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 **5151 - 5175** 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
Q9Y5W7	Sorting nexin-14	SNX14	Homo sapiens (human)	0	1
Q9Y5W5	Wnt inhibitory factor 1	WIF1	Homo sapiens (human)	2	0
Q9Y5W3	Krueppel-like factor 2	KLF2 LKLF	Homo sapiens (human)	0	1
Q9Y5V3	Melanoma-associated antigen D1	MAGED1 NRAGE	Homo sapiens (human)	2	1
Q9Y5V0	Zinc finger protein 706	ZNF706	Homo sapiens (human)	0	1
Q9Y5U5	Tumor necrosis factor receptor superfamily member 18	TNFRSF18 AITR GITR	Homo sapiens (human)	1	0
Q9Y5U2	U5 small nuclear ribonucleoprotein TSSC4	TSSC4	Homo sapiens (human)	1	1
Q9Y5T4	DnaJ homolog subfamily C member 15	DNAJC15 DNAJD1	Homo sapiens (human)	3	1
Q9Y5S9	RNA-binding protein 8A	RBM8A RBM8	Homo sapiens (human)	0	1
Q9Y5S8	NADPH oxidase 1	NOX1 MOX1 NOH1	Homo sapiens (human)	2	1
Q9Y5S2	Serine/threonine-protein kinase MRCK beta	CDC42BPB KIAA1124	Homo sapiens (human)	2	2
Q9Y5S1	Transient receptor potential cation channel subfamily V member 2	TRPV2 VRL	Homo sapiens (human)	1	0
Q9Y5R5	Doublesex- and mab-3-related transcription factor 2	DMRT2 DSXL2	Homo sapiens (human)	0	1
Q9Y5Q9	General transcription factor 3C polypeptide 3	GTF3C3	Homo sapiens (human)	0	1
Q9Y5Q5	Atrial natriuretic peptide-converting enzyme	CORIN CRN TMPRSS10	Homo sapiens (human)	19	1
Q9Y5P6	Mannose-1-phosphate guanyltransferase beta	GMPPB	Homo sapiens (human)	0	1	Bell's palsy Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Lambert-Eaton myasthenic syndrome Walker-Warburg syndrome agnosia amblyopia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness cardiomyopathy cataract centronuclear myopathy cleft palate clubfoot coloboma communicating hydrocephalus cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy A14 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy esotropia facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia idiopathic generalized epilepsy intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy mechanical strabismus megalocornea meningocele microcephaly microphthalmia monocular esotropia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy oligohydramnios ophthalmoplegia optic atrophy pathologic nystagmus ptosis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss speech disorder spontaneous ocular nystagmus strabismic amblyopia strabismus syndromic X-linked intellectual disability 94 visual epilepsy
Q9Y5P4	Ceramide transfer protein	CERT1 CERT COL4A3BP STARD11	Homo sapiens (human)	0	1
Q9Y5P1	Olfactory receptor 51B2	OR51B2 OR51B1P	Homo sapiens (human)	1	1
Q9Y5P0	Olfactory receptor 51B4	OR51B4	Homo sapiens (human)	1	0
Q9Y5N1	Histamine H3 receptor	HRH3 GPCR97	Homo sapiens (human)	1	0
Q9Y5M8	Signal recognition particle receptor subunit beta	SRPRB	Homo sapiens (human)	5	2
Q9Y5L3	Ectonucleoside triphosphate diphosphohydrolase 2	ENTPD2 CD39L1	Homo sapiens (human)	7	50
Q9Y5L2	Hypoxia-inducible lipid droplet-associated protein	HILPDA C7orf68 HIG2	Homo sapiens (human)	6	1
Q9Y5L0	Transportin-3	TNPO3 IPO12	Homo sapiens (human)	0	1
Q9Y5K6	CD2-associated protein	CD2AP	Homo sapiens (human)	5	1

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