GlyCosmos Portal

Displaying entries **17001 - 17025** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9NY99	Gamma-2-syntrophin	SNTG2	1	2
Q9NYA4	Myotubularin-related protein 4	MTMR4 KIAA0647 ZFYVE11	1	1	anterior horn cell disease benign mesothelioma herpes simplex malignant mesothelioma muscular atrophy
Q9NYB0	Telomeric repeat-binding factor 2-interacting protein 1	TERF2IP DRIP5 RAP1	2	1
Q9NYB5	Solute carrier organic anion transporter family member 1C1	SLCO1C1 OATP14 OATP1C1 OATPF SLC21A14	5	1
Q9NYB9	Abl interactor 2	ABI2 ARGBPIA	5	1
Q9NYC9	Dynein axonemal heavy chain 9	DNAH9 DNAH17L DNEL1 KIAA0357	1	1
Q9NYD6	Homeobox protein Hox-C10	HOXC10 HOX3I	3	1
Q9NYF0	Dapper homolog 1	DACT1 DPR1 HNG3	1	1
Q9NYF3	Protein FAM53C	FAM53C C5orf6	1	1
Q9NYF8	Bcl-2-associated transcription factor 1	BCLAF1 BTF KIAA0164	11	2
Q9NYG8	Potassium channel subfamily K member 4	KCNK4 TRAAK	2	0
Q9NYJ8	TGF-beta-activated kinase 1 and MAP3K7-binding protein 2	TAB2 KIAA0733 MAP3K7IP2	14	3
Q9NYK1	Toll-like receptor 7	TLR7	14	3
Q9NYK5	Large ribosomal subunit protein mL39	MRPL39 C21orf92 MRPL5 RPML5	0	1
Q9NYL4	Peptidyl-prolyl cis-trans isomerase FKBP11	FKBP11 FKBP19	3	2
Q9NYL9	Tropomodulin-3	TMOD3	1	1
Q9NYM4	G-protein coupled receptor 83	GPR83 GPR72 JP05 KIAA1540	3	0
Q9NYP7	Very long chain fatty acid elongase 5	ELOVL5 ELOVL2	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	5	0
Q9NYP9	Protein Mis18-alpha	MIS18A C21orf45 C21orf46 FASP1	2	1
Q9NYQ6	Cadherin EGF LAG seven-pass G-type receptor 1	CELSR1 CDHF9 FMI2	30	46
Q9NYQ7	Cadherin EGF LAG seven-pass G-type receptor 3	CELSR3 CDHF11 EGFL1 FMI1 KIAA0812 MEGF2	20	4
Q9NYQ8	Protocadherin Fat 2	FAT2 CDHF8 KIAA0811 MEGF1	40	2
Q9NYU1	UDP-glucose:glycoprotein glucosyltransferase 2	UGGT2 UGCGL2 UGT2	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	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

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