GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
O00165	HCLS1-associated protein X-1	HAX1 HS1BP1	1	1
I3QHS1	MHC class I antigen (Fragment)	HLA-B	1	0
Q9NS89	Voltage-dependent P/Q-type calcium channel subunit alpha (Fragment)	CACNA1A	1	0
C9J1V2	Semaphorin 3F (Fragment)	SEMA3F	1	0
A0A1G4HPP9	MHC class I antigen (Fragment)	HLA-C	1	0
Q8NHV1	GTPase IMAP family member 7	GIMAP7 IAN7	1	2
Q05048	Cleavage stimulation factor subunit 1	CSTF1	1	2
Q9H112	Cystatin-11	CST11 CST8L	1	0
A0A6B7FVF4	MHC class I antigen	HLA-C	1	0
P51858	Hepatoma-derived growth factor	HDGF HMG1L2	1	1
A0A024R374	Cathepsin B	CTSB	1	0
Q93050	V-type proton ATPase 116 kDa subunit a 1	ATP6V0A1 ATP6N1 ATP6N1A VPP1	1	4
A0A141AZB8	MHC class I antigen (Fragment)	HLA-C	1	0
P01222	Thyrotropin subunit beta	TSHB	1	7
Q9BSL1	Ubiquitin-associated domain-containing protein 1	UBAC1 GBDR1 KPC2 UBADC1	1	2
A0A4P2ST92	MHC class I antigen	HLA-C	1	0
A0A7I2V6B0	NODAL modulator 3	NOMO3	1	0
A0A2X0SR84	MHC class I antigen	HLA-B	1	0
A3KFI2	NBL1, DAN family BMP antagonist (Fragment)	NBL1	1	0
Q8TDV2	Probable G-protein coupled receptor 148	GPR148 BTR PGR6	1	0
O95528	Solute carrier family 2, facilitated glucose transporter member 10	SLC2A10 GLUT10	1	0	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	1	0
Q15415	RNA-binding motif protein, Y chromosome, family 1 member F/J	RBMY1F RBMY1J YRRM2	1	1
Q9BVA1	Tubulin beta-2B chain	TUBB2B	1	1
A0A5F9ZHF5	Biotinidase	BTD	1	0

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