GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **16051 - 16075** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q8NDH2	Leucine-rich repeat transmembrane protein CCDC168	CCDC168 C13orf40	Homo sapiens (human)	1	1
Q8NDF8	Terminal nucleotidyltransferase 4B	TENT4B GLD4 PAPD5 TRF4-2 TUT3	Homo sapiens (human)	0	1
Q8NDD1	Uncharacterized protein C1orf131	C1orf131 cPERP-A	Homo sapiens (human)	4	2
Q8NDC0	MAPK-interacting and spindle-stabilizing protein-like	MAPK1IP1L C14orf32	Homo sapiens (human)	10	2
Q8NDA8	Maestro heat-like repeat-containing protein family member 1	MROH1 HEATR7A KIAA1833	Homo sapiens (human)	0	1
Q8NDA2	Hemicentin-2	HMCN2	Homo sapiens (human)	44	26
Q8ND94	LRRN4 C-terminal-like protein	LRRN4CL	Homo sapiens (human)	1	0
Q8ND83	SLAIN motif-containing protein 1	SLAIN1 C13orf32	Homo sapiens (human)	11	2
Q8ND82	Zinc finger protein 280C	ZNF280C SUHW3 ZNF633	Homo sapiens (human)	1	2
Q8ND71	GTPase IMAP family member 8	GIMAP8 IAN9 IANT	Homo sapiens (human)	0	1
Q8ND61	Uncharacterized protein C3orf20	C3orf20	Homo sapiens (human)	0	1
Q8ND56	Protein LSM14 homolog A	LSM14A C19orf13 FAM61A RAP55 RAP55A	Homo sapiens (human)	4	1
Q8ND30	Liprin-beta-2	PPFIBP2	Homo sapiens (human)	0	1
Q8ND24	RING finger protein 214	RNF214	Homo sapiens (human)	2	1
Q8ND18	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase (Fragment)	DKFZp547E046	Homo sapiens (human)	1	0
Q8ND07	Basal body-orientation factor 1	BBOF1 C14orf45 CCDC176	Homo sapiens (human)	0	1
Q8ND04	Nonsense-mediated mRNA decay factor SMG8	SMG8 ABC2 C17orf71	Homo sapiens (human)	1	1
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
Q8NCW5	NAD(P)H-hydrate epimerase	NAXE AIBP APOA1BP YJEFN1	Homo sapiens (human)	2	2
Q8NCW0	Kremen protein 2	KREMEN2 KRM2	Homo sapiens (human)	5	1
Q8NCT3	Putative tyrosine carboxypeptidase MATCAP2	MATCAP2 KIAA0895	Homo sapiens (human)	1	1
Q8NCS7	Choline transporter-like protein 5	SLC44A5 CTL5	Homo sapiens (human)	3	0
Q8NCR9	Clarin-3	CLRN3 TMEM12 USH3AL1	Homo sapiens (human)	1	0
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
Q8NCN5	Pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial	PDPR KIAA1990	Homo sapiens (human)	0	1

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