GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of GlyTouCan IDs	Disease Ontology
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
Q14190	Single-minded homolog 2	SIM2 BHLHE15	1
Q9NZU5	LIM and cysteine-rich domains protein 1	LMCD1	1
P17025	Zinc finger protein 182	ZNF182 KOX14 ZNF21	1
P26639	Threonine--tRNA ligase 1, cytoplasmic	TARS1 TARS	1
Q63HM1	Kynurenine formamidase	AFMID	1	colon cancer colonic benign neoplasm colorectal cancer large intestine cancer
P17017	Zinc finger protein 14	ZNF14 GIOT4 KOX6	1
Q9NZR4	Visual system homeobox 1	VSX1 RINX	1
Q9NR50	Translation initiation factor eIF2B subunit gamma	EIF2B3	1
Q13686	Nucleic acid dioxygenase ALKBH1	ALKBH1 ABH ABH1 ALKBH	1
Q14320	Protein FAM50A	FAM50A DXS9928E HXC26 XAP5	1
Q99436	Proteasome subunit beta type-7	PSMB7 Z	1
Q9NQ88	Fructose-2,6-bisphosphatase TIGAR	TIGAR C12orf5	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Fanconi anemia complementation group A Fanconi anemia Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute pancreatitis adult T-cell leukemia/lymphoma adult lymphoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood leukemia childhood lymphoma chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma cleft palate collecting duct carcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma degenerative disc disease dementia embryoma epilepsy esophagus squamous cell carcinoma familial retinoblastoma giant cell glioblastoma glioblastoma gliosarcoma hemiplegia hepatocellular carcinoma high grade glioma hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer isolated cleft palate large intestine cancer lateral sclerosis leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma mixed glioma motor neuron disease nasopharynx carcinoma neurodegenerative disease nonpapillary renal cell carcinoma obesity obsolete ymphosarcoma pancreatitis papillary renal cell carcinoma primary cutaneous T-cell non-Hodgkin lymphoma renal carcinoma renal cell carcinoma retinoblastoma sarcomatoid renal cell carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy stomach cancer stomach carcinoma trilateral retinoblastoma ulcerative colitis
Q9NT62	Ubiquitin-like-conjugating enzyme ATG3	ATG3 APG3 APG3L	1
Q7RTT6	Putative protein SSX6	SSX6P SSX6	1
Q96S59	Ran-binding protein 9	RANBP9 RANBPM	1
Q92785	Zinc finger protein ubi-d4	DPF2 BAF45D REQ UBID4	1
Q9Y224	RNA transcription, translation and transport factor protein	RTRAF C14orf166	1
Q9H6Y2	WD repeat-containing protein 55	WDR55	1
Q5T1V6	Probable ATP-dependent RNA helicase DDX59	DDX59 ZNHIT5	1
P82663	Small ribosomal subunit protein mS25	MRPS25 RPMS25	1

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