GlyCosmos Portal

Displaying entries **15951 - 15975** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
P14735	Insulin-degrading enzyme	IDE	1
Q5H9T9	Fibrous sheath CABYR-binding protein	FSCB C14orf155	1
O94952	F-box only protein 21	FBXO21 FBX21 KIAA0875	1
Q15007	Pre-mRNA-splicing regulator WTAP	WTAP KIAA0105	1
Q96HJ9	Protein FMC1 homolog	FMC1 C7orf55	1
Q8WVX3	Uncharacterized protein C4orf3	C4orf3	1
P83731	Large ribosomal subunit protein eL24	RPL24	1
O43598	5-hydroxymethyl-dUMP N-hydrolase	DNPH1 C6orf108 RCL	1
P55769	NHP2-like protein 1	SNU13 NHP2L1	1
Q7Z5J8	Ankyrin and armadillo repeat-containing protein	ANKAR	1
Q8TF05	Serine/threonine-protein phosphatase 4 regulatory subunit 1	PPP4R1 MEG1 PP4R1	1
Q8TBX8	Phosphatidylinositol 5-phosphate 4-kinase type-2 gamma	PIP4K2C PIP5K2C	1	bipolar disorder breast cancer cancer diabetic ketoacidosis embryoma lingual-facial-buccal dyskinesia obsolete type 1 diabetes mellitus 9 schizophrenia type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
P07099	Epoxide hydrolase 1	EPHX1 EPHX EPOX	1
P00367	Glutamate dehydrogenase 1, mitochondrial	GLUD1 GLUD	1
Q9Y3C6	Peptidyl-prolyl cis-trans isomerase-like 1	PPIL1 CYPL1	1
P16930	Fumarylacetoacetase	FAH	1
Q6ZU67	BEN domain-containing protein 4	BEND4 CCDC4	1
O95070	Protein YIF1A	YIF1A 54TM HYIF1P YIF1	1
Q8NEZ3	WD repeat-containing protein 19	WDR19 IFT144 KIAA1638	1
P29083	General transcription factor IIE subunit 1	GTF2E1 TF2E1	1
Q9Y5P6	Mannose-1-phosphate guanyltransferase beta	GMPPB	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
Q9BRT2	Ubiquinol-cytochrome c reductase complex assembly factor 2	UQCC2 C6orf125 MNF1	1
B3KNS4	Endogenous retrovirus group K3 member 1	ERVK3-1	1
Q9BW19	Kinesin-like protein KIFC1	KIFC1 HSET KNSL2	1
Q9NZ56	Formin-2	FMN2	1

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