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 **1176 - 1200** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9Y4K1	Beta/gamma crystallin domain-containing protein 1	CRYBG1 AIM1	Homo sapiens (human)	8	6	allergic asthma asthma cancer intrinsic asthma melanoma multiple myeloma patent ductus arteriosus prostate cancer prostate carcinoma skin melanoma
P26022	Pentraxin-related protein PTX3	PTX3 TNFAIP5 TSG14	Homo sapiens (human)	3	6
Q5IJ48	Protein crumbs homolog 2	CRB2	Homo sapiens (human)	15	6
Q03164	Histone-lysine N-methyltransferase 2A	KMT2A ALL1 CXXC7 HRX HTRX MLL MLL1 TRX1	Homo sapiens (human)	26	6
Q96DA0	Pancreatic adenocarcinoma up-regulated factor	ZG16B PAUF	Homo sapiens (human)	2	6
Q9NRZ9	Lymphoid-specific helicase	HELLS PASG SMARCA6	Homo sapiens (human)	3	6
Q8NBS9	Thioredoxin domain-containing protein 5	TXNDC5 TLP46	Homo sapiens (human)	14	6
Q9UJT0	Tubulin epsilon chain	TUBE1 TUBE	Homo sapiens (human)	1	6
Q14157	Ubiquitin-associated protein 2-like	UBAP2L KIAA0144 NICE4	Homo sapiens (human)	105	6
O95857	Tetraspanin-13	TSPAN13 NET6 TM4SF13	Homo sapiens (human)	4	6
P49792	E3 SUMO-protein ligase RanBP2	RANBP2 NUP358	Homo sapiens (human)	68	6
P13866	Sodium/glucose cotransporter 1	SLC5A1 NAGT SGLT1	Homo sapiens (human)	4	6	Bartter disease Conn's syndrome Fanconi syndrome Waterhouse-Friderichsen syndrome X-linked juvenile retinoschisis 1 abdominal obesity-metabolic syndrome 1 acute myocardial infarction adenocarcinoma adenoma arteriosclerotic cardiovascular disease atherosclerosis bacterial infectious disease bacterial sepsis brain stem infarction breast cancer breast carcinoma calcinosis calcium metabolism disease cancer cardiomyopathy cardiovascular system disease cerebral artery occlusion cerebral infarction cerebrovascular disease cholera colon adenocarcinoma congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cutaneous leishmaniasis cystinosis diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis essential hypertension familial hypertrophic cardiomyopathy galactosemia glomerulonephritis glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma hypercalcemia hyperglycemia hypertension hypertrophic cardiomyopathy hypoglycemia intestinal atresia kidney disease kidney failure kwashiorkor lactic acidosis listeriosis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma marasmus middle cerebral artery infarction myocardial infarction nephritis nephrocalcinosis nephrosis nutmeg liver nutrition disease obesity obsolete type 1 diabetes mellitus 9 optic atrophy 1 optic atrophy pancreatic cancer pancreatic carcinoma phosphorus metabolism disease pneumonia prediabetes syndrome primary hyperaldosteronism protein-energy malnutrition pyoureter renal glycosuria silent myocardial infarction squamous cell carcinoma tongue squamous cell carcinoma toxic shock syndrome tropical sprue tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus
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
P01127	Platelet-derived growth factor subunit B	PDGFB PDGF2 SIS	Homo sapiens (human)	3	6
Q86SJ2	Amphoterin-induced protein 2	AMIGO2 ALI1	Homo sapiens (human)	9	6
P43356	Melanoma-associated antigen 2	MAGEA2 MAGEA2B MAGE2 MAGEA2 MAGEA2A	Homo sapiens (human)	1	6
Q9H2A7	C-X-C motif chemokine 16	CXCL16 SCYB16 SRPSOX	Homo sapiens (human)	14	6
O60242	Adhesion G protein-coupled receptor B3	ADGRB3 BAI3 KIAA0550	Homo sapiens (human)	14	6
P10809	60 kDa heat shock protein, mitochondrial	HSPD1 HSP60	Homo sapiens (human)	5	6
Q68CJ9	Cyclic AMP-responsive element-binding protein 3-like protein 3	CREB3L3 CREBH	Homo sapiens (human)	6	6
Q7Z589	BRCA2-interacting transcriptional repressor EMSY	EMSY C11orf30	Homo sapiens (human)	73	6
Q96PE1	Adhesion G protein-coupled receptor A2	ADGRA2 GPR124 KIAA1531 TEM5	Homo sapiens (human)	12	6
P02458	Collagen alpha-1(II) chain	COL2A1	Homo sapiens (human)	12	6
Q8TBP5	Membrane protein FAM174A	FAM174A NS5ATP6 TMEM157	Homo sapiens (human)	3	6
P31943	Heterogeneous nuclear ribonucleoprotein H	HNRNPH1 HNRPH HNRPH1	Homo sapiens (human)	7	6

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