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 **14951 - 14975** 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
Q13822	Ectonucleotide pyrophosphatase/phosphodiesterase family member 2	ENPP2 ATX PDNP2	Homo sapiens (human)	5	16	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 Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Pick's disease Reye syndrome actinic keratosis adult hepatocellular carcinoma alternating hemiplegia of childhood arthritis arthropathy ataxia telangiectasia autonomic neuropathy autosomal dominant cerebellar ataxia biliary atresia bladder carcinoma blood coagulation disease brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood hepatocellular carcinoma choroid plexus cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma dedifferentiated liposarcoma disease of metabolism embryoma epithelioid sarcoma fibrodysplasia ossificans progressiva fibromyalgia gallbladder disease gastroenteritis giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperthyroidism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis liposarcoma liver cancer liver cirrhosis liver disease localized scleroderma lung benign neoplasm lung cancer lung carcinoma multiple myeloma multiple sclerosis myositis ossificans nervous system disease neuroblastoma nodular prostate nonpapillary renal cell carcinoma obesity obsolete inherited blood coagulation disease ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary renal cell carcinoma pleomorphic liposarcoma prostate cancer prostate carcinoma prostatic adenoma renal carcinoma renal cell carcinoma rheumatoid arthritis sarcoma sarcomatoid renal cell carcinoma scleroderma seborrheic keratosis skin disease spindle cell sarcoma spinocerebellar ataxia type 7 systemic scleroderma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis ulcerative colitis urinary bladder cancer
P22413	Ectonucleotide pyrophosphatase/phosphodiesterase family member 1	ENPP1 M6S1 NPPS PC1 PDNP1	Homo sapiens (human)	10	45	Ehlers-Danlos syndrome HCL-V Laron syndrome McCune Albright syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired hyperkeratosis acute myocardial infarction adult astrocytic tumor allergic asthma amelogenesis imperfecta anaplastic astrocytoma anemia angioid streaks ankylosing spondylitis ankylosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autosomal dominant hypophosphatemic rickets autosomal recessive hypophosphatemic rickets autosomal recessive osteopetrosis 7 bicuspid aortic valve disease bile duct adenocarcinoma bile duct cancer bile duct carcinoma bile duct disease blindness bone disease brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease carotid artery disease cartilage disease cerebral infarction cerebrovascular disease childhood astrocytic tumor childhood cerebral astrocytoma cholangiocarcinoma chondrocalcinosis chronic kidney disease colorectal cancer colorectal carcinoma congenital hypothyroidism congenital toxoplasmosis congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis endometriosis of ovary endometriosis of uterus endometriosis enthesopathy essential hypertension exanthem fibrillary astrocytoma gemistocytic astrocytoma gestational diabetes giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance hairy cell leukemia heart disease hepatitis C hepatocellular carcinoma hereditary elliptocytosis herpes simplex high grade glioma hypercalcemia hypercementosis hyperglycemia hyperinsulinism hyperphosphatemic familial tumoral calcinosis hypertension hypophosphatemia hypothyroidism insulinoma intermittent claudication intrinsic asthma juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure large intestine cancer linear nevus sebaceous syndrome liver cancer lung benign neoplasm lung cancer lung carcinoma macrocytic