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
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **13101 - 13125** of **126547** in total

« First

‹ Prev

…

521

522

523

524

525

526

527

528

529

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
P40066	mRNA export factor GLE2	GLE2 RAE1	Saccharomyces cerevisiae S288C	5	1
Q9DBY4	TLR4 interactor with leucine rich repeats	Tril Kiaa0644	Mus musculus (house mouse)	5	4
Q25263	Receptor-type adenylate cyclase B	RAC-B	Leishmania donovani	5	0
P58242	Acid sphingomyelinase-like phosphodiesterase 3b	Smpdl3b Asml3b	Mus musculus (house mouse)	5	3
Q9DCP2	Sodium-coupled neutral amino acid transporter 3	Slc38a3 Sn1 Snat3	Mus musculus (house mouse)	5	2
Q9Y487	V-type proton ATPase 116 kDa subunit a 2	ATP6V0A2	Homo sapiens (human)	5	7	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease
A0A0G2JDH9	Prominin 1	Prom1	Mus musculus (house mouse)	5	0
Q9P2D6	Protein FAM135A	FAM135A KIAA1411	Homo sapiens (human)	5	3
P08049	Neprilysin	MME	Oryctolagus cuniculus (rabbit)	5	0
Q6CW36	GPI ethanolamine phosphate transferase 1	MCD4	Kluyveromyces lactis NRRL Y-1140	5	0
Q8LPK2	ABC transporter B family member 2	ABCB2 MDR2 PGP2	Arabidopsis thaliana (thale cress)	5	0
B8NMK3	Extracellular metalloproteinase mep	mep	Aspergillus flavus NRRL3357	5	0
P16721	Protein UL11	UL11	Human herpesvirus 5 strain AD169	5	0
Q9ERS6	X-linked interleukin-1 receptor accessory protein-like 2	Il1rapl2	Mus musculus (house mouse)	5	0
Q04857	Collagen alpha-1(VI) chain	Col6a1	Mus musculus (house mouse)	5	17
Q11206	CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 4	ST3GAL4 CGS23 NANTA3 SIAT4C STZ	Homo sapiens (human)	5	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 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenoid cystic carcinoma alopecia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant intellectual developmental disorder 4 autosomal dominant intellectual developmental disorder 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 brain stem infarction campomelic dysplasia cancer carcinoma cardiomyopathy cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniometaphyseal dysplasia dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal myopathy dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis essential hypertension facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia frontotemporal dementia gallbladder disease gestational diabetes granuloma annulare hepatocellular carcinoma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypoglycemia large intestine cancer limb-girdle muscular dystrophy liver cancer liver disease major depressive disorder melancholic depression melanoma mucopolysaccharidosis IV mucopolysaccharidosis IVA muscular dystrophy myelitis myocardial infarction neuropathy neurotic disorder nonpapillary renal cell carcinoma 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 obsolete melancholia obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoporosis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis retrograde amnesia salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease thrombophilia tongue squamous cell carcinoma 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
Q41438	3-hydroxy-3-methylglutaryl-coenzyme A reductase 3	HMG3	Solanum tuberosum (potato)	5	0
Q9FH06	Serine carboxypeptidase-like 41	SCPL41	Arabidopsis thaliana (thale cress)	5	0
Q92615	La-related protein 4B	LARP4B KIAA0217 LARP5	Homo sapiens (human)	5	1
Q7RYY1	Putative lipase atg15	atg15	Neurospora crassa OR74A	5	0
Q14833	Metabotropic glutamate receptor 4	GRM4 GPRC1D MGLUR4	Homo sapiens (human)	5	0
Q1PHM6	Envelope glycoprotein gp160	env	Human immunodeficiency virus 1	5	0
A8MTB9	Carcinoembryonic antigen-related cell adhesion molecule 18	CEACAM18	Homo sapiens (human)	5	1
Q12889	Oviduct-specific glycoprotein	OVGP1 MUC9 OGP	Homo sapiens (human)	5	1	bagassosis cancer centronuclear myopathy ciliary body disease colorectal cancer colorectal carcinoma congenital structural myopathy embryoma endometrial carcinoma endosalpingiosis iris disease large intestine cancer laryngitis ovarian cancer ovarian carcinoma panuveitis transient myeloproliferative syndrome tubular aggregate myopathy 1 uveitis
Q06BH3	Protein STRUBBELIG-RECEPTOR FAMILY 1	SRF1	Arabidopsis thaliana (thale cress)	5	0

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements