GlyCosmos Portal

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Displaying entries **16151 - 16175** 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
Q9NTX7	E3 ubiquitin-protein ligase RNF146	RNF146	Homo sapiens (human)	1	1
P63272	Transcription elongation factor SPT4	SUPT4H1 SPT4H SUPT4H	Homo sapiens (human)	0	1
X5D9G4	Seizure related 6-like protein 2 isoform C	SEZ6L2	Homo sapiens (human)	2	0
Q9NRM2	Zinc finger protein 277	ZNF277 NRIF4 ZNF277P	Homo sapiens (human)	1	1
A0A2U7N6S0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P17643	5,6-dihydroxyindole-2-carboxylic acid oxidase	TYRP1 CAS2 TYRP TYRRP	Homo sapiens (human)	6	0
P30566	Adenylosuccinate lyase	ADSL AMPS	Homo sapiens (human)	0	1
P07949	Proto-oncogene tyrosine-protein kinase receptor Ret	RET CDHF12 CDHR16 PTC	Homo sapiens (human)	16	4
Q9NW08	DNA-directed RNA polymerase III subunit RPC2	POLR3B	Homo sapiens (human)	1	1
Q5CAQ5	Endoplasmin	TRA1	Homo sapiens (human)	1	0
A0A0C4DGH0	CD276 molecule	CD276	Homo sapiens (human)	4	0
Q96P09	Baculoviral IAP repeat-containing protein 8	BIRC8 ILP2	Homo sapiens (human)	2	1
Q13563	Polycystin-2	PKD2 TRPP2	Homo sapiens (human)	7	10	Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome Wiskott-Aldrich syndrome acute kidney failure adrenal gland cancer atrial fibrillation atrioventricular block autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone disease breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebellar ataxia, mental retardation and dysequlibrium syndrome cholangiocarcinoma chronic kidney disease collagen disease congenital heart disease congestive heart failure connective tissue disease cystic kidney disease disorder of sexual development distal arthrogryposis duodenum cancer embryoma episodic kinesigenic dyskinesia 1 essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis focal segmental glomerulosclerosis giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gout heart cancer hermaphroditism high grade glioma hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intracranial aneurysm intrahepatic cholangiocarcinoma islet cell tumor kidney disease kidney failure laryngeal squamous cell carcinoma lung adenocarcinoma lung cancer mixed glioma nephritis nephrosis neurodegenerative disease non-congenital cyst of kidney pheochromocytoma placental insufficiency polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 4 polycystic liver disease prostate cancer prostate carcinoma pseudohermaphroditism pyoureter situs inversus small intestine cancer thoracic aortic aneurysm tuberous sclerosis uremia urinary bladder cancer
P07306	Asialoglycoprotein receptor 1	ASGR1 CLEC4H1	Homo sapiens (human)	2	0	acrodermatitis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease dermatitis hepatocellular carcinoma liver cancer nutmeg liver thrombocytopenia
P40939	Trifunctional enzyme subunit alpha, mitochondrial	HADHA HADH	Homo sapiens (human)	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
B3KNK9	Epididymis luminal protein 46	GOLPH2 HEL46	Homo sapiens (human)	2	0
P08670	Vimentin	VIM	Homo sapiens (human)	29	4
Q58I20	Sodium/potassium-transporting ATPase subunit beta-1 (Fragment)	ATP1B1	Homo sapiens (human)	1	0
O75251	NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial	NDUFS7	Homo sapiens (human)	0	1
A0A7D8V8L2	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
A0A2K4XGT4	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q9H251	Cadherin-23	CDH23 KIAA1774 KIAA1812	Homo sapiens (human)	42	4
A8MPP1	Putative ATP-dependent RNA helicase DDX11-like protein 8	DDX11L8	Homo sapiens (human)	2	1
A0A7P0TB04	Basigin	BSG	Homo sapiens (human)	3	0
F2VP82	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0

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