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 **2651 - 2675** 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
A6NDG6	Glycerol-3-phosphate phosphatase	PGP	Homo sapiens (human)	1	1	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 Ewing sarcoma Hirschsprung's disease Krukenberg carcinoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma allergic asthma alternating hemiplegia of childhood asthma autonomic neuropathy autosomal dominant polycystic kidney disease basal cell carcinoma bipolar disorder bone marrow disease brain ischemia breast cancer breast carcinoma cancer carcinoma central nervous system disease central nervous system lymphoma cerebral degeneration childhood leukemia chorioamnionitis chronic myeloid leukemia colon adenocarcinoma colorectal cancer colorectal carcinoma cribriform carcinoma degenerative disc disease depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism dysthymic disorder embryoma erythromelalgia essential hypertension essential thrombocythemia familial retinoblastoma glucose intolerance granular cell carcinoma hepatocellular carcinoma hypertension inflammatory bowel disease intrinsic asthma kidney cancer large intestine cancer leukemia lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung carcinoma lymphoid leukemia lymphoma major depressive disorder melancholic depression myelodysplastic syndrome myeloid leukemia myotonic dystrophy type 1 myotonic dystrophy type 2 nervous system disease neuroblastoma neurodegenerative disease neuroectodermal tumor neuropathy neurotic disorder obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma peripheral nervous system disease polycystic kidney disease 1 polyneuropathy prediabetes syndrome retinoblastoma rhabdomyosarcoma rhinitis schizophrenia sebaceous carcinoma sexual dysfunction squamous cell carcinoma sweat gland cancer tongue squamous cell carcinoma trilateral retinoblastoma 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 varicose veins vitiligo
O75949	NALCN channel auxiliary factor 2	NALF2 FAM155B TED TMEM28	Homo sapiens (human)	4	1
O75525	KH domain-containing, RNA-binding, signal transduction-associated protein 3	KHDRBS3 SALP SLM2	Homo sapiens (human)	0	1
Q8TDW0	Volume-regulated anion channel subunit LRRC8C	LRRC8C AD158 FAD158	Homo sapiens (human)	6	5
Q9H7U1	Serine-rich coiled-coil domain-containing protein 2	CCSER2 FAM190B KIAA1128	Homo sapiens (human)	2	1
Q5NKV8	Intercellular adhesion molecule 1	ICAM1	Homo sapiens (human)	3	0
P56962	Syntaxin-17	STX17	Homo sapiens (human)	0	1
K9L7E0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9NW82	WD repeat-containing protein 70	WDR70	Homo sapiens (human)	1	1
E9PP43	Sortilin related receptor 1	SORL1	Homo sapiens (human)	2	0
P0DJD1	RANBP2-like and GRIP domain-containing protein 2	RGPD2 RANBP2L2 RGP2	Homo sapiens (human)	0	1
A0A1C8DSL6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9BWT3	Poly(A) polymerase gamma	PAPOLG PAP2 PAPG	Homo sapiens (human)	0	1
O95563	Mitochondrial pyruvate carrier 2	MPC2 BRP44	Homo sapiens (human)	0	1
G1EPZ1	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q93063	Exostosin-2	EXT2	Homo sapiens (human)	2	2	Alzheimer's disease Cenani-Lenz syndactyly syndrome Dent disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Marfan syndrome Ollier disease Pick's disease Reye syndrome achondroplasia adenosarcoma agnosia anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease cerebral degeneration cherubism chondrosarcoma cleidocranial dysplasia clubfoot congenital hypothyroidism congenital nystagmus connective tissue disease cranial nerve disease cranial nerve palsy craniosynostosis cryptorchidism developmental and epileptic encephalopathy 36 developmental coordination disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus epilepsy esophagitis essential hypertension exostosis familial hypercholesterolemia frontotemporal dementia gastroesophageal reflux disease hereditary multiple exostoses humeroradial synostosis hyperostosis hypertension hypertropia hypothyroidism immune system disease intellectual disability large intestine cancer learning disability lupus nephritis macrocytic anemia mechanical strabismus membranous glomerulonephritis metachondromatosis microcephaly mucopolysaccharidosis III mucopolysaccharidosis type IIIA myxedema nephroblastoma nonsyndromic congenital nail disorder 9 obsolete constipation ophthalmoplegia osteoarthritis osteonecrosis osteosarcoma parietal foramina pathologic nystagmus peptic esophagitis periarthritis radioulnar synostosis scoliosis situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus tendinitis tuberous sclerosis type 2 diabetes mellitus ventricular septal defect visual epilepsy
M9P9T6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P23497	Nuclear autoantigen Sp-100	SP100	Homo sapiens (human)	3	2
Q99680	G-protein coupled receptor 22	GPR22	Homo sapiens (human)	2	0
P27708	Multifunctional protein CAD	CAD	Homo sapiens (human)	5	1
Q9UJV9	Probable ATP-dependent RNA helicase DDX41	DDX41 ABS	Homo sapiens (human)	0	1
A0A186VP06	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
D3U3V4	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
I2D5I8	Apolipoprotein M (Fragment)	APOM	Homo sapiens (human)	1	0
P08949	Neuromedin-B	NMB	Homo sapiens (human)	8	1

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