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 **13026 - 13050** 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
P10923	Osteopontin	Spp1 Eta-1 Op Spp-1	Mus musculus (house mouse)	5	0
Q5R9M9	Zinc transporter ZIP6	SLC39A6 ZIP6	Pongo abelii (Sumatran orangutan)	5	0
Q60513	Low affinity immunoglobulin gamma Fc region receptor II	FCGR2	Cavia porcellus (domestic guinea pig)	5	0
P92982	Polygalacturonase 1 beta-like protein 1	PGL1 JP630 PG3	Arabidopsis thaliana (thale cress)	5	0
Q9GYF0	Cholesterol uptake protein 1	chup-1 cup-1 tag-130	Caenorhabditis elegans	5	0
O04500	COBRA-like protein 6	COBL6	Arabidopsis thaliana (thale cress)	5	0
Q9QZF2	Glypican-1	Gpc1	Mus musculus (house mouse)	5	3
Q9LMX4	Probable inactive purple acid phosphatase 1	PAP1	Arabidopsis thaliana (thale cress)	5	0
Q9H5K3	Protein O-mannose kinase	POMK SGK196	Homo sapiens (human)	5	9	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia 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 coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
Q9S9M2	Wall-associated receptor kinase-like 4	WAKL4	Arabidopsis thaliana (thale cress)	5	0
P21077	Soluble interferon alpha/beta receptor OPG204	OPG204	Vaccinia virus Copenhagen	5	0
C1HC91	Leucine aminopeptidase 1	LAP1	Paracoccidioides lutzii Pb01	5	0
Q1ENI8	Peroxidasin homolog pxn-1	pxn-1	Caenorhabditis elegans	5	0
O75147	Obscurin-like protein 1	OBSL1 KIAA0657	Homo sapiens (human)	5	1
Q3TYU2	Probable cation-transporting ATPase 13A5	Atp13a5	Mus musculus (house mouse)	5	3
P33146	Cadherin-15	Cdh15 Cdh14	Mus musculus (house mouse)	5	5
P08934	Kininogen-1	Kng1 Kng	Rattus norvegicus (Norway rat)	5	0
Q3TAN0	Cadherin domain-containing protein	Cdh17	Mus musculus (house mouse)	5	0
C8ZAZ9	VPS10 homolog 2	VTH2	Saccharomyces cerevisiae EC1118	5	0
Q9NUL3	Double-stranded RNA-binding protein Staufen homolog 2	STAU2	Homo sapiens (human)	5	2
Q3TDQ1	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3B	Stt3b Simp	Mus musculus (house mouse)	5	8
Q969V6	Myocardin-related transcription factor A	MRTFA KIAA1438 MAL MKL1	Homo sapiens (human)	5	2
Q9Z0Y8	Voltage-dependent T-type calcium channel subunit alpha-1I	Cacna1i	Rattus norvegicus (Norway rat)	5	0
Q9LDM5	Putative cysteine-rich receptor-like protein kinase 31	CRK31	Arabidopsis thaliana (thale cress)	5	0
Q8BLI4	Dermatan-sulfate epimerase	Dse Sart2	Mus musculus (house mouse)	5	0

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