anemia malignant astrocytoma melanoma mitral valve insufficiency mitral valve prolapse mongolian spot monoclonal gammopathy of uncertain significance morbid obesity mucopolysaccharidosis IV multiple epiphyseal dysplasia multiple myeloma musculoskeletal system disease myelitis myocardial infarction myopia myxedema nephritis nephrocalcinosis nephrosis neurogenic arthropathy nodular prostate nonepidermolytic palmoplantar keratoderma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 ossification of the posterior longitudinal ligament of spine osteoarthritis osteochondrodysplasia osteogenesis imperfecta osteomalacia osteopetrosis osteoporosis osteosclerosis otitis media palmoplantar keratosis pancreatic cancer pancreatic carcinoma periarthritis perinatal intestinal perforation peripheral artery disease peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma plasmacytoma pneumocystosis polycystic ovary syndrome polycythemia vera polycythemia postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pseudoxanthoma elasticum pulmonary valve stenosis pyoureter restrictive cardiomyopathy retinal disease retinitis rheumatoid arthritis rickets sarcomatoid carcinoma scoliosis sensorineural hearing loss silent myocardial infarction skin melanoma spondyloarthropathy spondylosis steatotic liver disease subependymal giant cell astrocytoma suppurative periapical periodontitis tendinitis tropical sprue tympanosclerosis 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 uremia viral infectious disease
E5RIA2	Ectonucleotide pyrophosphatase/phosphodiesterase 2	ENPP2	Homo sapiens (human)	1	0
E7EUF1	Ectonucleotide pyrophosphatase/phosphodiesterase 2	ENPP2	Homo sapiens (human)	1	0
Q5MY95	Ectonucleoside triphosphate diphosphohydrolase 8	ENTPD8	Homo sapiens (human)	4	1
Q9NQZ7	Ectonucleoside triphosphate diphosphohydrolase 7	ENTPD7 LALP1	Homo sapiens (human)	2	2
O75354	Ectonucleoside triphosphate diphosphohydrolase 6	ENTPD6 CD39L2 IL6ST2	Homo sapiens (human)	8	3
Q9Y227	Ectonucleoside triphosphate diphosphohydrolase 4	ENTPD4 KIAA0392 LALP70 LYSAL1	Homo sapiens (human)	4	3
O75355	Ectonucleoside triphosphate diphosphohydrolase 3	ENTPD3 CD39L3	Homo sapiens (human)	7	8
Q9Y5L3	Ectonucleoside triphosphate diphosphohydrolase 2	ENTPD2 CD39L1	Homo sapiens (human)	7	50
P49961	Ectonucleoside triphosphate diphosphohydrolase 1	ENTPD1 CD39	Homo sapiens (human)	6	30
Q92838	Ectodysplasin-A	EDA ED1 EDA2	Homo sapiens (human)	2	0
O14682	Ectoderm-neural cortex protein 1	ENC1 KLHL37 NRPB PIG10	Homo sapiens (human)	0	1
Q16206	Ecto-NOX disulfide-thiol exchanger 2	ENOX2 COVA1	Homo sapiens (human)	0	1
Q8TC92	Ecto-NOX disulfide-thiol exchanger 1	ENOX1	Homo sapiens (human)	1	1
Q96L15	Ecto-ADP-ribosyltransferase 5	ART5	Homo sapiens (human)	3	1	cholera
Q93070	Ecto-ADP-ribosyltransferase 4	ART4 DO DOK1	Homo sapiens (human)	5	23	carotid artery thrombosis carotid stenosis conjunctivitis
Q13508	Ecto-ADP-ribosyltransferase 3	ART3 TMART	Homo sapiens (human)	2	9	azoospermia cancer melanoma patent ductus arteriosus skin melanoma steatotic liver disease
O60447	Ecotropic viral integration site 5 protein homolog	EVI5 NB4S	Homo sapiens (human)	1	1
Q6ZMW3	Echinoderm microtubule-associated protein-like 6	EML6 EML5L	Homo sapiens (human)	2	1
Q05BV3	Echinoderm microtubule-associated protein-like 5	EML5	Homo sapiens (human)	0	1
Q9HC35	Echinoderm microtubule-associated protein-like 4	EML4 C2orf2 EMAPL4	Homo sapiens (human)	2	1
Q32P44	Echinoderm microtubule-associated protein-like 3	EML3	Homo sapiens (human)	4	1
O95834	Echinoderm microtubule-associated protein-like 2	EML2 EMAP2 EMAPL2	Homo sapiens (human)	0	1
O00423	Echinoderm microtubule-associated protein-like 1	EML1 EMAP1 EMAPL EMAPL1	Homo sapiens (human)	0	1

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