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 **17476 - 17500** 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
Q9UN70	Protocadherin gamma-C3	PCDHGC3 PCDH2	Homo sapiens (human)	10	7
P0DTE8	Alpha-amylase 1C	AMY1C AMY1	Homo sapiens (human)	2	7
P61812	Transforming growth factor beta-2 proprotein	TGFB2	Homo sapiens (human)	4	7
Q5CZC0	Fibrous sheath-interacting protein 2	FSIP2	Homo sapiens (human)	13	7
Q9Y240	C-type lectin domain family 11 member A	CLEC11A CLECSF3 LSLCL SCGF	Homo sapiens (human)	6	7
Q76M96	Coiled-coil domain-containing protein 80	CCDC80 DRO1 URB	Homo sapiens (human)	21	7
Q86VZ4	Low-density lipoprotein receptor-related protein 11	LRP11	Homo sapiens (human)	16	7
O95897	Noelin-2	OLFM2 NOE2	Homo sapiens (human)	6	7
Q96NY8	Nectin-4	NECTIN4 LNIR PRR4 PVRL4	Homo sapiens (human)	2	7
P01222	Thyrotropin subunit beta	TSHB	Homo sapiens (human)	1	7
Q9H2E6	Semaphorin-6A	SEMA6A KIAA1368 SEMAQ	Homo sapiens (human)	8	8
P35499	Sodium channel protein type 4 subunit alpha	SCN4A	Homo sapiens (human)	13	8
P12645	Bone morphogenetic protein 3	BMP3 BMP3A	Homo sapiens (human)	12	8
Q8NAT1	Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2	POMGNT2 AGO61 C3orf39 EOGTL GTDC2	Homo sapiens (human)	6	8	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome acute myeloid leukemia 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 cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A8 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly malaria microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 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 obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
P01909	HLA class II histocompatibility antigen, DQ alpha 1 chain	HLA-DQA1	Homo sapiens (human)	5	8
Q9HAR2	Adhesion G protein-coupled receptor L3	ADGRL3 KIAA0768 LEC3 LPHN3	Homo sapiens (human)	14	8
O00461	Golgi integral membrane protein 4	GOLIM4 GIMPC GOLPH4 GPP130	Homo sapiens (human)	27	8
P12544	Granzyme A	GZMA CTLA3 HFSP	Homo sapiens (human)	1	8
Q6WRI0	Immunoglobulin superfamily member 10	IGSF10 CMF608	Homo sapiens (human)	21	8
P16109	P-selectin	SELP GMRP GRMP	Homo sapiens (human)	13	8	Burkitt lymphoma Evans' syndrome Gilbert syndrome Glanzmann's thrombasthenia Goodpasture syndrome Kawasaki disease Proteus syndrome St. Louis encephalitis Takayasu's arteritis Zika fever abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute chest syndrome acute myocardial infarction age related macular degeneration agranulocytosis allergic asthma ankylosing spondylitis antiphospholipid syndrome antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura bacterial sepsis beta thalassemia bilirubin metabolic disorder blood coagulation disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease carotid artery disease cerebral artery occlusion cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon carcinoma colorectal cancer common cold congenital heart disease congestive heart failure corneal dystrophy coronary artery disease coronary thrombosis cystic fibrosis degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dysthymic disorder embryoma encephalitis encephalomyelitis epithelioid sarcoma essential hypertension essential thrombocythemia familial combined hyperlipidemia familial hyperlipidemia focal segmental glomerulosclerosis gallbladder disease gastroenteritis gastrointestinal stromal tumor giant cell glioblastoma glioblastoma glomerulonephritis granulomatosis with polyangiitis gray platelet syndrome head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypertension hypoglycemia ileitis ileocolitis immune system disease intermediate coronary syndrome intrinsic asthma keratosis follicularis kidney disease kidney failure kwashiorkor leukopenia liver cancer liver carcinoma liver disease lung adenocarcinoma lung cancer lung carcinoma lupus erythematosus macular degeneration major depressive disorder marasmus melancholic depression mongolian spot multiple myeloma multiple sclerosis myelitis myelofibrosis myocardial infarction myotonic dystrophy type 1 myotonic dystrophy type 2 nasopharyngitis nasopharynx carcinoma nephritis neuroblastoma neurotic disorder neutropenia nonpapillary renal cell carcinoma nutmeg liver nutrition disease obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma parapsoriasis peripheral artery disease platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 pneumonia polyarteritis nodosa portal vein thrombosis primary pulmonary hypertension proliferative diabetic retinopathy protein C deficiency protein S deficiency protein-energy malnutrition pseudoxanthoma elasticum psoriasis pulmonary embolism pustulosis of palm and sole qualitative platelet defect renal carcinoma renal cell carcinoma rheumatoid arthritis sarcoma sarcomatoid renal cell carcinoma severe congenital neutropenia sick sinus syndrome sickle cell anemia silent myocardial infarction spindle cell sarcoma systemic lupus erythematosus thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia transient cerebral ischemia 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 vertebrobasilar insufficiency von Willebrand's disease 3 von Willebrand's disease
Q6ZNA5	Ferric-chelate reductase 1	FRRS1 SDFR2 SDR2	Homo sapiens (human)	6	8
O95427	GPI ethanolamine phosphate transferase 1	PIGN MCD4	Homo sapiens (human)	4	8	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia 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 autosomal dominant polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
Q14390	Glutathione hydrolase light chain 2	GGTLC2 GGTL4	Homo sapiens (human)	2	8
Q96HD1	Protein disulfide isomerase CRELD1	CRELD1 CIRRIN	Homo sapiens (human)	5	8
Q9NZU0	Leucine-rich repeat transmembrane protein FLRT3	FLRT3 KIAA1469	Homo sapiens (human)	9	8

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