GlyCosmos Portal

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Displaying entries **114376 - 114400** 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
Q95207	Interferon alpha/beta receptor 2	IFNAR2 IFNARB	Ovis aries (sheep)	5	0
Q99NG0	Helicase ARIP4	Rad54l2 Arip4 Srisnf2l	Mus musculus (house mouse)	5	1
P14075	Envelope glycoprotein gp62	env	Human T-cell lymphotrophic virus type 1 (Caribbean isolate)	5	0
P03383	Envelope glycoprotein gp63	env	Human T-lymphotropic virus 2	5	0
Q3E884	Putative L-type lectin-domain containing receptor kinase I.10	LECRK110	Arabidopsis thaliana (thale cress)	5	0
Q0D5R3	Cysteine-rich receptor-like protein kinase 6	CRK6	Oryza sativa Japonica Group (Japanese rice)	5	0
Q75K78	Cytokinin dehydrogenase 9	CKX9	Oryza sativa Japonica Group (Japanese rice)	5	0
Q0CRX0	Tyrosinase P	tyrP melB	Aspergillus terreus NIH2624	5	0
O75629	Protein CREG1	CREG1 CREG	Homo sapiens (human)	5	54
O14498	Immunoglobulin superfamily containing leucine-rich repeat protein	ISLR	Homo sapiens (human)	5	22
Q9Y6A1	Protein O-mannosyl-transferase 1	POMT1	Homo sapiens (human)	5	8	Axenfeld-Rieger syndrome Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Marfan 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 brain cancer brain disease buphthalmos campomelic dysplasia cardiomyopathy cataract centronuclear myopathy cleft lip cleft palate clubfoot coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy 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 A1 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fibromyalgia fundus albipunctatus fundus dystrophy glaucoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertrophic cardiomyopathy hypertropia imperforate anus intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly locked-in syndrome mechanical strabismus megaconial type congenital muscular dystrophy megalocornea meningocele 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 myopathy myopia myositis nemaline myopathy neuromuscular disease 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 peripheral retinal degeneration placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 quadriplegia recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type tuberous sclerosis visual epilepsy
Q13315	Serine-protein kinase ATM	ATM	Homo sapiens (human)	5	2
O97467	Hexose transporter 1	ht1	Plasmodium falciparum (malaria parasite P. falciparum)	5	0
Q6QNF4	Hepatocyte growth factor activator	HGFAC	Canis lupus familiaris (dog)	5	0
B5BQV3	Neurotrophic tyrosine kinase receptor, type2, splicing variant T3 alpha	Ntrk2 ntrk2	Mus musculus (house mouse)	5	0
Q5DRD5	Protocadherin beta-14	PCDHB14	Pan troglodytes (chimpanzee)	5	0
Q8LDW6	Endonuclease 3	ENDO3	Arabidopsis thaliana (thale cress)	5	0
Q62283	Tetraspanin-7	Tspan7 Mxs1 Tm4sf2	Mus musculus (house mouse)	5	0
A0A6P5L480	Angiotensin-converting enzyme	LOC110215741	Phascolarctos cinereus (koala)	5	0
P52823	Stanniocalcin-1	STC1 STC	Homo sapiens (human)	5	1
Q5BFG8	Beta-glucosidase B	bglB	Aspergillus nidulans FGSC A4	5	0
Q62638	Golgi apparatus protein 1	Glg1 Esl1 Mg160	Rattus norvegicus (Norway rat)	5	0
E9PGC5	protein-tyrosine-phosphatase	PTPRK	Homo sapiens (human)	5	0
Q4W9C7	ABC multidrug transporter G	abcG	Aspergillus fumigatus Af293	5	0
P09344	Hemagglutinin	HA	Influenza A virus (A/starling/Victoria/5156/1985(H7N7))	5	0

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