GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8ND56	Protein LSM14 homolog A	LSM14A C19orf13 FAM61A RAP55 RAP55A	4	1
Q8ND30	Liprin-beta-2	PPFIBP2	0	1
Q8ND24	RING finger protein 214	RNF214	2	1
Q8ND18	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	DKFZp547E046	1	0
Q8ND07	Basal body-orientation factor 1	BBOF1 C14orf45 CCDC176	0	1
Q8ND04	Nonsense-mediated mRNA decay factor SMG8	SMG8 ABC2 C17orf71	1	1
Q8NCW6	Polypeptide N-acetylgalactosaminyltransferase 11	GALNT11	2	5	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
Q8NCW5	NAD(P)H-hydrate epimerase	NAXE AIBP APOA1BP YJEFN1	2	2
Q8NCW0	Kremen protein 2	KREMEN2 KRM2	5	1
Q8NCT3	Putative tyrosine carboxypeptidase MATCAP2	MATCAP2 KIAA0895	1	1
Q8NCS7	Choline transporter-like protein 5	SLC44A5 CTL5	3	0
Q8NCR9	Clarin-3	CLRN3 TMEM12 USH3AL1	1	0
Q8NCR0	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2	2	0	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 breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder 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 obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
Q8NCN5	Pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial	PDPR KIAA1990	0	1
Q8NCN4	E3 ubiquitin-protein ligase RNF169	RNF169 KIAA1991	0	1
Q8NCM8	Cytoplasmic dynein 2 heavy chain 1	DYNC2H1 DHC1B DHC2 DNCH2 DYH1B KIAA1997	3	4
Q8NCM2	Potassium voltage-gated channel subfamily H member 5	KCNH5 EAG2	2	1
Q8NCL9	Protein APCDD1-like	APCDD1L	1	0
Q8NCL4	Polypeptide N-acetylgalactosaminyltransferase 6	GALNT6	8	1	adenocarcinoma adenoma breast cancer breast carcinoma cancer carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis granular cell carcinoma large intestine cancer lung adenocarcinoma lung cancer ovarian cancer ovarian carcinoma sarcomatoid carcinoma serous cystadenocarcinoma stomach cancer stomach carcinoma tubular adenocarcinoma uterine corpus cancer
Q8NCI6	Beta-galactosidase-1-like protein 3	GLB1L3	0	1
Q8NCH0	Carbohydrate sulfotransferase 14	CHST14 D4ST1	6	4	Ehlers-Danlos syndrome musculocontractural type 1 Ehlers-Danlos syndrome Marfan syndrome Peters anomaly agnosia arthropathy atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect brittle cornea syndrome 1 cleft palate clubfoot congenital diaphragmatic hernia cornea plana craniosynostosis cryptorchidism developmental coordination disorder distal arthrogryposis familial nephrotic syndrome familial periodic paralysis glaucoma hiatus hernia hydrocephalus hydronephrosis hypertropia isolated cleft palate lipoid nephrosis mechanical strabismus myopathy myopia nephrotic syndrome obsolete constipation omphalocele ophthalmoplegia osteogenesis imperfecta patent foramen ovale pneumothorax prostate cancer prostate carcinoma retinal detachment scoliosis sensorineural hearing loss situs inversus strabismus tuberous sclerosis umbilical hernia
Q8NCG5	Carbohydrate sulfotransferase 4	CHST4	3	0	arthritis arthropathy cancer colitis colon cancer colon carcinoma colon mucinous adenocarcinoma colonic benign neoplasm colorectal cancer gastroenteritis ileitis ileocolitis large intestine cancer osteoarthritis
Q8NCF5	NFATC2-interacting protein	NFATC2IP NIP45	1	1
Q8NCF0	C-type lectin domain family 18 member C	CLEC18C MRLP3	1	0
Q8NCE2	Myotubularin-related protein 14	MTMR14 C3orf29	2	0	Bell's palsy agnosia asphyxia neonatorum autosomal dominant centronuclear myopathy autosomal recessive centronuclear myopathy cancer capillary hemangioma cardiomyopathy cavernous hemangioma centronuclear myopathy 1 centronuclear myopathy X-linked centronuclear myopathy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder endomyocardial fibrosis facial nerve disease facial paralysis familial periodic paralysis hemangioma hepatocellular carcinoma hypertrophic cardiomyopathy liver cancer liver carcinoma malignant hyperthermia megaconial type congenital muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy obesity ophthalmoplegia ovarian carcinoma polyhydramnios ptosis rigid spine muscular dystrophy 1 tubular aggregate myopathy 1

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