GlyCosmos Portal

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GlyConnect	April 19, 2023
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Displaying entries **4051 - 4075** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	Disease Ontology
Q9Y5K2	Kallikrein-4	KLK4 EMSP1 PRSS17 PSTS	Homo sapiens (human)	1
A0A1D3TZP6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
C9JX27	Autophagy-related protein 9 (Fragment)	ATG9A	Homo sapiens (human)	1
Q8NH72	Olfactory receptor 4C6	OR4C6	Homo sapiens (human)	1
P37287	Phosphatidylinositol N-acetylglucosaminyltransferase subunit A	PIGA	Homo sapiens (human)	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	Homo sapiens (human)	1
Q8N8U9	BMP-binding endothelial regulator protein	BMPER KIAA1965	Homo sapiens (human)	5
A0A3S6RFN0	MHC class I antigen	HLA-B	Homo sapiens (human)	1
Q1RMG3	receptor protein-tyrosine kinase	MERTK	Homo sapiens (human)	1
A0A0D9SG88	Complement factor H	CFH	Homo sapiens (human)	1
Q9UN73	Protocadherin alpha-6	PCDHA6 CNRS2	Homo sapiens (human)	4
E0YTP2	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
Q06AH7	Serotransferrin	TF	Homo sapiens (human)	4
D7NNY9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
A0A7T3RIS4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
M9ZV78	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
Q6ZN68	Putative C-mannosyltransferase DPY19L2P2	DPY19L2P2	Homo sapiens (human)	1
A0A2H4G073	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
Q68GS6	receptor protein-tyrosine kinase (Fragment)	EGFR	Homo sapiens (human)	3
A0A2H4FZ81	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
Q9H3S3	Transmembrane protease serine 5	TMPRSS5	Homo sapiens (human)	5
A0A075B6T6	T cell receptor alpha variable 12-2	TRAV12-2	Homo sapiens (human)	1
L7PG38	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1
C1KBJ9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1
Q8NGX8	Olfactory receptor 6Y1	OR6Y1 OR6Y2	Homo sapiens (human)	2

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