GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **976 - 1000** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9FPQ6	Vegetative cell wall protein gp1	GP1	Chlamydomonas reinhardtii	3	13
Q5T2D2	Trem-like transcript 2 protein	TREML2 C6orf76 TLT2	Homo sapiens (human)	1	13
B1AS29	Glutamate receptor ionotropic, kainate 3	Grik3 Glur7	Mus musculus (house mouse)	11	13
O60566	Mitotic checkpoint serine/threonine-protein kinase BUB1 beta	BUB1B BUBR1 MAD3L SSK1	Homo sapiens (human)	4	13
Q06418	Tyrosine-protein kinase receptor TYRO3	TYRO3 BYK DTK RSE SKY TIF	Homo sapiens (human)	7	13
P39087	Glutamate receptor ionotropic, kainate 2	Grik2 Glur6	Mus musculus (house mouse)	9	13
P97449	Aminopeptidase N	Anpep Lap-1 Lap1	Mus musculus (house mouse)	13	13
P05981	Serine protease hepsin	HPN TMPRSS1	Homo sapiens (human)	1	13
Q64676	2-hydroxyacylsphingosine 1-beta-galactosyltransferase	Ugt8 Cgt Ugt4 Ugt8a	Mus musculus (house mouse)	3	13
O00462	Beta-mannosidase	MANBA MANB1	Homo sapiens (human)	8	13	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy
O94905	Erlin-2	ERLIN2 C8orf2 SPFH2	Homo sapiens (human)	7	13
Q16585	Beta-sarcoglycan	SGCB	Homo sapiens (human)	4	13
P41234	ATP-binding cassette sub-family A member 2	Abca2 Abc2	Mus musculus (house mouse)	25	13
P97927	Laminin subunit alpha-4	Lama4	Mus musculus (house mouse)	19	13
Q92791	Endoplasmic reticulum protein SC65	P3H4 LEPREL4 NOL55 SC65	Homo sapiens (human)	3	13
P27701	CD82 antigen	CD82 KAI1 SAR2 ST6 TSPAN27	Homo sapiens (human)	5	13
P07093	Glia-derived nexin	SERPINE2 PI7 PN1	Homo sapiens (human)	5	12
Q96DT5	Dynein axonemal heavy chain 11	DNAH11	Homo sapiens (human)	2	12
Q8BXZ1	Protein disulfide-isomerase TMX3	Tmx3 Kiaa1830 Txndc10	Mus musculus (house mouse)	3	12
P42702	Leukemia inhibitory factor receptor	LIFR	Homo sapiens (human)	22	12
A0A0A6YX05	Sodium/potassium-transporting ATPase subunit beta (Fragment)	Atp1b1	Mus musculus (house mouse)	1	12
Q9P232	Contactin-3	CNTN3 KIAA1496 PANG	Homo sapiens (human)	13	12	ACTH-secreting pituitary adenoma Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Raynaud disease Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 allergic contact dermatitis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autistic disorder branchiootic syndrome breast cancer breast carcinoma cancer cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia chronic kidney disease colitis cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease depressive disorder diarrhea dilated cardiomyopathy 1B distal arthrogryposis dry eye syndrome dysthymic disorder embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy fibromyalgia gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis high grade glioma hypertension hypertrophic cardiomyopathy ileitis ileocolitis kidney disease long QT syndrome major depressive disorder melancholic depression morbid obesity mosaic variegated aneuploidy syndrome 1 nephritis nephrosis neurotic disorder obesity obsolete melancholia orofaciodigital syndrome I orofaciodigital syndrome X paraplegia parapsoriasis peripheral artery disease phobic disorder pituitary-dependent Cushing's disease pityriasis rubra pilaris post-traumatic stress disorder prolactinoma psoriasis pustulosis of palm and sole pyoureter restless legs syndrome spinal cord disease trichohepatoenteric syndrome 1 trichohepatoenteric syndrome xerophthalmia
O70362	Phosphatidylinositol-glycan-specific phospholipase D	Gpld1	Mus musculus (house mouse)	17	12
P70408	Cadherin-10	Cdh10	Mus musculus (house mouse)	4	12
P23576	Gamma-aminobutyric acid receptor subunit alpha-2	Gabra2 Gabra-2	Rattus norvegicus (Norway rat)	3	12

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