GlyCosmos Portal

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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 **2826 - 2850** 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
P59510	A disintegrin and metalloproteinase with thrombospondin motifs 20	ADAMTS20	Homo sapiens (human)	16	3
Q9EPU0	Regulator of nonsense transcripts 1	Upf1 Rent1	Mus musculus (house mouse)	4	3
Q8IUH4	Palmitoyltransferase ZDHHC13	ZDHHC13 HIP14L HIP3RP	Homo sapiens (human)	2	3
Q8BS35	Alkylglycerol monooxygenase	Agmo Tmem195	Mus musculus (house mouse)	1	3
P17182	Alpha-enolase	Eno1 Eno-1	Mus musculus (house mouse)	2	3
Q9QYK5	Heparan-sulfate 6-O-sulfotransferase 1	Hs6st1	Mus musculus (house mouse)	2	3
Q80UG5	Septin-9	Septin9 Kiaa0991 Sept9 Sint1	Mus musculus (house mouse)	4	3
Q8IW00	V-set and transmembrane domain-containing protein 4	VSTM4 C10orf72	Homo sapiens (human)	5	3
P23515	Oligodendrocyte-myelin glycoprotein	OMG OMGP	Homo sapiens (human)	12	3
O43432	Eukaryotic translation initiation factor 4 gamma 3	EIF4G3	Homo sapiens (human)	17	3
O89051	Integral membrane protein 2B	Itm2b	Mus musculus (house mouse)	1	3
O09118	Netrin-1	Ntn1	Mus musculus (house mouse)	4	3
Q658P3	Metalloreductase STEAP3	STEAP3 TSAP6	Homo sapiens (human)	2	3
P54756	Ephrin type-A receptor 5	EPHA5 BSK EHK1 HEK7 TYRO4	Homo sapiens (human)	8	3
Q96B86	Repulsive guidance molecule A	RGMA RGM	Homo sapiens (human)	4	3	Mycobacterium avium complex disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease basal cell carcinoma breast cancer bronchiectasis cancer chronic fatigue syndrome chronic kidney disease complex partial epilepsy cone-rod dystrophy 2 cone-rod dystrophy cystic fibrosis disease of mental health embryoma encephalitis encephalomyelitis epilepsy hemochromatosis type 2 hemochromatosis type 2A hemochromatosis heroin dependence lesion of sciatic nerve lung disease middle cerebral artery infarction morphine dependence multiple sclerosis myelitis neuromyelitis optica obesity opiate dependence primary progressive multiple sclerosis progressive relapsing multiple sclerosis prostate cancer prostate carcinoma psychotic disorder sciatic neuropathy secondary progressive multiple sclerosis temporal lobe epilepsy visual epilepsy
Q15198	Platelet-derived growth factor receptor-like protein	PDGFRL PRLTS	Homo sapiens (human)	2	3
Q6U841	Sodium-driven chloride bicarbonate exchanger	SLC4A10 NBCN2 NCBE	Homo sapiens (human)	4	3
Q3UVC0	Kinase suppressor of Ras 2	Ksr2	Mus musculus (house mouse)	3	3
Q61464	Zinc finger protein 638	Znf638 Np220 Zfml Zfp638	Mus musculus (house mouse)	2	3
Q96FE5	Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1	LINGO1 LERN1 LRRN6A	Homo sapiens (human)	10	3
O43505	Beta-1,4-glucuronyltransferase 1	B4GAT1 B3GNT1 B3GNT6	Homo sapiens (human)	2	3	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome anencephaly 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 blindness breast cancer breast carcinoma cataract centronuclear myopathy coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy-dystroglycanopathy type A13 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy facioscapulohumeral muscular dystrophy glaucoma hydranencephaly hydrocephalus hydronephrosis isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lissencephaly megaconial type congenital muscular dystrophy microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 nemaline myopathy 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 optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rigid spine muscular dystrophy 1 rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type
Q8BM75	AT-rich interactive domain-containing protein 5B	Arid5b Desrt Mrf2	Mus musculus (house mouse)	3	3
Q00987	E3 ubiquitin-protein ligase Mdm2	MDM2	Homo sapiens (human)	1	3
Q6PDI5	Proteasome adapter and scaffold protein ECM29	Ecpas Ecm29 Kiaa0368	Mus musculus (house mouse)	1	3
P14046	Alpha-1-inhibitor 3	A1i3	Rattus norvegicus (Norway rat)	13	3

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