GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **118551 - 118575** of **126547** in total

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UniProt ID ▲	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NYF3	Protein FAM53C	FAM53C C5orf6	Homo sapiens (human)	1	1
Q9NYF8	Bcl-2-associated transcription factor 1	BCLAF1 BTF KIAA0164	Homo sapiens (human)	11	2
Q9NYG8	Potassium channel subfamily K member 4	KCNK4 TRAAK	Homo sapiens (human)	2	0
Q9NYJ8	TGF-beta-activated kinase 1 and MAP3K7-binding protein 2	TAB2 KIAA0733 MAP3K7IP2	Homo sapiens (human)	14	3
Q9NYK1	Toll-like receptor 7	TLR7	Homo sapiens (human)	14	3
Q9NYK5	Large ribosomal subunit protein mL39	MRPL39 C21orf92 MRPL5 RPML5	Homo sapiens (human)	0	1
Q9NYL4	Peptidyl-prolyl cis-trans isomerase FKBP11	FKBP11 FKBP19	Homo sapiens (human)	3	2
Q9NYL9	Tropomodulin-3	TMOD3	Homo sapiens (human)	1	1
Q9NYM4	G-protein coupled receptor 83	GPR83 GPR72 JP05 KIAA1540	Homo sapiens (human)	3	0
Q9NYP7	Very long chain fatty acid elongase 5	ELOVL5 ELOVL2	Homo sapiens (human)	0	1	acute myocardial infarction autosomal dominant cerebellar ataxia cancer cardiac arrest cerebellar ataxia cerebellar disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus embryoma glaucoma glomerulonephritis hyperglycemia kidney disease large intestine cancer low tension glaucoma major depressive disorder melancholic depression myocardial infarction nephritis nephrosis obesity obsolete melancholia pathologic nystagmus primary open angle glaucoma prostate cancer prostate carcinoma pyoureter retinitis pigmentosa 25 schizophrenia silent myocardial infarction spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spinocerebellar ataxia type 38 spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spontaneous ocular nystagmus steatotic liver disease type 2 diabetes mellitus
Q9NYP8	Exosomal polycystin-1-interacting protein	EPCIP C21orf120 C21orf62 CU062	Homo sapiens (human)	5	0
Q9NYP9	Protein Mis18-alpha	MIS18A C21orf45 C21orf46 FASP1	Homo sapiens (human)	2	1
Q9NYQ6	Cadherin EGF LAG seven-pass G-type receptor 1	CELSR1 CDHF9 FMI2	Homo sapiens (human)	30	46
Q9NYQ7	Cadherin EGF LAG seven-pass G-type receptor 3	CELSR3 CDHF11 EGFL1 FMI1 KIAA0812 MEGF2	Homo sapiens (human)	20	4
Q9NYQ8	Protocadherin Fat 2	FAT2 CDHF8 KIAA0811 MEGF1	Homo sapiens (human)	40	2
Q9NYU1	UDP-glucose:glycoprotein glucosyltransferase 2	UGGT2 UGCGL2 UGT2	Homo sapiens (human)	4	12	acute myocardial infarction cancer coronary thrombosis diabetes mellitus embryoma myocardial infarction silent myocardial infarction type 2 diabetes mellitus
Q9NYU2	UDP-glucose:glycoprotein glucosyltransferase 1	UGGT1 GT UGCGL1 UGGT UGT1 UGTR	Homo sapiens (human)	7	30	Crigler-Najjar syndrome Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha 1-antitrypsin deficiency beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis embryoma epilepsy gallbladder disease hepatitis C hepatitis D leukopenia liver disease neonatal jaundice neutropenia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia visual epilepsy xeroderma pigmentosum group D
Q9NYV4	Cyclin-dependent kinase 12	CDK12 CRK7 CRKRS KIAA0904	Homo sapiens (human)	16	3
Q9NYV7	Taste receptor type 2 member 16	TAS2R16	Homo sapiens (human)	2	0
Q9NYV8	Taste receptor type 2 member 14	TAS2R14	Homo sapiens (human)	3	0
Q9NYV9	Taste receptor type 2 member 13	TAS2R13	Homo sapiens (human)	2	0
Q9NYW0	Taste receptor type 2 member 10	TAS2R10	Homo sapiens (human)	2	0
Q9NYW1	Taste receptor type 2 member 9	TAS2R9	Homo sapiens (human)	1	0
Q9NYW2	Taste receptor type 2 member 8	TAS2R8	Homo sapiens (human)	1	0
Q9NYW3	Taste receptor type 2 member 7	TAS2R7	Homo sapiens (human)	2	0

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