GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
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
Q86VE9	Serine incorporator 5	SERINC5 C5orf12	3	0
Q5QGZ9	C-type lectin domain family 12 member A	CLEC12A CLL1 DCAL2 MICL	3	0	Crohn's colitis Crohn's disease Richter's syndrome acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia arthritis arthropathy cancer childhood leukemia chronic fatigue syndrome chronic lymphocytic leukemia chronic myeloid leukemia dermatophytosis embryoma encephalitis encephalomyelitis essential thrombocythemia fungal infectious disease immune system disease inflammatory bowel disease 1 inflammatory bowel disease leukemia lymphoblastic lymphoma lymphocytic choriomeningitis lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma rheumatoid arthritis ulcerative colitis
Q15428	Splicing factor 3A subunit 2	SF3A2 SAP62	3	1
F8VV56	CD63 molecule	CD63	3	0
P31358	CAMPATH-1 antigen	CD52 CDW52 HE5	3	0
P68032	Actin, alpha cardiac muscle 1	ACTC1 ACTC	3	2
O60503	Adenylate cyclase type 9	ADCY9 KIAA0520	3	3
P78380	Oxidized low-density lipoprotein receptor 1	OLR1 CLEC8A LOX1	3	0	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Cockayne syndrome Kawasaki disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis acute chest syndrome acute myocardial infarction adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation bone osteosarcoma brain stem infarction breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease carpal tunnel syndrome central sleep apnea cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma choriocarcinoma chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endomyocardial fibrosis essential hypertension familial hypercholesterolemia familial hyperlipidemia gallbladder disease generalized atherosclerosis gestational diabetes giant cell glioblastoma glioblastoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma hyperhomocysteinemia hypertension hypertrophic cardiomyopathy juvenile rheumatoid arthritis keratitis keratoconjunctivitis kidney failure large intestine cancer liver cancer liver disease lung adenocarcinoma lung cancer multiple sclerosis multiple system atrophy myocardial infarction nutmeg liver obesity osteoarthritis osteosarcoma pancreatic cancer pancreatic carcinoma parapsoriasis placenta cancer postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole renal osteodystrophy rheumatoid arthritis seborrheic keratosis sickle cell anemia silent myocardial infarction skin disease transient cerebral ischemia tubular adenocarcinoma type 2 diabetes mellitus vascular disease vertebrobasilar insufficiency
P15382	Potassium voltage-gated channel subfamily E member 1	KCNE1	3	0
Q05996	Zona pellucida sperm-binding protein 2	ZP2 ZPA	3	0
Q9P2D0	Inhibitor of Bruton tyrosine kinase	IBTK BTKI KIAA1417	3	3
Q969Y0	NXPE family member 3	NXPE3 FAM55C	3	0
A6NHS7	MANSC domain-containing protein 4	MANSC4	3	0
Q95IC0	MHC class I chain-related protein A (Fragment)	MICA	3	0
O94761	ATP-dependent DNA helicase Q4	RECQL4 RECQ4	3	1
P46695	Radiation-inducible immediate-early gene IEX-1	IER3 DIF2 IEX1 PRG1	3	1
Q8WTT0	C-type lectin domain family 4 member C	CLEC4C BDCA2 CLECSF11 CLECSF7 DLEC HECL	3	0
P01127	Platelet-derived growth factor subunit B	PDGFB PDGF2 SIS	3	6
Q8IYG2	Glypican-3	GPC3	3	0
A0A7D9C115	MHC Class I chain-related protein	MICA	3	0
H3BS21	Haptoglobin (Fragment)	HP	3	0

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