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 **426 - 450** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A0A2K4X4G7	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
I2GUK6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9H0B3	IQ domain-containing protein N	IQCN KIAA1683	Homo sapiens (human)	0	1
Q96RN5	Mediator of RNA polymerase II transcription subunit 15	MED15 ARC105 CTG7A PCQAP TIG1 TNRC7	Homo sapiens (human)	12	1
E7BYD4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A1S5QR61	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8N145	Leucine-rich repeat LGI family member 3	LGI3 LGIL4	Homo sapiens (human)	2	0
Q8IWA5	Choline transporter-like protein 2	SLC44A2 CTL2	Homo sapiens (human)	4	24
Q8NH69	Olfactory receptor 5W2	OR5W2 OR5W2P OR5W3P	Homo sapiens (human)	1	0
Q9NNW5	tRNA (34-2'-O)-methyltransferase regulator WDR6	WDR6	Homo sapiens (human)	1	1
P00738	Haptoglobin	HP	Homo sapiens (human)	7	299
F1JVV5	EWSR1/ATF1 fusion protein type 1	EWSR1/ATF1 fusion	Homo sapiens (human)	0	1
Q8NC54	Keratinocyte-associated transmembrane protein 2	KCT2 C5orf15	Homo sapiens (human)	5	2
F8SKV9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
F2X5U9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P35499	Sodium channel protein type 4 subunit alpha	SCN4A	Homo sapiens (human)	13	8
Q92610	Zinc finger protein 592	ZNF592 KIAA0211	Homo sapiens (human)	6	2
P17050	Alpha-N-acetylgalactosaminidase	NAGA	Homo sapiens (human)	5	95	Clouston syndrome Fabry disease Kanzaki disease Schindler disease type 1 Unverricht-Lundborg syndrome acquired hyperkeratosis alternating hemiplegia of childhood autistic disorder autonomic neuropathy blepharospasm cancer cardiomyopathy cataract central nervous system disease central nervous system origin vertigo cerebral degeneration chylomicron retention disease congenital nystagmus dissociated nystagmus early myoclonic encephalopathy elephantiasis embryoma endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy focal hand dystonia gallbladder disease hypertrophic cardiomyopathy hypertropia influenza intellectual disability learning disability lipid storage disease liver disease lymphedema mechanical strabismus nervous system disease neuroaxonal dystrophy neurodegeneration with brain iron accumulation 2a neuropathy ophthalmoplegia optic atrophy pathologic nystagmus peripheral nervous system disease sensorineural hearing loss spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 trichomoniasis visual epilepsy
A0A1C3PHQ8	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q9HD43	Receptor-type tyrosine-protein phosphatase H	PTPRH SAP1	Homo sapiens (human)	10	0
O14745	Na(+)/H(+) exchange regulatory cofactor NHE-RF1	NHERF1 NHERF SLC9A3R1	Homo sapiens (human)	0	1
Q9ULL0	Acrosomal protein KIAA1210	KIAA1210	Homo sapiens (human)	4	1
B5A939	Soluble MET variant 11	MET	Homo sapiens (human)	3	0
P07093	Glia-derived nexin	SERPINE2 PI7 PN1	Homo sapiens (human)	5	12
Q68CP9	AT-rich interactive domain-containing protein 2	ARID2 BAF200 KIAA1557	Homo sapiens (human)	19	2

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