GlyCosmos Portal

Displaying entries **17751 - 17775** of **18496** in total

« First

‹ Prev

…

707

708

709

710

711

712

713

714

715

…

Next ›

Last »
UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q68DQ2	Very large A-kinase anchor protein	CRYBG3	6	3	bronchus cancer bronchus carcinoma cancer embryoma lung cancer lung carcinoma
Q9BW60	Very long chain fatty acid elongase 1	ELOVL1 SSC1	0	1	Cauda equina syndrome acanthosis nigricans acrodermatitis adrenoleukodystrophy cancer dermatitis dry eye syndrome hyperglycemia neurogenic bladder obsolete asthenopia xerophthalmia
Q9HB03	Very long chain fatty acid elongase 3	ELOVL3 CIG30	2	0	amnestic disorder atopic dermatitis dermatitis diabetes mellitus diabetic ketoacidosis ichthyosis prostate cancer prostate carcinoma retrograde amnesia type 2 diabetes mellitus
Q9GZR5	Very long chain fatty acid elongase 4	ELOVL4	2	6	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
Q9NYP7	Very long chain fatty acid elongase 5	ELOVL5 ELOVL2	0	1	acute myocardial infarction autosomal dominant cerebellar ataxia cancer cardiac arrest cerebellar ataxia cerebellar disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus embryoma glaucoma glomerulonephritis hyperglycemia kidney disease large intestine cancer low tension glaucoma major depressive disorder melancholic depression myocardial infarction nephritis nephrosis obesity obsolete melancholia pathologic nystagmus primary open angle glaucoma prostate cancer prostate carcinoma pyoureter retinitis pigmentosa 25 schizophrenia silent myocardial infarction spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spinocerebellar ataxia type 38 spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spontaneous ocular nystagmus steatotic liver disease type 2 diabetes mellitus
Q9H5J4	Very long chain fatty acid elongase 6	ELOVL6 FACE LCE	2	2	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
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
P98155	Very low-density lipoprotein receptor	VLDLR	8	4
B0YJ81	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1	HACD1 PTPLA	1	0	B-cell lymphoma Ehrlich tumor carcinoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Lyme disease Perry syndrome Streptococcus pneumonia T-cell acute lymphoblastic leukemia X-linked dilated cardiomyopathy achondroplasia acute biphenotypic leukemia acute leukemia agnosia allergic asthma allergic rhinitis androgen insensitivity syndrome anthrax disease aplastic anemia arrhythmogenic right ventricular cardiomyopathy asthma 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 beta thalassemia bone osteosarcoma breast adenocarcinoma breast cancer breast carcinoma cancer centronuclear myopathy cerebral infarction cerebrovascular disease cervix uteri carcinoma in situ childhood osteosarcoma clubfoot colitis common cold congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptococcosis cryptorchidism developmental coordination disorder diabetes mellitus diabetic ketoacidosis 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 distal myopathy embryoma epilepsy facioscapulohumeral muscular dystrophy gastroenteritis giant cell glioblastoma glioblastoma hepatitis B hepatitis C hepatocellular carcinoma high grade glioma ileitis ileocolitis influenza intellectual disability intrinsic asthma learning disability limb-girdle muscular dystrophy liver cancer liver cirrhosis mantle cell lymphoma megaconial type congenital muscular dystrophy multidrug-resistant tuberculosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy nemaline myopathy 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 ymphosarcoma oculopharyngeal muscular dystrophy ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma paroxysmal nocturnal hemoglobinuria pleural empyema pneumonia polycystic ovary syndrome polyhydramnios premature menopause primary ovarian insufficiency prostate cancer prostate carcinoma ptosis recurrent hypersomnia rigid spine muscular dystrophy 1 scoliosis sick sinus syndrome steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder thalassemia thymic carcinoma thymoma tuberculosis type 2 diabetes mellitus type C thymoma vasomotor rhinitis viral infectious disease wheat allergy
Q6Y1H2	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	HACD2 PTPLB	1	1
Q9P035	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 3	HACD3 BIND1 PTPLAD1	1	2	depressive disorder dysthymic disorder major depressive disorder melancholic depression neurotic disorder obsolete melancholia
Q53GQ0	Very-long-chain 3-oxoacyl-CoA reductase	HSD17B12 SDR12C1	2	2	breast cancer breast carcinoma cancer carcinoma cardiovascular system disease diabetes mellitus disease of mental health embryoma head and neck squamous cell carcinoma heart disease idiopathic scoliosis intellectual disability invasive ductal carcinoma learning disability melanoma neuroblastoma ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma psychotic disorder sarcomatoid carcinoma schizophrenia skin melanoma type 2 diabetes mellitus
Q9NZ01	Very-long-chain enoyl-CoA reductase	TECR GPSN2 SC2	2	1	Marfan syndrome agnosia autosomal recessive intellectual developmental disorder cardiovascular system disease cerebral degeneration choreatic disease depressive disorder developmental coordination disorder dyskeratosis congenita dysthymic disorder dystonia endometriosis of uterus endometriosis epilepsy focal epilepsy heart disease influenza intellectual disability learning disability lingual-facial-buccal dyskinesia major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia partial motor epilepsy pneumothorax situs inversus stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tuberous sclerosis visual epilepsy
Q12981	Vesicle transport protein SEC20	BNIP1 NIP1 SEC20L	0	1
Q8WV19	Vesicle transport protein SFT2A	SFT2D1 C6orf83	0	1
Q9UEU0	Vesicle transport through interaction with t-SNAREs homolog 1B	VTI1B VTI1 VTI1L VTI1L1 VTI2	2	1
Q15836	Vesicle-associated membrane protein 3	VAMP3 SYB3	0	1
Q9P0L0	Vesicle-associated membrane protein-associated protein A	VAPA VAP33	4	2
O95292	Vesicle-associated membrane protein-associated protein B/C	VAPB	8	1
P46459	Vesicle-fusing ATPase	NSF	0	1
O75396	Vesicle-trafficking protein SEC22b	SEC22B SEC22L1	2	5
Q16572	Vesicular acetylcholine transporter	SLC18A3 VACHT	2	0
Q9P2U8	Vesicular glutamate transporter 2	SLC17A6 DNPI VGLUT2	3	0
Q8NDX2	Vesicular glutamate transporter 3	SLC17A8 VGLUT3	1	0
Q9H598	Vesicular inhibitory amino acid transporter	SLC32A1 VGAT VIAAT	1	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements