human)	4	2
Q8IU57	Interferon lambda receptor 1	IFNLR1 IL28RA LICR2	Homo sapiens (human)	4	0
P26992	Ciliary neurotrophic factor receptor subunit alpha	CNTFR	Homo sapiens (human)	4	0	acute lymphoblastic leukemia adult acute lymphocytic leukemia amyotrophic lateral sclerosis attention deficit hyperactivity disorder cancer central nervous system cancer childhood acute lymphocytic leukemia childhood acute myeloid leukemia cold-induced sweating syndrome 1 cold-induced sweating syndrome gliosarcoma high grade glioma idiopathic scoliosis mixed glioma myasthenia gravis progressive muscular atrophy rheumatoid arthritis
Q9NZS2	Killer cell lectin-like receptor subfamily F member 1	KLRF1 CLEC5C ML	Homo sapiens (human)	4	0
P27105	Stomatin	STOM BND7 EPB72	Homo sapiens (human)	4	4

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