GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3201 - 3225** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
P23510	Tumor necrosis factor ligand superfamily member 4	TNFSF4 TXGP1	4	0
Q8IVL8	Carboxypeptidase O	CPO	4	0	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 DiGeorge syndrome Pick's disease Reye syndrome Van der Woude syndrome cerebral degeneration colorectal cancer colorectal carcinoma craniosynostosis hereditary coproporphyria large intestine cancer melorheostosis velocardiofacial syndrome
Q9Y6X8	Zinc fingers and homeoboxes protein 2	ZHX2 AFR1 KIAA0854 RAF	4	2
Q6UWJ8	CD164 sialomucin-like 2 protein	CD164L2	4	1
Q13634	Cadherin-18	CDH18 CDH14	4	0
Q86UR5	Regulating synaptic membrane exocytosis protein 1	RIMS1 KIAA0340 RAB3IP2 RIM1	4	1
Q9UJC3	Protein Hook homolog 1	HOOK1	4	1
Q9HBT6	Cadherin-20	CDH20 CDH7L3	4	0
P78344	Eukaryotic translation initiation factor 4 gamma 2	EIF4G2 DAP5	4	3
Q9UP38	Frizzled-1	FZD1	4	3
P41221	Protein Wnt-5a	WNT5A	4	10
A0A0C4DGH0	CD276 molecule	CD276	4	0
P40939	Trifunctional enzyme subunit alpha, mitochondrial	HADHA HADH	4	4	Barth syndrome HELLP syndrome Norum disease Reye syndrome Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia acquired immunodeficiency syndrome adult respiratory distress syndrome agnosia alpha 1-antitrypsin deficiency alternating exotropia amyotrophic lateral sclerosis arthritis arthropathy blindness breast cancer bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease cholestasis choreaacanthocytosis clubfoot cone-rod dystrophy congenital adrenal hyperplasia congenital stationary night blindness 1A congenital stationary night blindness congestive heart failure coronary artery disease cystinuria cytochrome-c oxidase deficiency disease developmental coordination disorder diabetes mellitus dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism endomyocardial fibrosis epilepsy exotropia familial hypertrophic cardiomyopathy familial periodic paralysis fibromyalgia fundus albipunctatus galactosemia gallbladder disease 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 hemophagocytic lymphohistiocytosis hepatitis C human immunodeficiency virus infectious disease hypercalcemia hypertrophic cardiomyopathy hypoglycemia hypolipoproteinemia hypoparathyroidism inflammatory bowel disease inherited metabolic disorder intellectual disability lactic acidosis learning disability liver disease lung benign neoplasm lung cancer lung carcinoma metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse monocular exotropia myoglobinuria myopathy myopia myositis nephrocalcinosis neuropathy newborn respiratory distress syndrome night blindness obesity obsolete asthenopia osteoarthritis peripheral nervous system disease phosphorus metabolism disease placental insufficiency polyneuropathy pre-eclampsia progressive muscular atrophy prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinal disease retinitis pigmentosa retinitis sick sinus syndrome staphyloma posticum steatotic liver disease sudden infant death syndrome tricuspid valve insufficiency type 2 diabetes mellitus urea cycle disorder visual epilepsy von Willebrand's disease 2 von Willebrand's disease
Q92797	Symplekin	SYMPK SPK	4	1
Q6IA17	Single Ig IL-1-related receptor	SIGIRR	4	0
B5A937	Soluble MET variant 9	MET	4	0
P21917	D(4) dopamine receptor	DRD4	4	1
Q9UM22	Mammalian ependymin-related protein 1	EPDR1 MERP1 UCC1	4	2
P49767	Vascular endothelial growth factor C	VEGFC	4	3
Q9NS91	E3 ubiquitin-protein ligase RAD18	RAD18 RNF73	4	2
Q9HD20	Endoplasmic reticulum transmembrane helix translocase	ATP13A1 ATP13A KIAA1825	4	2
P29474	Nitric oxide synthase 3	NOS3	4	2
Q13421	Mesothelin	MSLN MPF	4	31	acoustic neuroma adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia angiomatous meningioma anthracosilicosis asbestosis benign meningioma benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma breast cancer bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervicitis cervix carcinoma childhood leukemia cholangiocarcinoma chronic salpingo-oophoritis clear cell meningioma colorectal cancer colorectal carcinoma cribriform carcinoma distal arthrogryposis embryoma endocervicitis endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma essential hypertension fibrous meningioma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatocellular carcinoma high grade glioma hypertension intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma kidney failure large intestine cancer liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma malignant pleural mesothelioma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma nephroblastoma obsolete Matthew-Wood syndrome olfactory groove meningioma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma psammomatous meningioma salivary gland cancer sarcomatoid carcinoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma thymic carcinoma thymoma transitional meningioma tubular adenocarcinoma uterine corpus cancer
Q6R327	Rapamycin-insensitive companion of mTOR	RICTOR KIAA1999	4	2
Q13393	Phospholipase D1	PLD1	4	2	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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acral lentiginous melanoma acute myocardial infarction adult respiratory distress syndrome allergic asthma amnestic disorder anaplastic astrocytoma arthritis arthropathy asthma atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bone osteosarcoma brain infarction breast cancer breast carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood osteosarcoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma complex partial epilepsy congestive heart failure coronary thrombosis dementia diabetes mellitus disseminated intravascular coagulation embryoma epilepsy fibrillary astrocytoma gastroenteritis gemistocytic astrocytoma gliosarcoma high grade glioma hydronephrosis ileitis ileocolitis immune system disease inguinal hernia intrinsic asthma juvenile pilocytic astrocytoma large intestine cancer malignant astrocytoma melanoma microphthalmia middle cerebral artery infarction mitral valve insufficiency mitral valve prolapse mitral valve stenosis mixed glioma multiple sclerosis myocardial infarction newborn respiratory distress syndrome nodular prostate nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome oral candidiasis osteosarcoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma patent foramen ovale pilocytic astrocytoma pneumonia postural orthostatic tachycardia syndrome primary immunodeficiency disease prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pterygium purpura fulminans relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma retrograde amnesia rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma stomach cancer stomach carcinoma subependymal giant cell astrocytoma temporal lobe epilepsy tricuspid atresia tricuspid valve insufficiency tricuspid valve prolapse type 2 diabetes mellitus urethral diverticulum visual epilepsy

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