GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	Disease Ontology
Q9Y5K2	Kallikrein-4	KLK4 EMSP1 PRSS17 PSTS	1
A0A1D3TZP6	MHC class I antigen (Fragment)	HLA-B	1
C9JX27	Autophagy-related protein 9 (Fragment)	ATG9A	1
Q8NH72	Olfactory receptor 4C6	OR4C6	1
P37287	Phosphatidylinositol N-acetylglucosaminyltransferase subunit A	PIGA	1	Barrett's esophagus Burkitt lymphoma Hirschsprung's disease Marfan syndrome Miller-Dieker lissencephaly syndrome Simpson-Golabi-Behmel syndrome type 1 Simpson-Golabi-Behmel syndrome type 2 Unverricht-Lundborg syndrome West syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency aplastic anemia 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 atypical hemolytic-uremic syndrome autoimmune disease autoimmune lymphoproliferative syndrome autosomal recessive congenital ichthyosis 4B blepharospasm blood coagulation disease bone marrow cancer brain disease cancer chondroma chromosome 17p13.1 deletion syndrome coronary thrombosis dental caries dentin caries developmental and epileptic encephalopathy 3 early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy esophagitis esophagus adenocarcinoma essential thrombocythemia extramedullary plasmacytoma fetal erythroblastosis focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth hematopoietic system disease hemoglobinuria hemolytic anemia hemolytic-uremic syndrome immune system disease inflammatory bowel disease intellectual disability learning disability lissencephaly multiple congenital anomalies-hypotonia-seizures syndrome 2 multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction obsolete congenital ichthyosiform erythroderma obsolete infantile epileptic encephalopathy paroxysmal nocturnal hemoglobinuria patent foramen ovale peptic esophagitis plasma cell neoplasm plasmacytoma polycythemia vera primary pulmonary hypertension protein C deficiency protein S deficiency pulmonary embolism sensorineural hearing loss silent myocardial infarction situs inversus thrombophilia thrombotic thrombocytopenic purpura transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis vertebrobasilar insufficiency visual epilepsy
F4YTF4	MHC class I antigen (Fragment)	HLA-B	1
Q8N8U9	BMP-binding endothelial regulator protein	BMPER KIAA1965	5
A0A3S6RFN0	MHC class I antigen	HLA-B	1
Q1RMG3	receptor protein-tyrosine kinase	MERTK	1
A0A0D9SG88	Complement factor H	CFH	1
Q9UN73	Protocadherin alpha-6	PCDHA6 CNRS2	4
E0YTP2	MHC class I antigen (Fragment)	HLA-C	1
Q06AH7	Serotransferrin	TF	4
D7NNY9	MHC class I antigen (Fragment)	HLA-C	1
A0A7T3RIS4	MHC class I antigen (Fragment)	HLA-C	1
M9ZV78	MHC class I antigen (Fragment)	HLA-C	1
Q6ZN68	Putative C-mannosyltransferase DPY19L2P2	DPY19L2P2	1
A0A2H4G073	MHC class I antigen (Fragment)	HLA-C	1
Q68GS6	receptor protein-tyrosine kinase (Fragment)	EGFR	3
A0A2H4FZ81	MHC class I antigen (Fragment)	HLA-B	1
Q9H3S3	Transmembrane protease serine 5	TMPRSS5	5
A0A075B6T6	T cell receptor alpha variable 12-2	TRAV12-2	1
L7PG38	MHC class I antigen (Fragment)	HLA-B	1
C1KBJ9	MHC class I antigen (Fragment)	HLA-C	1
Q8NGX8	Olfactory receptor 6Y1	OR6Y1 OR6Y2	2

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