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 **14976 - 15000** 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
Q5R5F6	Haptoglobin	HP	Pongo abelii (Sumatran orangutan)	4	0
B6DZD0	Fructan 1-exohydrolase	1-FEH	Triticum urartu	4	0
B0XQB2	Probable alpha-L-arabinofuranosidase C	abfC	Aspergillus fumigatus A1163	4	0
Q80WT4	G-protein coupled receptor 176	Gpr176 Agr9 Gm1012	Mus musculus (house mouse)	4	0
Q99MB3	TM2 domain-containing protein 1	Tm2d1 Bbp	Mus musculus (house mouse)	4	0
Q07553	Guanylate cyclase 32E	Gyc32E GC	Drosophila melanogaster (fruit fly)	4	0
E5RKG2	Scavenger receptor FEEL-2c	Stab2 MFEEL-2	Mus musculus (house mouse)	4	0
Q63120	ATP-binding cassette sub-family C member 2	Abcc2 Cmoat Cmrp Mrp2	Rattus norvegicus (Norway rat)	4	0
O75534	Cold shock domain-containing protein E1	CSDE1 D1S155E KIAA0885 NRU UNR	Homo sapiens (human)	4	2
O00584	Ribonuclease T2	RNASET2 RNASE6PL	Homo sapiens (human)	4	24
E1ACP9	FAD-linked oxidoreductase notD	notD	Aspergillus sp. MF297-2	4	0
P25236	Selenoprotein P	Selenop Selp Sepp1	Rattus norvegicus (Norway rat)	4	0
Q9M2U5	Endochitinase EP3	EP3 CHIV	Arabidopsis thaliana (thale cress)	4	0
Q99K07	Enpp3 protein (Fragment)	Enpp3	Mus musculus (house mouse)	4	0
P02470	Alpha-crystallin A chain	CRYAA CRYA1	Bos taurus (cattle)	4	1
Q5RDQ8	Metabotropic glutamate receptor 7	GRM7	Pongo abelii (Sumatran orangutan)	4	0
P51689	Arylsulfatase D	ARSD	Homo sapiens (human)	4	10	Asperger syndrome Bannayan-Riley-Ruvalcaba syndrome Beckwith-Wiedemann syndrome CLOVES syndrome Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Cowden syndrome Down syndrome Dubowitz syndrome Lown-Ganong-Levine syndrome Marfan syndrome Mowat-Wilson syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Perlman syndrome Prader-Willi syndrome Rett syndrome Richter's syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Sotos syndrome Williams-Beuren syndrome Wolff-Parkinson-White syndrome X-linked Aarskog syndrome acute kidney tubular necrosis acute myeloid leukemia acute promyelocytic leukemia adult respiratory distress syndrome alexia amnestic disorder aniridia anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve stenosis argininosuccinic aciduria arteriosclerotic cardiovascular disease atherosclerosis 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 atrioventricular septal defect attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bicuspid aortic valve disease breast cancer breast carcinoma buphthalmos cardiomyopathy cardiovascular system disease cerebral palsy chondrodysplasia-pseudohermaphroditism syndrome chronic lymphocytic leukemia citrullinemia communication disorder conduct disorder congenital heart disease congestive heart failure coronary artery disease depressive disorder developmental coordination disorder disease of mental health dyslexia dysthymic disorder eating disorder endocarditis endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy essential hypertension excessive tearing familial hypertrophic cardiomyopathy fragile X syndrome generalized anxiety disorder glaucoma heart disease hemiplegia hydrophthalmos hyperargininemia hypertension hypertrophic cardiomyopathy hypospadias immune system disease infective endocarditis intellectual disability juvenile glaucoma lacrimal apparatus disease language disorder learning disability major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia neurotic disorder newborn respiratory distress syndrome nicotine dependence obesity obsolete melancholia patent ductus arteriosus patent foramen ovale phobic disorder polycystic ovary syndrome post-traumatic stress disorder primary open angle glaucoma psychotic disorder pulmonary valve stenosis retrograde amnesia schizophrenia sclerocornea situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy subacute bacterial endocarditis substance abuse substance-related disorder supravalvular aortic stenosis syndromic X-linked intellectual disability 94 tuberous sclerosis ventricular septal defect visual epilepsy
Q9FNP2	GDSL esterase/lipase At5g08460	At5g08460	Arabidopsis thaliana (thale cress)	4	0
Q9SB38	Pectinesterase inhibitor 4	PMEI4	Arabidopsis thaliana (thale cress)	4	0
Q9H5Y7	SLIT and NTRK-like protein 6	SLITRK6	Homo sapiens (human)	4	1
Q9VLV7	Protein spaetzle 3	spz3	Drosophila melanogaster (fruit fly)	4	0
Q3ZPT5	Phenoloxidase 1	PPO1	Spodoptera litura	4	0
Q20963	Serpentine receptor class beta-13	srb-13	Caenorhabditis elegans	4	0
Q6YNB6	Follicle-stimulating hormone receptor	FSHR	Notamacropus eugenii (tammar wallaby)	4	0
Q6DIV5	Inactive serine protease PAMR1	pamr1 ramp	Xenopus tropicalis (tropical clawed frog)	4	0

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