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 **11101 - 11125** 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
Q2QYW3	Xylan O-acetyltransferase 3	XOAT3 TBL9	Oryza sativa Japonica Group (Japanese rice)	5	0
Q8K4G1	Latent-transforming growth factor beta-binding protein 4	Ltbp4	Mus musculus (house mouse)	5	0
A0A8J9WHR9	ABC-type transporter phomO	phomO	Diaporthe leptostromiformis	5	0
Q2M2H8	Probable maltase-glucoamylase 2	MGAM2	Homo sapiens (human)	5	1
Q5J316	Solute carrier family 2, facilitated glucose transporter member 12	SLC2A12 GLUT12	Bos taurus (cattle)	5	0
O61460	Ephrin receptor 1	vab-1	Caenorhabditis elegans	5	0
E2RP87	Low affinity immunoglobulin gamma Fc region receptor III-A	FCGR3A	Canis lupus familiaris (dog)	5	0
Q3U254	EMILIN-1	Emilin1	Mus musculus (house mouse)	5	0
Q8NC54	Keratinocyte-associated transmembrane protein 2	KCT2 C5orf15	Homo sapiens (human)	5	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
P07093	Glia-derived nexin	SERPINE2 PI7 PN1	Homo sapiens (human)	5	12
Q9XI78	Probable fucosyltransferase 8	FUT8	Arabidopsis thaliana (thale cress)	5	0
P14842	5-hydroxytryptamine receptor 2A	Htr2a Htr2	Rattus norvegicus (Norway rat)	5	0
Q8L608	Heparanase-like protein 2	At5g61250	Arabidopsis thaliana (thale cress)	5	0
Q07912	Activated CDC42 kinase 1	TNK2 ACK1	Homo sapiens (human)	5	1
Q8BUV3	Gephyrin	Gphn	Mus musculus (house mouse)	5	1
O35632	Hyaluronidase-2	Hyal2	Mus musculus (house mouse)	5	4
Q9UW98	Dipeptidyl-peptidase 5	DPPV	Trichophyton rubrum	5	0
O81291	L-type lectin-domain containing receptor kinase IV.4	LECRK44	Arabidopsis thaliana (thale cress)	5	0
P24593	Insulin-like growth factor-binding protein 5	IGFBP5 IBP5	Homo sapiens (human)	5	2
P02763	Alpha-1-acid glycoprotein 1	ORM1 AGP1	Homo sapiens (human)	5	237
Q90812	Corticotropin-releasing factor receptor 1	CRHR1	Gallus gallus (chicken)	5	0
P63244	Small ribosomal subunit protein RACK1	RACK1 GNB2L1	Homo sapiens (human)	5	1
Q54F25	Battenin	cln3	Dictyostelium discoideum	5	0
Q9NU22	Midasin	MDN1 KIAA0301	Homo sapiens (human)	5	11

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