GlyCosmos Portal

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Displaying entries **10076 - 10100** 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
Q8NEZ3	WD repeat-containing protein 19	WDR19 IFT144 KIAA1638	Homo sapiens (human)	0	1
Q865S1	AP-3 complex subunit delta-1	AP3D1 BLVR	Bos taurus (cattle)	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
Q4CZR0	Small GTP-binding protein Rab1, putative	Tc00.1047053503715.30	Trypanosoma cruzi strain CL Brener	0	1
Q91V64	Isochorismatase domain-containing protein 1	Isoc1	Mus musculus (house mouse)	0	1
P51149	Ras-related protein Rab-7a	RAB7A RAB7	Homo sapiens (human)	1	1
Q4CYC6	Uncharacterized protein	Tc00.1047053510679.40	Trypanosoma cruzi strain CL Brener	0	1
P56392	Cytochrome c oxidase subunit 7A1, mitochondrial	Cox7a1 Cox7a Cox7ah	Mus musculus (house mouse)	0	1
Q8CDJ8	Stonin-1	Ston1 Salf Sblf Stn1	Mus musculus (house mouse)	0	1
K2N6V1	HECT domain-containing protein	MOQ_002480	Trypanosoma cruzi marinkellei	0	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
Q64339	Ubiquitin-like protein ISG15	Isg15 G1p2 Ucrp	Mus musculus (house mouse)	0	1
Q4E617	Uncharacterized protein	Tc00.1047053508153.760	Trypanosoma cruzi strain CL Brener	0	1
Q12972	Nuclear inhibitor of protein phosphatase 1	PPP1R8 ARD1 NIPP1	Homo sapiens (human)	1	1
Q9SU99	HnRNP-like protein	At4g26650	Arabidopsis thaliana (thale cress)	0	1
B3KNS4	Endogenous retrovirus group K3 member 1	ERVK3-1	Homo sapiens (human)	0	1
P26684	Endothelin-1 receptor	Ednra	Rattus norvegicus (Norway rat)	2	1
Q9BW19	Kinesin-like protein KIFC1	KIFC1 HSET KNSL2	Homo sapiens (human)	0	1
Q4DXX0	Trichohyalin	Tc00.1047053510431.240	Trypanosoma cruzi strain CL Brener	0	1
Q9NZ56	Formin-2	FMN2	Homo sapiens (human)	0	1

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