GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

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 **17201 - 17225** 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
Q9P2P1	Protein NYNRIN	NYNRIN CGIN1 KIAA1305	Homo sapiens (human)	1	1
Q9P2P5	E3 ubiquitin-protein ligase HECW2	HECW2 KIAA1301 NEDL2	Homo sapiens (human)	0	1
Q9P2P6	StAR-related lipid transfer protein 9	STARD9 KIAA1300	Homo sapiens (human)	3	2
Q9P2R3	Rabankyrin-5	ANKFY1 ANKHZN KIAA1255	Homo sapiens (human)	1	2
Q9P2R6	Arginine-glutamic acid dipeptide repeats protein	RERE ARG ARP ATN1L KIAA0458	Homo sapiens (human)	7	2
Q9P2R7	Succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial	SUCLA2	Homo sapiens (human)	0	1	3-methylglutaconic aciduria type 4 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Down syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome achondroplasia age related macular degeneration alternating hemiplegia of childhood amnestic disorder amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy blindness central nervous system disease cerebral degeneration congenital ptosis congestive heart failure coronary artery disease cutaneous porphyria degeneration of macula and posterior pole dementia depressive disorder diabetes mellitus diabetic ketoacidosis dissociative amnesia dysthymic disorder dystonia enterocele epilepsy erythropoietic protoporphyria familial retinoblastoma focal hand dystonia frontotemporal dementia generalized dystonia herpes simplex hydrocephalus hypertropia inflammatory bowel disease 1 inflammatory bowel disease isolated elevated serum creatine phosphokinase levels lactic acidosis leukopenia lingual-facial-buccal dyskinesia macular degeneration major depressive disorder mechanical strabismus melancholic depression methylmalonic acidemia microcephaly mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy movement disease nervous system disease neuroblastoma neurodegenerative disease neuropathy neurotic disorder obesity obsolete melancholia ophthalmoplegia parasitic helminthiasis infectious disease peripheral nervous system disease ptosis retinoblastoma retrocochlear disease retrograde amnesia sensorineural hearing loss sideroblastic anemia 1 strabismus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trilateral retinoblastoma tuberculosis type 2 diabetes mellitus ulcerative colitis vascular dementia visual epilepsy
Q9P2S2	Neurexin-2	NRXN2 KIAA0921	Homo sapiens (human)	8	5
Q9P2S6	Ankyrin repeat and MYND domain-containing protein 1	ANKMY1 TSAL1 ZMYND13	Homo sapiens (human)	0	1
Q9P2T1	GMP reductase 2	GMPR2	Homo sapiens (human)	0	1
Q9P2U8	Vesicular glutamate transporter 2	SLC17A6 DNPI VGLUT2	Homo sapiens (human)	3	0
Q9P2V4	Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 1	LRIT1 LRRC21 PAL	Homo sapiens (human)	3	0
Q9P2W1	Homologous-pairing protein 2 homolog	PSMC3IP HOP2 TBPIP	Homo sapiens (human)	0	1
Q9P2W7	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1	B3GAT1 GLCATP	Homo sapiens (human)	3	3	Alport syndrome 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 Clouston syndrome Down syndrome Ewing sarcoma Felty's syndrome Goodpasture syndrome HCL-V Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Lown-Ganong-Levine syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Takayasu's arteritis Wolff-Parkinson-White syndrome Zika fever acoustic neuroma acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute lymphoblastic leukemia adult acute lymphocytic leukemia aggressive NK-cell leukemia agnosia agranulocytosis allergic asthma anaplastic astrocytoma anxiety disorder arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome axonal neuropathy bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cartilage disease cataract 5 multiple types celiac disease cellular schwannoma cerebral cavernous malformation 1 cerebral degeneration cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chromophobe renal cell carcinoma chronic NK-cell lymphocytosis chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma complex regional pain syndrome congenital myasthenic syndrome connective tissue disease coronary artery disease critical illness polyneuropathy depressive disorder diabetic ketoacidosis disease of mental health dysthymic disorder embryoma encephalomyelitis epidermolysis bullosa epithelioid sarcoma esophageal cancer esophageal carcinoma essential hypertension exostosis fibrillary astrocytoma fibrous dysplasia gastroparesis gemistocytic astrocytoma generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma glycine encephalopathy granulomatosis with polyangiitis hairy cell leukemia hemophagocytic lymphohistiocytosis hepatitis C hepatitis D high grade glioma human immunodeficiency virus infectious disease hypersensitivity vasculitis hypertension idiopathic interstitial pneumonia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma influenza intrinsic asthma juvenile pilocytic astrocytoma keratoacanthoma large intestine cancer leukemia leukopenia lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphopenia major depressive disorder malaria malignant astrocytoma malignant peripheral nerve sheath tumor melancholic depression melanoma melanotic neurilemmoma meningoencephalitis metanephric adenoma mucocutaneous leishmaniasis multiple myeloma multiple sclerosis myasthenia gravis myeloid leukemia myeloproliferative disorder with eosinophilia neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder neutropenia nonpapillary renal cell carcinoma obsolete constipation obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea osteoarthritis papillary carcinoma papillary renal cell carcinoma papilloma periapical granuloma peripheral nervous system disease phobic disorder pilocytic astrocytoma plasma cell neoplasm pleomorphic adenoma plexiform schwannoma polyarteritis nodosa polyneuropathy polyradiculoneuropathy post-traumatic stress disorder postinflammatory pulmonary fibrosis primary biliary cholangitis primary sclerosing cholangitis prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder pulmonary fibrosis renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis severe congenital neutropenia skin melanoma speech-language disorder-1 spindle cell sarcoma squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer subependymal giant cell astrocytoma sudden infant death syndrome tongue squamous cell carcinoma tuberculosis 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 ulcerative colitis uveal melanoma viral infectious disease
Q9P2X0	Dolichol-phosphate mannosyltransferase subunit 3	DPM3	Homo sapiens (human)	2	2	Duchenne muscular dystrophy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cardiomyopathy clubfoot congenital disorder of glycosylation type I congenital muscular dystrophy distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R oculopharyngeal muscular dystrophy rippling muscle disease 2
Q9P2X3	Protein IMPACT	IMPACT	Homo sapiens (human)	0	1
Q9P2Y4	Zinc finger protein 219	ZNF219	Homo sapiens (human)	4	1
Q9TNU1	HLA-Cw3 (Fragment)	HLA-Cw*03MAC	Homo sapiens (human)	1	0
Q9TP26	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9TP38	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9TPQ0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9TPQ1	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9TPR3	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9TPU0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9TPU4	MHC class I antigen HLA-B (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9TPU5	MHC class I antigen HLA-C (Fragment)	HLA-C	Homo sapiens (human)	1	0

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