GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9H5K3	Protein O-mannose kinase	POMK SGK196	5	9	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert 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 cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 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 ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
Q9H5J4	Very long chain fatty acid elongase 6	ELOVL6 FACE LCE	2	2	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
Q9H5I5	Piezo-type mechanosensitive ion channel component 2	PIEZO2 C18orf30 C18orf58 FAM38B	7	4
Q9H5I1	Histone-lysine N-methyltransferase SUV39H2	SUV39H2 KMT1B	0	1
Q9H598	Vesicular inhibitory amino acid transporter	SLC32A1 VGAT VIAAT	1	1
Q9H583	HEAT repeat-containing protein 1	HEATR1 BAP28 UTP10	1	2
Q9H582	Zinc finger protein 644	ZNF644 KIAA1221 ZEP2	3	1
Q9H579	Protein MROH8	MROH8 C20orf131 C20orf132	0	1
Q9H501	ESF1 homolog	ESF1 ABTAP C20orf6	0	1
Q9H4Z2	Zinc finger protein 335	ZNF335	1	1
Q9H4S2	GS homeobox 1	GSX1 GSH1	1	1
Q9H4R4	Putative nuclear receptor corepressor 1-like protein NCOR1P1	NCOR1P1 C20orf191	0	1
Q9H4Q4	PR domain zinc finger protein 12	PRDM12 PFM9	0	1
Q9H4M9	EH domain-containing protein 1	EHD1 PAST PAST1	0	1
Q9H4L7	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1	SMARCAD1 KIAA1122	0	1
Q9H4L4	Sentrin-specific protease 3	SENP3 SSP3 SUSP3	0	1
Q9H4K1	RIB43A-like with coiled-coils protein 2	RIBC2 C22orf11	0	1
Q9H4I9	Essential MCU regulator, mitochondrial	SMDT1 C22orf32 EMRE	1	1
Q9H4I3	TraB domain-containing protein	TRABD TTG2	0	1
Q9H4I2	Zinc fingers and homeoboxes protein 3	ZHX3 KIAA0395 TIX1	14	1
Q9H4H8	Protein FAM83D	FAM83D C20orf129	1	2
Q9H4G1	Cystatin-9-like	CST9L CTES7B	2	0
Q9H4G0	Band 4.1-like protein 1	EPB41L1 KIAA0338	12	1
Q9H4F8	SPARC-related modular calcium-binding protein 1	SMOC1	17	9
Q9H4F1	Alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase	ST6GALNAC4 SIAT3C SIAT7D	5	3	Guillain-Barre syndrome Miller Fisher syndrome cancer thyroid gland follicular carcinoma

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