GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	Disease Ontology
Q9H6Y7	E3 ubiquitin-protein ligase RNF167	RNF167 RING105	2
A0A0A7C8M9	MHC class I antigen (Fragment)	HLA-C	1
P11150	Hepatic triacylglycerol lipase	LIPC HTGL	4	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 Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kuhnt-Junius degeneration Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation bacterial sepsis cancer cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis embryoma endometriosis of uterus endometriosis essential hypertension familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis glucose intolerance glycogen storage disease II heart disease hepatitis hyperalphalipoproteinemia 1 hyperinsulinism hypertension hypothyroidism idiopathic scoliosis intermittent claudication ischemia kidney disease large intestine cancer lipid metabolism disorder lipoid nephrosis lung cancer lung non-small cell carcinoma macroglobulinemia macular degeneration marasmus myocardial infarction myxedema nephritis nephrosis nephrotic syndrome neurodegenerative disease nutmeg liver obesity obsolete lymphoplasmacytic lymphoma obsolete type 1 diabetes mellitus 9 peripheral artery disease peripheral vascular disease pre-eclampsia prediabetes syndrome protein-energy malnutrition pyoureter schizophrenia silent myocardial infarction type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus vascular disease
A0A7P0T9V3	Activating transcription factor 6	ATF6	1
A0A1X9I454	MHC class I antigen (Fragment)	HLA-C	1
Q6IFN5	Olfactory receptor 7E24	OR7E24 OR7E24P	1
U3KPV4	Alpha-1,3-galactosyltransferase 2	A3GALT2 A3GALT2P IGBS3S	2
Q96T34	Fibroblast growth factor receptor 3 (Fragment)	FGFR3	1
A0A3B3ISQ1	ADAM metallopeptidase domain 17 (Fragment)	ADAM17	1
B4DTD8	Glypican-3	GPC3	3
E9PS32	Sortilin related receptor 1	SORL1	2
A0A1C8DVK2	MHC class I antigen (Fragment)	HLA-C	1
P02766	Transthyretin	TTR PALB	1
A0A024RBC5	Glucosamine (N-acetyl)-6-sulfatase (Sanfilippo disease IIID), isoform CRA_a (Fragment)	GNS	5
Q8WUX1	Sodium-coupled neutral amino acid transporter 5	SLC38A5 JM24 SN2 SNAT5	1
A0A0A1TTQ0	Lutheran blood group glycoprotein (Fragment)	LU	3
Q7Z7B1	Phosphatidylinositol-glycan biosynthesis class W protein	PIGW	1	Cogan syndrome Hirschsprung's disease Unverricht-Lundborg syndrome West syndrome alternating hemiplegia of childhood autonomic neuropathy blepharospasm capillary disease central nervous system disease congenital diaphragmatic hernia craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia intellectual disability learning disability monocular esotropia nervous system disease obsolete infantile epileptic encephalopathy oligohydramnios pneumonia scoliosis syndromic X-linked intellectual disability 94 telangiectasis visual epilepsy
D5FZK5	MHC class I antigen (Fragment)	HLA-B	1
Q86XR5	Proline-rich membrane anchor 1	PRIMA1	1
M9PA31	MHC class I antigen (Fragment)	HLA-C	1
D7NNX0	MHC class I antigen (Fragment)	HLA-C	1
Q8NA29	Sodium-dependent lysophosphatidylcholine symporter 1	MFSD2A MFSD2 NLS1	2
D5L9B9	MHC class I antigen (Fragment)	HLA-B	1
M9P9D8	MHC class I antigen (Fragment)	HLA-C	1
D7NP25	MHC class I antigen (Fragment)	HLA-C	1

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