GlyCosmos Portal

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Displaying entries **115401 - 115425** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	Disease Ontology
A0A0N7GBK0	Matrix protein 2	M2 M	Influenza A virus (A/South Dakota/05/2015(H3N2))	1
A0A5E4FM69	Xyloglucan endotransglucosylase/hydrolase	ALMOND_2B024313	Prunus dulcis (almond)	1
A0A3Q7U5V1	P2X purinoceptor	P2RX3	Vulpes vulpes (red fox)	1
A0A7K4SYF1	Voltage-dependent T-type calcium channel subunit alpha (Fragment)	Cacna1g	Burhinus bistriatus	1
A0A9Q0IYB7	Voltage-dependent P/Q-type calcium channel subunit alpha-1A (Fragment)	NHX12_018105	Muraenolepis orangiensis (Patagonian moray cod)	1
A0A7L4ADU2	ATS5 metalloproteinase (Fragment)	Adamts5	Circaetus pectoralis (black-chested snake-eagle)	1
A0A7L3WKT2	BACE2 secretase (Fragment)	Bace2	Atlantisia rogersi (Inaccessible Island rail)	1
I1J2W9	UDP-arabinopyranose mutase	100822188	Brachypodium distachyon (stiff brome)	1
O95528	Solute carrier family 2, facilitated glucose transporter member 10	SLC2A10 GLUT10	Homo sapiens (human)	1	Hailey-Hailey disease Legg-Calve-Perthes disease Loeys-Dietz syndrome Moyamoya disease Rothmund-Thomson syndrome X-linked dilated cardiomyopathy acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma aortic aneurysm aortic valve disease 2 aortic valve insufficiency aortic valve stenosis arterial tortuosity syndrome asthma autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB blepharophimosis bone disease breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cartilage disease cataract 32 multiple types cerebral infarction cerebrovascular disease childhood type dermatomyositis chondrosarcoma collagen disease congenital central hypoventilation syndrome congenital diaphragmatic hernia congestive heart failure connective tissue disease corneal disease coronary thrombosis craniosynostosis cribriform carcinoma cutis laxa dermatomyositis 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 endomyocardial fibrosis esophagitis essential hypertension familial hypertrophic cardiomyopathy gastroesophageal reflux disease granular cell carcinoma hiatus hernia hypertension hypertrophic cardiomyopathy hypertropia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inguinal hernia intellectual disability intermittent claudication interstitial lung disease intrinsic asthma keratoconus learning disability leukocyte adhesion deficiency 1 leukocyte adhesion deficiency lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma mal de Meleda mechanical strabismus megalocornea myocardial infarction myocarditis myopia newborn respiratory distress syndrome obstructive lung disease omphalocele ophthalmoplegia peptic esophagitis peripheral artery disease peripheral vascular disease pneumonia pulmonary emphysema pyloric stenosis respiratory failure restrictive dermopathy scoliosis silent myocardial infarction strabismus thoracic aortic aneurysm tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia vascular disease
E3Q0Y1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A7K5I8Y0	Hyaluronidase (Fragment)	Hyal1_1	Crotophaga sulcirostris (groove-billed ani)	1
Q19056	PLD phosphodiesterase domain-containing protein	CELE_E04F6.4	Caenorhabditis elegans	1
A0A7K9TRE6	Hyaluronidase (Fragment)	Hyal1_1	Chloroceryle aenea (American pygmy kingfisher)	1
A4D724	Matrix protein 2	M2 M	Influenza A virus (A/Memphis/3/1996(H1N1))	1
A0A8S0PII8	Xyloglucan endotransglucosylase/hydrolase	OLEA9_A041022	Olea europaea subsp. europaea	1
A0A7K5SRV5	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	B3gat1_0	Urocynchramus pylzowi	1
A0A060X3N1	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase	GSONMT00063637001	Oncorhynchus mykiss (rainbow trout)	1
V9I6L3	Voltage-dependent L-type calcium channel subunit alpha-1D	ACCB00046.4	Apis cerana (Asiatic honeybee)	1
A0A3B3ZC13	Hyaluronidase	HYAL2	Periophthalmus magnuspinnatus	1
Q8BJ53	UBA domain-containing protein	Ubap2l	Mus musculus (house mouse)	1
A0A2D1VZP1	Matrix protein 2	M2 M	Influenza A virus (A/Wyoming/20/2017(H3N2))	1
V5QXR8	Matrix protein 2	M2 M	Influenza A virus (A/swine/Minnesota/00401/2004(H1N1))	1
A0A8C4J9L4	Hyaluronidase	HYAL2	Dromaius novaehollandiae (emu)	1
A0A3B3ZBG4	Peptidase M12B domain-containing protein	ADAMTS5	Periophthalmus magnuspinnatus	1
V9STL9	Matrix protein 2	M2 M	Influenza A virus (A/Peru/PER176/2011(H3N2))	1

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