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 **5226 - 5250** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9BY21	G-protein coupled receptor 87	GPR87 GPR95	Homo sapiens (human)	4	1
Q9Y5G6	Protocadherin gamma-A7	PCDHGA7	Homo sapiens (human)	2	1
O75121	Microfibrillar-associated protein 3-like	MFAP3L KIAA0626	Homo sapiens (human)	5	1
Q6ZU67	BEN domain-containing protein 4	BEND4 CCDC4	Homo sapiens (human)	0	1
Q13148	TAR DNA-binding protein 43	TARDBP TDP43	Homo sapiens (human)	3	1
O95070	Protein YIF1A	YIF1A 54TM HYIF1P YIF1	Homo sapiens (human)	0	1
Q7Z5P9	Mucin-19	MUC19	Homo sapiens (human)	14	1
Q8NEZ3	WD repeat-containing protein 19	WDR19 IFT144 KIAA1638	Homo sapiens (human)	0	1
P00519	Tyrosine-protein kinase ABL1	ABL1 ABL JTK7	Homo sapiens (human)	3	1
P29083	General transcription factor IIE subunit 1	GTF2E1 TF2E1	Homo sapiens (human)	0	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
P51149	Ras-related protein Rab-7a	RAB7A RAB7	Homo sapiens (human)	1	1
Q02643	Growth hormone-releasing hormone receptor	GHRHR	Homo sapiens (human)	1	1
Q6P2Q9	Pre-mRNA-processing-splicing factor 8	PRPF8 PRPC8	Homo sapiens (human)	3	1
Q9BRT2	Ubiquinol-cytochrome c reductase complex assembly factor 2	UQCC2 C6orf125 MNF1	Homo sapiens (human)	0	1
Q9UQ88	Cyclin-dependent kinase 11A	CDK11A CDC2L2 CDC2L3 PITSLREB	Homo sapiens (human)	1	1
Q12972	Nuclear inhibitor of protein phosphatase 1	PPP1R8 ARD1 NIPP1	Homo sapiens (human)	1	1
B3KNS4	Endogenous retrovirus group K3 member 1	ERVK3-1	Homo sapiens (human)	0	1
Q9BW19	Kinesin-like protein KIFC1	KIFC1 HSET KNSL2	Homo sapiens (human)	0	1
Q9NZ56	Formin-2	FMN2	Homo sapiens (human)	0	1
Q14190	Single-minded homolog 2	SIM2 BHLHE15	Homo sapiens (human)	0	1
Q05519	Serine/arginine-rich splicing factor 11	SRSF11 SFRS11	Homo sapiens (human)	5	1
Q9NZU5	LIM and cysteine-rich domains protein 1	LMCD1	Homo sapiens (human)	0	1
P17025	Zinc finger protein 182	ZNF182 KOX14 ZNF21	Homo sapiens (human)	0	1
Q13227	G protein pathway suppressor 2	GPS2	Homo sapiens (human)	1	1

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