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

« First

‹ Prev

…

590

591

592

593

594

595

596

597

598

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q6UVW9	C-type lectin domain family 2 member A	CLEC2A KACL	Homo sapiens (human)	3	0
P05090	Apolipoprotein D	APOD	Homo sapiens (human)	3	217
A0A0S2Z5C8	Metal cation symporter ZIP14	SLC39A14	Homo sapiens (human)	3	0
P62937	Peptidyl-prolyl cis-trans isomerase A	PPIA CYPA	Homo sapiens (human)	3	8
Q7L8C5	Synaptotagmin-13	SYT13 KIAA1427	Homo sapiens (human)	3	3
W8RL45	MHC class I chain-related protein A (Fragment)	MICA	Homo sapiens (human)	3	0
P29972	Aquaporin-1	AQP1 CHIP28	Homo sapiens (human)	3	1
A0A7I2V3C1	ADAM metallopeptidase domain 9	ADAM9	Homo sapiens (human)	3	0
P32245	Melanocortin receptor 4	MC4R	Homo sapiens (human)	3	0
Q13361	Microfibrillar-associated protein 5	MFAP5 MAGP2	Homo sapiens (human)	3	36
P21796	Voltage-dependent anion-selective channel protein 1	VDAC1 VDAC	Homo sapiens (human)	3	3
F5CA56	Major histocompatibility complex class I chain-related protein A (Fragment)	MICA	Homo sapiens (human)	3	0
Q8WWT9	Na(+)/dicarboxylate cotransporter 3	SLC13A3 NADC3 SDCT2	Homo sapiens (human)	3	1
V5P5H4	MHC class I polypeptide-related protein A (Fragment)	MICA	Homo sapiens (human)	3	0
O15371	Eukaryotic translation initiation factor 3 subunit D	EIF3D EIF3S7	Homo sapiens (human)	3	1
Q6S8J3	POTE ankyrin domain family member E	POTEE A26C1A POTE2	Homo sapiens (human)	3	2
Q14160	Protein scribble homolog	SCRIB CRIB1 KIAA0147 LAP4 SCRB1 VARTUL	Homo sapiens (human)	3	2
O75631	Uroplakin-3a	UPK3A UPK3	Homo sapiens (human)	3	0
B4E1C2	Kininogen 1, isoform CRA_b	KNG1	Homo sapiens (human)	3	0
Q13023	A-kinase anchor protein 6	AKAP6 AKAP100 KIAA0311	Homo sapiens (human)	3	1
Q9P1A6	Disks large-associated protein 2	DLGAP2 C8orf68 DAP2 ERICH1-AS1	Homo sapiens (human)	3	3
P31947	14-3-3 protein sigma	SFN HME1	Homo sapiens (human)	3	2
A0A0S2Z5Z7	Metal cation symporter ZIP14 (Fragment)	SLC39A14	Homo sapiens (human)	3	0
P48067	Sodium- and chloride-dependent glycine transporter 1	SLC6A9	Homo sapiens (human)	3	2
Q6Y288	Beta-1,3-glucosyltransferase	B3GLCT B3GALTL B3GTL	Homo sapiens (human)	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

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements