GlyCosmos Portal

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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 **107476 - 107500** 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
O75631	Uroplakin-3a	UPK3A UPK3	Homo sapiens (human)	3	0
G2PZJ2	GMC oxidoreductase-like protein	MYCTH_2299749	Thermothelomyces thermophilus ATCC 42464	3	0
B4E1C2	Kininogen 1, isoform CRA_b	KNG1	Homo sapiens (human)	3	0
Q5XGR4	TM2 domain-containing protein 2	tm2d2	Xenopus laevis (African clawed frog)	3	0
Q9ER58	Testican-2	Spock2 Ticn2	Mus musculus (house mouse)	3	8
Q59VL7	Putative alpha-1,3-mannosyltransferase MNN15	MNN15	Candida albicans SC5314	3	0
Q9FX01	3beta-hydroxysteroid-dehydrogenase/decarboxylase isoform 1	3BETAHSD/D1 RTNLB24	Arabidopsis thaliana (thale cress)	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
S4UJD1	Hemagglutinin-neuraminidase	HN	Mammalian orthorubulavirus 5	3	0
Q5ZL18	N-fatty-acyl-amino acid synthase/hydrolase PM20D1	PM20D1	Gallus gallus (chicken)	3	0
P31947	14-3-3 protein sigma	SFN HME1	Homo sapiens (human)	3	2
Q9QZR9	Collagen alpha-4(IV) chain	Col4a4	Mus musculus (house mouse)	3	0
P15722	Probable pectate lyase P59	LAT59	Solanum lycopersicum (tomato)	3	0
A0A8I5NDS8	Paraoxonase	PON1	Papio anubis (olive baboon)	3	0
Q9FPQ6	Vegetative cell wall protein gp1	GP1	Chlamydomonas reinhardtii	3	13
Q9JII2	Prolactin-5A1	Prl5a1 D13Wsu14e Prlpl	Mus musculus (house mouse)	3	0
A0A7K5B889	Angiotensin-converting enzyme (Fragment)	Ace	Furnarius figulus	3	0
A0A7K4Z3A9	Angiotensin-converting enzyme (Fragment)	Ace	Bucorvus abyssinicus (Abyssinian ground-hornbill)	3	0
Q05152	Voltage-dependent N-type calcium channel subunit alpha-1B	CACNA1B CACH5 CACNL1A5	Oryctolagus cuniculus (rabbit)	3	0
Q9NFL4	Hemocyanin G chain	HCG	Aphonopelma sp.	3	0
A0A068BES0	CD320 antigen isoform 002	Cd320 CD320-002	Mus musculus (house mouse)	3	0
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

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