GlyCosmos Portal

Displaying entries **14826 - 14850** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q6UVW9	C-type lectin domain family 2 member A	CLEC2A KACL	3	0
P05090	Apolipoprotein D	APOD	3	217
A0A0S2Z5C8	Metal cation symporter ZIP14	SLC39A14	3	0
P62937	Peptidyl-prolyl cis-trans isomerase A	PPIA CYPA	3	8
Q7L8C5	Synaptotagmin-13	SYT13 KIAA1427	3	3
W8RL45	MHC class I chain-related protein A (Fragment)	MICA	3	0
P29972	Aquaporin-1	AQP1 CHIP28	3	1
A0A7I2V3C1	ADAM metallopeptidase domain 9	ADAM9	3	0
P32245	Melanocortin receptor 4	MC4R	3	0
Q13361	Microfibrillar-associated protein 5	MFAP5 MAGP2	3	36
P21796	Voltage-dependent anion-selective channel protein 1	VDAC1 VDAC	3	3
F5CA56	Major histocompatibility complex class I chain-related protein A (Fragment)	MICA	3	0
Q8WWT9	Na(+)/dicarboxylate cotransporter 3	SLC13A3 NADC3 SDCT2	3	1
V5P5H4	MHC class I polypeptide-related protein A (Fragment)	MICA	3	0
O15371	Eukaryotic translation initiation factor 3 subunit D	EIF3D EIF3S7	3	1
Q6S8J3	POTE ankyrin domain family member E	POTEE A26C1A POTE2	3	2
Q14160	Protein scribble homolog	SCRIB CRIB1 KIAA0147 LAP4 SCRB1 VARTUL	3	2
O75631	Uroplakin-3a	UPK3A UPK3	3	0
B4E1C2	Kininogen 1, isoform CRA_b	KNG1	3	0
Q13023	A-kinase anchor protein 6	AKAP6 AKAP100 KIAA0311	3	1
Q9P1A6	Disks large-associated protein 2	DLGAP2 C8orf68 DAP2 ERICH1-AS1	3	3
P31947	14-3-3 protein sigma	SFN HME1	3	2
A0A0S2Z5Z7	Metal cation symporter ZIP14 (Fragment)	SLC39A14	3	0
P48067	Sodium- and chloride-dependent glycine transporter 1	SLC6A9	3	2
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

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