GlyCosmos Portal

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GlyConnect	April 19, 2023
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GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
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Displaying entries **13226 - 13250** 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
Q8VDK4	Cadherin 13	Cdh13	Mus musculus (house mouse)	5	0
Q16581	C3a anaphylatoxin chemotactic receptor	C3AR1 AZ3B C3R1 HNFAG09	Homo sapiens (human)	5	2
Q2H102	GPI inositol-deacylase	BST1	Chaetomium globosum CBS 148.51	5	0
P12572	Fusion glycoprotein F0	F	Newcastle disease virus (STRAIN AUSTRALIA-VICTORIA/32)	5	0
Q9CY42	Beta-2-glycoprotein 1	Apoh	Mus musculus (house mouse)	5	0
Q6V9Y8	Glypican-3	gpc3	Danio rerio (zebrafish)	5	0
B5A929	Soluble MET variant 1	MET	Homo sapiens (human)	5	0
Q96KG7	Multiple epidermal growth factor-like domains protein 10	MEGF10 KIAA1780	Homo sapiens (human)	5	0
Q9VAP3	Choline transporter-like 2	Ctl2	Drosophila melanogaster (fruit fly)	5	0
P04468	Kappa-casein	Csn3 Csn10 Csnk	Rattus norvegicus (Norway rat)	5	0
Q96HA4	Uncharacterized protein C1orf159	C1orf159	Homo sapiens (human)	5	3
Q8TGB2	GPI ethanolamine phosphate transferase 2	GPI7 LAS21	Candida albicans SC5314	5	0
Q6DEL2	Putative lipid scramblase CLPTM1	clptm1	Danio rerio (zebrafish)	5	0
Q07541	ER export of PMA1 protein 1	EXP1	Saccharomyces cerevisiae S288C	5	1
Q680B7	Endo-1,4-beta-xylanase 4	XYN4	Arabidopsis thaliana (thale cress)	5	0
Q9IKB5	Envelopment polyprotein	GP	Tomato spotted wilt virus (strain Regular2A)	5	0
P19697	Hemagglutinin	HA	Influenza A virus (A/duck/New Zealand/31/1976(H4N6))	5	0
Q64213	Splicing factor 1	Sf1 Zfm1 Zfp162	Mus musculus (house mouse)	5	1
Q8CFZ4	Glypican-3	Gpc3	Mus musculus (house mouse)	5	0
Q2UPC7	Flavin-dependent halogenase aclH	aclH	Aspergillus oryzae RIB40	5	0
P40533	Protein TED1	TED1	Saccharomyces cerevisiae S288C	5	0
Q68CP4	Heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT TMEM76	Homo sapiens (human)	5	19	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
Q6R2J8	Protein STRUBBELIG-RECEPTOR FAMILY 8	SRF8	Arabidopsis thaliana (thale cress)	5	0
Q9H156	SLIT and NTRK-like protein 2	SLITRK2 CXorf2 KIAA1854 SLITL1	Homo sapiens (human)	5	2
G5EFP5	Alpha-(1,3)-fucosyltransferase fut-3	fut-3 CEFT-4	Caenorhabditis elegans	5	0

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