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 **107176 - 107200** 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
P41439	Folate receptor gamma	FOLR3	Homo sapiens (human)	3	0
Q5RAF4	Sialidase-1	NEU1	Pongo abelii (Sumatran orangutan)	3	0
O95754	Semaphorin-4F	SEMA4F SEMAM SEMAW	Homo sapiens (human)	3	2
Q3TN91	ABC transporter domain-containing protein (Fragment)	Abca3	Mus musculus (house mouse)	3	0
Q9USW2	Inheritance of peroxisomes protein 2	inp2	Schizosaccharomyces pombe 972h-	3	0
Q8MK48	Solute carrier family 22 member 6	SLC22A6 OAT1	Sus scrofa (pig)	3	0
Q9ET43	Claudin-12	Cldn12	Mus musculus (house mouse)	3	2
P48617	Erythropoietin	EPO	Bos taurus (cattle)	3	0
D5J9U8	Germacrene A hydroxylase	GAO1	Lactuca sativa (garden lettuce)	3	0
Q4R8Y9	Trophoblast glycoprotein	TPBG	Macaca fascicularis (crab-eating macaque)	3	0
B2ZI34	Neuromedin-B receptor	NMBR	Sus scrofa (pig)	3	0
Q3MI99	Collagen and calcium-binding EGF domain-containing protein 1	Ccbe1 Kiaa1983	Mus musculus (house mouse)	3	0
Q9JJL3	Solute carrier organic anion transporter family member 1B2	Slco1b2 Oatp1b2 Slc21a10	Mus musculus (house mouse)	3	0
Q791Q5	Als splice variant 1	Igfals Als	Mus musculus (house mouse)	3	0
Q8BH32	Sushi domain-containing protein 4	Susd4	Mus musculus (house mouse)	3	2
P49748	Very long-chain specific acyl-CoA dehydrogenase, mitochondrial	ACADVL VLCAD	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 Clouston syndrome Pearson syndrome Pick's disease Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 adrenal adenoma adrenal cortex cancer alpha 1-antitrypsin deficiency atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrioventricular block cardiomyopathy catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cerebral degeneration complement component 2 deficiency congenital adrenal hyperplasia dermatitis dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy endomyocardial fibrosis familial hypertrophic cardiomyopathy familial periodic paralysis gallbladder disease hemopericardium hypercalcemia hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels lactic acidosis liver disease macroglobulinemia metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency myopathy nephrocalcinosis obesity obsolete lymphoplasmacytic lymphoma patent foramen ovale pericardial effusion phosphorus metabolism disease placental insufficiency pneumonia pseudosarcomatous fibromatosis sensorineural hearing loss steatotic liver disease urea cycle disorder ventricular septal defect very long chain acyl-CoA dehydrogenase deficiency von Willebrand's disease 2 von Willebrand's disease
B1AWL2	Zinc finger protein 462	Znf462 Zfp462	Mus musculus (house mouse)	3	1
Q864L3	Sodium channel subunit beta-2	SCN2B	Canis lupus familiaris (dog)	3	0
A7E2V4	Zinc finger SWIM domain-containing protein 8	ZSWIM8 KIAA0913	Homo sapiens (human)	3	2
P28026	Protein Wnt-8	wnt8	Xenopus laevis (African clawed frog)	3	0
Q6T3A5	PKHD1	Pkhd1	Mus musculus (house mouse)	3	0
E4UVK2	Extracellular metalloproteinase 5	MEP5	Nannizzia gypsea CBS 118893	3	0
O14764	Gamma-aminobutyric acid receptor subunit delta	GABRD	Homo sapiens (human)	3	3
Q8SPU5	BPI fold-containing family A member 1	BPIFA1 PLUNC	Bos taurus (cattle)	3	0
Q02253	Methylmalonate-semialdehyde/malonate-semialdehyde dehydrogenase [acylating], mitochondrial	Aldh6a1 Mmsdh	Rattus norvegicus (Norway rat)	3	1

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