GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9H2Y7	Zinc finger protein 106	ZNF106 SH3BP3 ZFP106 ZNF474	8	4
Q9H2Y9	Solute carrier organic anion transporter family member 5A1	SLCO5A1 OATP5A1 SLC21A15	7	0
Q9H2Z4	Homeobox protein Nkx-2.4	NKX2-4 NKX2D	0	1
Q9H306	Matrix metalloproteinase-27	MMP27	3	1
Q9H307	Pinin	PNN DRS MEMA	1	1
Q9H310	Ammonium transporter Rh type B	RHBG	1	0
Q9H313	Protein tweety homolog 1	TTYH1	4	0
Q9H324	A disintegrin and metalloproteinase with thrombospondin motifs 10	ADAMTS10	7	3
Q9H329	Band 4.1-like protein 4B	EPB41L4B EHM2 LULU2	3	1
Q9H330	Transmembrane protein 245	TMEM245 C9orf5	6	16
Q9H334	Forkhead box protein P1	FOXP1	10	2
Q9H340	Olfactory receptor 51B6	OR51B6	1	0
Q9H341	Olfactory receptor 51M1	OR51M1	1	0
Q9H342	Olfactory receptor 51J1	OR51J1 OR51J1P OR51J2	1	0
Q9H344	Olfactory receptor 51I2	OR51I2	1	0
Q9H346	Olfactory receptor 52D1	OR52D1	1	0
Q9H347	Ubiquilin-3	UBQLN3	1	1
Q9H361	Polyadenylate-binding protein 3	PABPC3 PABP3 PABPL3	3	2
Q9H379	Putative uncharacterized protein PRO3102	PRO3102	0	1
Q9H3C8	Truncated epidermal growth factor receptor (Fragment)	EGFR	1	0
Q9H3D0	A431-specific truncated epidermal growth factor receptor (Fragment)	EGFR	1	0
Q9H3E2	Sorting nexin-25	SNX25	0	1
Q9H3G5	Probable serine carboxypeptidase CPVL	CPVL VLP	5	109
Q9H3H1	tRNA dimethylallyltransferase	TRIT1 IPT MOD5	1	2
Q9H3H5	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	DPAGT1 DPAGT2	2	2	Bell's palsy Ebola hemorrhagic fever Lambert-Eaton myasthenic syndrome acute intermittent porphyria agnosia alternating exotropia breast cancer cancer cataract clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ij congenital disorder of glycosylation type I congenital disorder of glycosylation congenital myasthenic syndrome 13 congenital myasthenic syndrome congenital nystagmus congenital ptosis cutaneous leishmaniasis developmental and epileptic encephalopathy 36 developmental coordination disorder dissociated nystagmus epilepsy essential hypertension exotropia facial nerve disease facial paralysis familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome glycoproteinosis hepatocellular carcinoma hypertension intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability leishmaniasis liver cancer microcephaly monocular exotropia mucolipidosis II alpha/beta myopathy pathologic nystagmus pseudosarcomatous fibromatosis ptosis scoliosis spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma stuttering syndromic X-linked intellectual disability 94 tongue squamous cell carcinoma tuberculosis visceral leishmaniasis visual epilepsy

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