GlyCosmos Portal

Source	Last Updated
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 **107526 - 107550** 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
P09812	Glycogen phosphorylase, muscle form	Pygm	Rattus norvegicus (Norway rat)	0	1
Q9H4L4	Sentrin-specific protease 3	SENP3 SSP3 SUSP3	Homo sapiens (human)	0	1
A6NGU7	Putative uncharacterized protein encoded by LINC01546	LINC01546 CXorf28	Homo sapiens (human)	1	1
Q6ZWJ1	Syntaxin-binding protein 4	STXBP4	Homo sapiens (human)	0	1
Q3UND0	Src kinase-associated phosphoprotein 2	Skap2 Prap Ra70 Saps Scap2 Skap55r	Mus musculus (house mouse)	0	1
Q92844	TRAF family member-associated NF-kappa-B activator	TANK ITRAF TRAF2	Homo sapiens (human)	2	1
Q12882	Dihydropyrimidine dehydrogenase [NADP(+)]	DPYD	Homo sapiens (human)	4	1
P30559	Oxytocin receptor	OXTR	Homo sapiens (human)	3	1
Q8CDI6	Coiled-coil domain-containing protein 158	Ccdc158	Mus musculus (house mouse)	2	1
Q15024	Exosome complex component RRP42	EXOSC7 KIAA0116 RRP42	Homo sapiens (human)	0	1
F7BQE4	Rho guanine nucleotide exchange factor (GEF) 10 (Fragment)	Arhgef10	Mus musculus (house mouse)	0	1
Q4DPM2	N-terminal region of Chorein, a TM vesicle-mediated sorter family protein (Fragment)	Tc00.1047053507083.109	Trypanosoma cruzi strain CL Brener	0	1
P62630	Elongation factor 1-alpha 1	Eef1a1 Eef1a	Rattus norvegicus (Norway rat)	0	1
Q8CCS6	Polyadenylate-binding protein 2	Pabpn1 Pab2 Pabp2	Mus musculus (house mouse)	0	1
P50416	Carnitine O-palmitoyltransferase 1, liver isoform	CPT1A CPT1	Homo sapiens (human)	3	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 D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy
P0DKV0	Putative spermatogenesis-associated protein 31C1	SPATA31C1 FAM75C1	Homo sapiens (human)	0	1
O43790	Keratin, type II cuticular Hb6	KRT86 KRTHB6	Homo sapiens (human)	0	1
P56177	Homeobox protein DLX-1	DLX1	Homo sapiens (human)	0	1
Q9SZ51	Early nodulin-like protein 15	ENODL15 EN15	Arabidopsis thaliana (thale cress)	1	1
Q96J77	Tumor protein D55	TPD52L3	Homo sapiens (human)	0	1
Q9H4S2	GS homeobox 1	GSX1 GSH1	Homo sapiens (human)	1	1
Q9VXY5	LP17418p	Cox17 CG9065-RA COXS Dmel\CG9065	Drosophila melanogaster (fruit fly)	0	1
P06730	Eukaryotic translation initiation factor 4E	EIF4E EIF4EL1 EIF4F	Homo sapiens (human)	2	1
B6SEH8	Endogenous retrovirus group V member 1 Env polyprotein	ERVV-1 ENVV1	Homo sapiens (human)	2	1
Q8VCW8	Medium-chain acyl-CoA ligase ACSF2, mitochondrial	Acsf2	Mus musculus (house mouse)	0	1

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