GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (1582) Glycans (5831) Glycoproteins (18496) Lectins (298) Pathways (2090)

Displaying entries **18126 - 18150** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
P07911	Uromodulin	UMOD	17	393	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 Fabry disease IgA glomerulonephritis Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Senior-Loken syndrome Van der Woude syndrome abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute myeloid leukemia acute pancreatitis adenine phosphoribosyltransferase deficiency adult acute lymphocytic leukemia alcohol dependence alcohol use disorder anxiety disorder aortic aneurysm arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune hepatitis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease babesiosis bladder carcinoma breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia chronic interstitial cystitis chronic kidney disease chronic pyelonephritis chylomicron retention disease cleidocranial dysplasia cocaine abuse cocaine dependence congestive heart failure coronary artery disease cystic kidney disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma esophageal cancer esophageal carcinoma essential hypertension familial juvenile hyperuricemic nephropathy gallbladder disease generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance gout heart disease hepatitis A hepatitis humeroradial synostosis hypertension hyperuricemia interstitial cystitis interstitial nephritis kidney disease kidney failure leukemia lipid storage disease liver cirrhosis liver disease lupus erythematosus maple syrup urine disease middle cerebral artery infarction morphine dependence nephritis nephrolithiasis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis normal pressure hydrocephalus nutmeg liver obsolete type 1 diabetes mellitus 9 osteoporosis ovarian cancer ovarian carcinoma pancreatitis pertussis phobic disorder polycystic kidney disease 1 polycystic kidney disease 4 polydactyly prediabetes syndrome pyelitis pyelonephritis pyoureter radioulnar synostosis renal hypertension renal infectious disease secondary hyperparathyroidism systemic lupus erythematosus tuberculosis 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 uremia uric acid nephrolithiasis urinary bladder cancer urinary tract obstruction
Q9ULC0	Endomucin	EMCN EMCN2 MUC14	17	7
P17936	Insulin-like growth factor-binding protein 3	IGFBP3 IBP3	17	28
Q92576	PHD finger protein 3	PHF3 KIAA0244	17	1
Q9NR16	Scavenger receptor cysteine-rich type 1 protein M160	CD163L1 CD163B M160	17	0
O60279	Sushi domain-containing protein 5	SUSD5 KIAA0527	17	7
Q9NTG1	Polycystin family receptor for egg jelly	PKDREJ	17	0
Q13753	Laminin subunit gamma-2	LAMC2 LAMB2T LAMNB2	17	7
O00533	Neural cell adhesion molecule L1-like protein	CHL1 CALL	17	21
O15455	Toll-like receptor 3	TLR3	17	34
P98073	Enteropeptidase	TMPRSS15 ENTK PRSS7	18	1
P07942	Laminin subunit beta-1	LAMB1	18	135
Q14126	Desmoglein-2	DSG2 CDHF5	18	85
Q8WXI9	Transcriptional repressor p66-beta	GATAD2B KIAA1150	18	2
P18583	Protein SON	SON C21orf50 DBP5 KIAA1019 NREBP	18	2
Q9BYF1	Angiotensin-converting enzyme 2	ACE2	18	339
O15530	3-phosphoinositide-dependent protein kinase 1	PDPK1 PDK1	18	1
P20930	Filaggrin	FLG	18	1
O14639	Actin-binding LIM protein 1	ABLIM1 ABLIM KIAA0059 LIMAB1	18	2
P49321	Nuclear autoantigenic sperm protein	NASP	18	2
O75093	Slit homolog 1 protein	SLIT1 KIAA0813 MEGF4 SLIL1	18	2
P21333	Filamin-A	FLNA FLN FLN1	18	12
P08572	Collagen alpha-2(IV) chain	COL4A2	18	6
P14410	Sucrase-isomaltase, intestinal	SI	18	3	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 Clostridium difficile colitis Duchenne muscular dystrophy Fabry disease Gaucher's disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Japanese encephalitis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome adenocarcinoma adenoma amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 brachydactyly type C brachydactyly cancer cardiomyopathy cardiovascular system disease cerebral degeneration chronic lymphocytic leukemia chylomicron retention disease colitis colorectal cancer colorectal carcinoma congenital disorder of glycosylation congenital muscular dystrophy coronary artery disease cribriform carcinoma cystic fibrosis cystinuria dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism distal myopathy embryoma endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia gastric cardia adenocarcinoma gastroenteritis gastrointestinal system disease glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hyperglycemia hypertrophic cardiomyopathy hypoglycemia ileitis ileocolitis intestinal disease irritable bowel syndrome kwashiorkor lactose intolerance large intestine cancer limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease major depressive disorder marasmus melancholic depression muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myotonic dystrophy type 1 myotonic dystrophy type 2 nephrolithiasis neurocirculatory asthenia neurodegenerative disease nutmeg liver nutrition disease obesity 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 melancholia oculopharyngeal muscular dystrophy peptic ulcer disease prediabetes syndrome progressive muscular atrophy prolactinoma protein-energy malnutrition punctate palmoplantar keratoderma type III rippling muscle disease 2 sudden infant death syndrome tropical sprue tubular adenocarcinoma type 2 diabetes mellitus uric acid nephrolithiasis viral infectious disease yellow fever
O60469	Cell adhesion molecule DSCAM	DSCAM	18	0

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