GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **13701 - 13725** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8NCH0	Carbohydrate sulfotransferase 14	CHST14 D4ST1	Homo sapiens (human)	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
Q8NCI6	Beta-galactosidase-1-like protein 3	GLB1L3	Homo sapiens (human)	0	1
Q8NCL4	Polypeptide N-acetylgalactosaminyltransferase 6	GALNT6	Homo sapiens (human)	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
Q8NCL9	Protein APCDD1-like	APCDD1L	Homo sapiens (human)	1	0
Q8NCM2	Potassium voltage-gated channel subfamily H member 5	KCNH5 EAG2	Homo sapiens (human)	2	1
Q8NCM8	Cytoplasmic dynein 2 heavy chain 1	DYNC2H1 DHC1B DHC2 DNCH2 DYH1B KIAA1997	Homo sapiens (human)	3	4
Q8NCN4	E3 ubiquitin-protein ligase RNF169	RNF169 KIAA1991	Homo sapiens (human)	0	1
Q8NCN5	Pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial	PDPR KIAA1990	Homo sapiens (human)	0	1
Q8NCR0	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2	Homo sapiens (human)	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
Q8NCR9	Clarin-3	CLRN3 TMEM12 USH3AL1	Homo sapiens (human)	1	0
Q8NCS7	Choline transporter-like protein 5	SLC44A5 CTL5	Homo sapiens (human)	3	0
Q8NCT3	Putative tyrosine carboxypeptidase MATCAP2	MATCAP2 KIAA0895	Homo sapiens (human)	1	1
Q8NCW0	Kremen protein 2	KREMEN2 KRM2	Homo sapiens (human)	5	1
Q8NCW5	NAD(P)H-hydrate epimerase	NAXE AIBP APOA1BP YJEFN1	Homo sapiens (human)	2	2
Q8NCW6	Polypeptide N-acetylgalactosaminyltransferase 11	GALNT11	Homo sapiens (human)	2	5	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
Q8ND04	Nonsense-mediated mRNA decay factor SMG8	SMG8 ABC2 C17orf71	Homo sapiens (human)	1	1
Q8ND07	Basal body-orientation factor 1	BBOF1 C14orf45 CCDC176	Homo sapiens (human)	0	1
Q8ND18	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	DKFZp547E046	Homo sapiens (human)	1	0
Q8ND24	RING finger protein 214	RNF214	Homo sapiens (human)	2	1
Q8ND30	Liprin-beta-2	PPFIBP2	Homo sapiens (human)	0	1
Q8ND56	Protein LSM14 homolog A	LSM14A C19orf13 FAM61A RAP55 RAP55A	Homo sapiens (human)	4	1
Q8ND61	Uncharacterized protein C3orf20	C3orf20	Homo sapiens (human)	0	1
Q8ND71	GTPase IMAP family member 8	GIMAP8 IAN9 IANT	Homo sapiens (human)	0	1
Q8ND82	Zinc finger protein 280C	ZNF280C SUHW3 ZNF633	Homo sapiens (human)	1	2
Q8ND83	SLAIN motif-containing protein 1	SLAIN1 C13orf32	Homo sapiens (human)	11	2

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