GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **112551 - 112575** 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
Q9UP38	Frizzled-1	FZD1	Homo sapiens (human)	4	3
Q9D2Z1	Carcinoembryonic antigen-related cell adhesion molecule 20	Ceacam20	Mus musculus (house mouse)	4	1
P58755	Lymphocyte antigen 96	LY96 MD2	Cricetulus griseus (Chinese hamster)	4	0
Q6P905	CD48 antigen	Cd48	Mus musculus (house mouse)	4	0
A0A0R4J0A4	receptor protein-tyrosine kinase	Flt1	Mus musculus (house mouse)	4	0
A2VCP3	P2X purinoceptor (Fragment)	P2rx7	Mus musculus (house mouse)	4	0
Q64K32	Subtilisin-like protease 5	SUB5	Trichophyton benhamiae	4	0
J9VQ06	Chitin synthase 2	CHS2	Cryptococcus neoformans var. grubii H99	4	0
Q9Z1P4	Leucine-rich repeat-containing G-protein coupled receptor 5	Lgr5 Fex Gpr49	Mus musculus (house mouse)	4	0
P14432	H-2 class I histocompatibility antigen, TLA(B) alpha chain	H2-T3	Mus musculus (house mouse)	4	0
P41221	Protein Wnt-5a	WNT5A	Homo sapiens (human)	4	10
Q27459	Acetylcholinesterase 1	ace-1	Caenorhabditis briggsae	4	0
Q3TD49	Signal peptide peptidase-like 2B	Sppl2b	Mus musculus (house mouse)	4	2
P19238	T-cell surface glycoprotein CD5	CD5	Bos taurus (cattle)	4	0
Q05910	Disintegrin and metalloproteinase domain-containing protein 8	Adam8 Ms2	Mus musculus (house mouse)	4	0
O61213	Dual oxidase 1	bli-3	Caenorhabditis elegans	4	0
Q1LW89	N-acetylneuraminate 9-O-acetyltransferase	casd1	Danio rerio (zebrafish)	4	0
A0MD34	Glycoprotein 5	GP5	PRRSV SD 01-08	4	0
A0A0C4DGH0	CD276 molecule	CD276	Homo sapiens (human)	4	0
Q7TQG5	Neogenin	Neo1	Mus musculus (house mouse)	4	0
P40939	Trifunctional enzyme subunit alpha, mitochondrial	HADHA HADH	Homo sapiens (human)	4	4	Barth syndrome HELLP syndrome Norum disease Reye syndrome Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia acquired immunodeficiency syndrome adult respiratory distress syndrome agnosia alpha 1-antitrypsin deficiency alternating exotropia amyotrophic lateral sclerosis arthritis arthropathy blindness breast cancer bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease cholestasis choreaacanthocytosis clubfoot cone-rod dystrophy congenital adrenal hyperplasia congenital stationary night blindness 1A congenital stationary night blindness congestive heart failure coronary artery disease cystinuria cytochrome-c oxidase deficiency disease developmental coordination disorder diabetes mellitus 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 disease of metabolism endomyocardial fibrosis epilepsy exotropia familial hypertrophic cardiomyopathy familial periodic paralysis fibromyalgia fundus albipunctatus galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemophagocytic lymphohistiocytosis hepatitis C human immunodeficiency virus infectious disease hypercalcemia hypertrophic cardiomyopathy hypoglycemia hypolipoproteinemia hypoparathyroidism inflammatory bowel disease inherited metabolic disorder intellectual disability lactic acidosis learning disability liver disease lung benign neoplasm lung cancer lung carcinoma metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse monocular exotropia myoglobinuria myopathy myopia myositis nephrocalcinosis neuropathy newborn respiratory distress syndrome night blindness obesity obsolete asthenopia osteoarthritis peripheral nervous system disease phosphorus metabolism disease placental insufficiency polyneuropathy pre-eclampsia progressive muscular atrophy prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinal disease retinitis pigmentosa retinitis sick sinus syndrome staphyloma posticum steatotic liver disease sudden infant death syndrome tricuspid valve insufficiency type 2 diabetes mellitus urea cycle disorder visual epilepsy von Willebrand's disease 2 von Willebrand's disease
Q63953	Ifngr2 protein	Ifngr2 ifngr2	Mus musculus (house mouse)	4	5
Q8R464	Cell adhesion molecule 4	Cadm4 Igsf4c Necl4 Tsll2	Mus musculus (house mouse)	4	16
P70392	Ras-specific guanine nucleotide-releasing factor 2	Rasgrf2 Grf2	Mus musculus (house mouse)	4	2
O08789	Max-binding protein MNT	Mnt Rox	Mus musculus (house mouse)	4	1

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