GlyCosmos Portal

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Displaying entries **118001 - 118025** 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
A0A9L0KLL5	Angiotensin-converting enzyme	ACE	Equus asinus (ass)	7	0
Q5ATH9	Exo-1,4-beta-xylosidase bxlB	bxlB	Aspergillus nidulans FGSC A4	7	0
P04180	Phosphatidylcholine-sterol acyltransferase	LCAT	Homo sapiens (human)	7	28	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 Bloom syndrome Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Norum disease Pick's disease Reye syndrome Tangier disease abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acute chest syndrome acute myocardial infarction agenesis of the corpus callosum with peripheral neuropathy anemia aortic atherosclerosis arcus senilis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness brain stem infarction cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency choreaacanthocytosis chronic kidney disease chylomicron retention disease congestive heart failure corneal dystrophy coronary artery disease coronary thrombosis disease of metabolism dry eye syndrome familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial lipoprotein lipase deficiency familial nephrotic syndrome gallbladder disease glomerulonephritis granular corneal dystrophy heart disease hemolytic anemia hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hyperalphalipoproteinemia 1 hyperlipoproteinemia type V hypolipoproteinemia inherited metabolic disorder kidney disease kidney failure lipoid nephrosis liver cancer liver disease macrocytic anemia macular corneal dystrophy motor peripheral neuropathy myocardial infarction nephritis nephrosis nephrotic syndrome nutmeg liver obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum ovarian cancer ovarian carcinoma proteinuria pyoureter recurrent corneal erosion renal osteodystrophy rheumatoid arthritis sickle cell anemia silent myocardial infarction steatotic liver disease uremia xerophthalmia
Q9UJU6	Drebrin-like protein	DBNL CMAP SH3P7	Homo sapiens (human)	7	1
G4MWA7	FAD-linked oxidoreductase OXR2	OXR2	Pyricularia oryzae 70-15	7	0
P10092	Calcitonin gene-related peptide 2	CALCB CALC2	Homo sapiens (human)	7	1
P36166	Paxillin-like protein 1	PXL1	Saccharomyces cerevisiae S288C	7	1
P27169	Serum paraoxonase/arylesterase 1	PON1 PON	Homo sapiens (human)	7	55
P55204	Guanylyl cyclase C	GUCY2C GUC2C	Sus scrofa (pig)	7	0
P04792	Heat shock protein beta-1	HSPB1 HSP27 HSP28	Homo sapiens (human)	7	1
A8N5E6	Plasma membrane fusion protein PRM1	PRM1	Coprinopsis cinerea okayama7#130	7	0
Q91ZV7	Plexin domain-containing protein 1	Plxdc1 Tem7	Mus musculus (house mouse)	7	0
Q54TA1	Probable serine/threonine-protein kinase drkC	drkC rk3	Dictyostelium discoideum	7	0
Q9Y4B4	Helicase ARIP4	RAD54L2 ARIP4 KIAA0809	Homo sapiens (human)	7	2
B1H1P9	Lysosomal acid phosphatase	acp2	Xenopus laevis (African clawed frog)	7	0
A0A0A6YY09	Protocadherin 9	Pcdh9	Mus musculus (house mouse)	7	5
Q9V496	Apolipophorins	apolpp RfaBp Rfabg	Drosophila melanogaster (fruit fly)	7	0
Q653V7	Probable alpha-glucosidase Os06g0675700	Os06g0675700	Oryza sativa Japonica Group (Japanese rice)	7	0
Q06108	Regulator of the glycerol channel 1	RGC1	Saccharomyces cerevisiae S288C	7	1
P87498	Vitellogenin-1	VTG1 VTGI	Gallus gallus (chicken)	7	0
Q95237	L-selectin	SELL	Pan troglodytes (chimpanzee)	7	0
Q54FD8	Protein psiD	psiD	Dictyostelium discoideum	7	0
Q80WC7	Arf-GAP domain and FG repeat-containing protein 2	Agfg2 Hrbl Rabr	Mus musculus (house mouse)	7	1
Q2HXL6	ER degradation-enhancing alpha-mannosidase-like protein 3	Edem3	Mus musculus (house mouse)	7	3
Q8TE56	A disintegrin and metalloproteinase with thrombospondin motifs 17	ADAMTS17	Homo sapiens (human)	7	2

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