GlyCosmos Portal

Displaying entries **13001 - 13025** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P23368	NAD-dependent malic enzyme, mitochondrial	ME2	2	1	bipolar disorder cancer embryoma epilepsy generalized epilepsy with febrile seizures plus giant cell glioblastoma glioblastoma high grade glioma idiopathic generalized epilepsy leukemia lung benign neoplasm lung cancer lung non-small cell carcinoma microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder
P26374	Rab proteins geranylgeranyltransferase component A 2	CHML REP2	1	1
O14841	5-oxoprolinase	OPLAH	1	1
Q9C0F1	Centrosomal protein of 44 kDa	CEP44 KIAA1712	4	1
Q96Q06	Perilipin-4	PLIN4 KIAA1881	1	1
P62979	Ubiquitin-ribosomal protein eS31 fusion protein	RPS27A UBA80 UBCEP1	1	1
Q99963	Endophilin-A3	SH3GL3 CNSA3 SH3D2C	1	1
Q16280	Cyclic nucleotide-gated channel alpha-2	CNGA2 CNCA CNCA1 CNCG2	1	1
Q9NV58	E3 ubiquitin-protein ligase RNF19A	RNF19A RNF19	0	1
Q00587	Cdc42 effector protein 1	CDC42EP1 BORG5 CEP1 MSE55	2	1
P50616	Protein Tob1	TOB1 TOB TROB1	2	1
P50213	Isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial	IDH3A	1	1	Zollinger-Ellison syndrome alternating hemiplegia of childhood arthritis arthropathy autonomic neuropathy bipolar disorder blindness brain disease cancer cataract central nervous system disease cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus fundus albipunctatus glaucoma hyperinsulinism hypogonadism intellectual disability keratoconus learning disability lung adenocarcinoma lung cancer nervous system disease obesity obsolete asthenopia ophthalmoplegia optic atrophy osteoarthritis pathologic nystagmus primary open angle glaucoma retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus type 2 diabetes mellitus
Q7Z3Y7	Keratin, type I cytoskeletal 28	KRT28 KRT25D	0	1
O00291	Huntingtin-interacting protein 1	HIP1	1	1
Q8N1P7	Beta/gamma crystallin domain-containing protein 2	CRYBG2 AIM1L	0	1
P49748	Very long-chain specific acyl-CoA dehydrogenase, mitochondrial	ACADVL VLCAD	3	1	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 Clouston syndrome Pearson syndrome Pick's disease Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 adrenal adenoma adrenal cortex cancer alpha 1-antitrypsin deficiency 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 atrioventricular block cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cerebral degeneration complement component 2 deficiency congenital adrenal hyperplasia dermatitis 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 endomyocardial fibrosis familial hypertrophic cardiomyopathy familial periodic paralysis gallbladder disease hemopericardium hypercalcemia hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels lactic acidosis liver disease macroglobulinemia metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency myopathy nephrocalcinosis obesity obsolete lymphoplasmacytic lymphoma patent foramen ovale pericardial effusion phosphorus metabolism disease placental insufficiency pneumonia pseudosarcomatous fibromatosis sensorineural hearing loss steatotic liver disease urea cycle disorder ventricular septal defect very long chain acyl-CoA dehydrogenase deficiency von Willebrand's disease 2 von Willebrand's disease
Q8WXA9	Splicing regulatory glutamine/lysine-rich protein 1	SREK1 SFRS12 SRRP86	0	1
Q9C019	E3 ubiquitin-protein ligase TRIM15	TRIM15 RNF93 ZNF178 ZNFB7	0	1
Q9BT73	Proteasome assembly chaperone 3	PSMG3 C7orf48 PAC3	0	1
P33076	MHC class II transactivator	CIITA MHC2TA	5	1
P55283	Cadherin-4	CDH4	9	1
Q9BSD7	Cancer-related nucleoside-triphosphatase	NTPCR C1orf57	0	1
Q9Y233	cAMP and cAMP-inhibited cGMP 3',5'-cyclic phosphodiesterase 10A	PDE10A	0	1
O43314	Inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2	PPIP5K2 HISPPD1 KIAA0433 VIP2	1	1
O15479	Melanoma-associated antigen B2	MAGEB2	0	1

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