GlyCosmos Portal

Displaying entries **3526 - 3550** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q92541	RNA polymerase-associated protein RTF1 homolog	RTF1 KIAA0252	3	1
Q149N8	E3 ubiquitin-protein ligase SHPRH	SHPRH KIAA2023	0	1
Q6P9A3	Zinc finger protein 549	ZNF549	2	1
Q9Y6A2	Cholesterol 24-hydroxylase	CYP46A1 CYP46	2	1	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 Creutzfeldt-Jakob disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lennox-Gastaut syndrome Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 age related macular degeneration amyloidosis brain disease cancer cardiac arrest cerebral degeneration cerebrovascular disease chronic fatigue syndrome colorectal cancer colorectal carcinoma degeneration of macula and posterior pole depressive disorder diabetes mellitus dysthymic disorder encephalitis encephalomyelitis giant cell glioblastoma glioblastoma high grade glioma large intestine cancer macular degeneration major depressive disorder melancholic depression multiple sclerosis myelitis neurodegenerative disease neurotic disorder obsolete melancholia primary open angle glaucoma tauopathy type 2 diabetes mellitus
Q6BDS2	Bridge-like lipid transfer protein family member 3A	BLTP3A C6orf107 UHRF1BP1	1	1
Q8N8E3	Centrosomal protein of 112 kDa	CEP112 CCDC46	0	1
Q9UKS6	Protein kinase C and casein kinase substrate in neurons protein 3	PACSIN3	0	1
O43837	Isocitrate dehydrogenase [NAD] subunit beta, mitochondrial	IDH3B	0	1	Zollinger-Ellison syndrome bipolar disorder blindness cataract cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus eye disease fundus albipunctatus fundus dystrophy glaucoma hidradenitis suppurativa hidradenitis hyperinsulinism hypogonadism intellectual disability keratoconus learning disability obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus pompholyx retinitis pigmentosa 46 retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma type 2 diabetes mellitus
Q14934	Nuclear factor of activated T-cells, cytoplasmic 4	NFATC4 NFAT3	0	1
Q99471	Prefoldin subunit 5	PFDN5 MM1 PFD5	0	1
P11177	Pyruvate dehydrogenase E1 component subunit beta, mitochondrial	PDHB PHE1B	2	1	Leigh disease acute myocardial infarction breast cancer breast carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary thrombosis diabetes mellitus lactic acidosis luminal breast carcinoma A melanoma myocardial infarction nonpapillary renal cell carcinoma papillary adenocarcinoma papillary renal cell carcinoma pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma thyroid gland papillary carcinoma type 2 diabetes mellitus
Q96RT1	Erbin	ERBIN ERBB2IP KIAA1225 LAP2	2	1
Q00536	Cyclin-dependent kinase 16	CDK16 PCTAIRE1 PCTK1	0	1
Q2M2H8	Probable maltase-glucoamylase 2	MGAM2	5	1
Q96RD6	Pannexin-2	PANX2	2	1
Q9HCD6	Protein TANC2	TANC2 KIAA1148 KIAA1636	12	1
Q9Y6K5	2'-5'-oligoadenylate synthase 3	OAS3	1	1
Q8WW59	SPRY domain-containing protein 4	SPRYD4	1	1
Q99814	Endothelial PAS domain-containing protein 1	EPAS1 BHLHE73 HIF2A MOP2 PASD2	0	1
P11277	Spectrin beta chain, erythrocytic	SPTB SPTB1	6	1
A0A0U1RQS6	Transmembrane protein 275	TMEM275	1	1
Q3MHD2	Protein LSM12	LSM12	0	1
A6NL88	Protein shisa-7	SHISA7	4	1
P0DMB2	Uncharacterized protein C8orf88	C8orf88	0	1
Q9ULV3	Cip1-interacting zinc finger protein	CIZ1 LSFR1 NP94 ZNF356	0	1

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