GlyCosmos Portal

Displaying entries **6126 - 6150** of **18496** in total

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q6Y2X3	DnaJ homolog subfamily C member 14	DNAJC14 DRIP78 HDJ3	1	1
Q6Y288	Beta-1,3-glucosyltransferase	B3GLCT B3GALTL B3GTL	3	6	Axenfeld-Rieger syndrome IGSF1 deficiency syndrome Klippel-Feil syndrome Kuhnt-Junius degeneration Meckel syndrome Peters anomaly Peters plus syndrome Tn polyagglutination syndrome age related macular degeneration anemia 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 autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease blindness cataract cerebral degeneration cleft lip cleft palate coloboma communicating hydrocephalus congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nystagmus congenital ptosis cornea plana craniosynostosis cryptorchidism degeneration of macula and posterior pole depressive disorder dissociated nystagmus epilepsy eye disease glaucoma heart septal defect hydrocephalus hydronephrosis hypoplastic left heart syndrome hypospadias hypothyroidism imperforate anus inguinal hernia intellectual disability isolated cleft palate learning disability macrocytic anemia macular degeneration major depressive disorder melancholic depression microcephaly myopia myxedema obsolete melancholia obstructive hydrocephalus omphalocele optic atrophy patent ductus arteriosus patent foramen ovale pathologic nystagmus placental insufficiency polyhydramnios popliteal pterygium syndrome ptosis pulmonary valve stenosis recurrent corneal erosion renal hypoplasia scoliosis senile degeneration of brain sensorineural hearing loss spina bifida occulta spondylolisthesis spontaneous ocular nystagmus syndactyly trichohepatoenteric syndrome 1 trichohepatoenteric syndrome umbilical hernia ventricular septal defect visual epilepsy
Q6Y1H2	Very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 2	HACD2 PTPLB	1	1
Q6XZF7	Dynamin-binding protein	DNMBP ARHGEF36 KIAA1010 TUBA	1	1
Q6XZB0	Lipase member I	LIPI LPDL	2	0
Q6XUX3	Dual serine/threonine and tyrosine protein kinase	DSTYK KIAA0472 RIP5 RIPK5 SGK496	1	1
Q6XPR3	Repetin	RPTN	2	1
Q6XE24	RNA-binding motif, single-stranded-interacting protein 3	RBMS3	0	1
Q6X907	Neuropilin	NRP1	2	0
Q6X784	Zona pellucida-binding protein 2	ZPBP2 ZPBPL	4	0
Q6X4W1	NMDA receptor synaptonuclear signaling and neuronal migration factor	NSMF NELF	1	1
Q6X4U4	Sclerostin domain-containing protein 1	SOSTDC1 USAG1	2	9
Q6WRX3	Protein zyg-11 homolog A	ZYG11A ZYG11	1	1
Q6WRI0	Immunoglobulin superfamily member 10	IGSF10 CMF608	21	8
Q6WN34	Chordin-like protein 2	CHRDL2 BNF1 CHL2	11	29
Q6WKZ4	Rab11 family-interacting protein 1	RAB11FIP1 RCP	0	1
Q6WCQ1	Myosin phosphatase Rho-interacting protein	MPRIP KIAA0864 MRIP RHOIP3	5	2
Q6W5P4	Neuropeptide S receptor	NPSR1 GPR154 GPRA PGR14	1	0
Q6W4X9	Mucin-6	MUC6	9	10
Q6W3E5	Glycerophosphodiester phosphodiesterase domain-containing protein 4	GDPD4 GDE6 UGPQ	2	0
Q6W2J9	BCL-6 corepressor	BCOR KIAA1575	12	1
Q6VY07	Phosphofurin acidic cluster sorting protein 1	PACS1 KIAA1175	3	1
Q6VVB1	E3 ubiquitin-protein ligase NHLRC1	NHLRC1 EPM2B	1	1
Q6VS58	MHC class I antigen (Fragment)	HLA-B	1	0
Q6VN20	Ran-binding protein 10	RANBP10 KIAA1464	1	2

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