GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q13765	Nascent polypeptide-associated complex subunit alpha	NACA	0	1
Q96RT6	cTAGE family member 2	CTAGE1 CTAGE2	0	1
P61009	Signal peptidase complex subunit 3	SPCS3 SPC22	1	1
Q9BVI0	PHD finger protein 20	PHF20 C20orf104 GLEA2 HCA58 NZF TZP	0	1
O60942	mRNA-capping enzyme	RNGTT CAP1A	0	1
Q99871	HAUS augmin-like complex subunit 7	HAUS7 UCHL5IP UIP1	0	1
P36957	Dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial	DLST DLTS	2	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 Joubert syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Wernicke-Korsakoff syndrome adrenal gland cancer amnestic disorder aniridia cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cortical dysplasia-focal epilepsy syndrome duodenum cancer glomerulonephritis heart cancer hydranencephaly hypercalcemia hypertensive retinopathy kidney disease lissencephaly nephritis nephrocalcinosis neurodegenerative disease panic disorder papillary renal cell carcinoma paraganglioma pheochromocytoma phosphorus metabolism disease pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary biliary cholangitis prostate cancer prostate carcinoma proteinuria renal carcinoma renal cell carcinoma renal osteodystrophy sarcomatoid renal cell carcinoma septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly small intestine cancer syndromic X-linked intellectual disability Najm type
P33240	Cleavage stimulation factor subunit 2	CSTF2	3	1
P15153	Ras-related C3 botulinum toxin substrate 2	RAC2	4	1
Q9NUG6	p53 and DNA damage-regulated protein 1	PDRG1 C20orf126 PDRG	0	1
A4FU49	SH3 domain-containing protein 21	SH3D21 C1orf113	1	1
Q9H0G5	Nuclear speckle splicing regulatory protein 1	NSRP1 CCDC55 NSRP70	0	1
P40261	Nicotinamide N-methyltransferase	NNMT	0	1
O60232	Protein ZNRD2	ZNRD2 SSSCA1	1	1
Q9BTK6	PAXIP1-associated glutamate-rich protein 1	PAGR1 C16orf53 PA1	4	1
Q86U37	Uncharacterized protein encoded by LINC01551	LINC01551 C14orf23	2	1
Q92974	Rho guanine nucleotide exchange factor 2	ARHGEF2 KIAA0651 LFP40	1	1
Q8TE82	SH3 domain and tetratricopeptide repeat-containing protein 1	SH3TC1	0	1
Q9BSK2	Solute carrier family 25 member 33	SLC25A33	0	1
P43088	Prostaglandin F2-alpha receptor	PTGFR	2	1
Q96BN8	Ubiquitin thioesterase otulin	OTULIN FAM105B	0	1
Q8NB16	Mixed lineage kinase domain-like protein	MLKL	4	1
Q96GM5	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1	SMARCD1 BAF60A	1	1
Q99569	Plakophilin-4	PKP4	2	1
O15480	Melanoma-associated antigen B3	MAGEB3	0	1

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