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 **15351 - 15375** 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
A0A7I2V5R8	Dipeptidyl peptidase 4	DPP4	Homo sapiens (human)	1	0
P27487	Dipeptidyl peptidase 4	DPP4 ADCP2 CD26	Homo sapiens (human)	12	84
Q9NY33	Dipeptidyl peptidase 3	DPP3	Homo sapiens (human)	2	2
Q9UHL4	Dipeptidyl peptidase 2	DPP7 DPP2 QPP	Homo sapiens (human)	7	29
A0A7I2V466	Dipeptidyl peptidase 1	CTSC	Homo sapiens (human)	1	0
H0YCY8	Dipeptidyl peptidase 1	CTSC	Homo sapiens (human)	1	0
A0A7I2V2Q8	Dipeptidyl peptidase 1	CTSC	Homo sapiens (human)	1	0
P53634	Dipeptidyl peptidase 1	CTSC CPPI	Homo sapiens (human)	5	135
A0A7I2V5C5	Dipeptidyl peptidase 1	CTSC	Homo sapiens (human)	1	0
P42658	Dipeptidyl aminopeptidase-like protein 6	DPP6	Homo sapiens (human)	8	6
Q9H4B8	Dipeptidase 3	DPEP3	Homo sapiens (human)	1	0	arteriosclerotic cardiovascular disease atherosclerosis coronary artery disease laryngeal disease tracheal disease
Q9H4A9	Dipeptidase 2	DPEP2	Homo sapiens (human)	5	6	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 Pick's disease Reye syndrome arteriosclerotic cardiovascular disease atherosclerosis cerebral degeneration coronary artery disease laryngeal disease ovarian cancer ovarian carcinoma tracheal disease
P16444	Dipeptidase 1	DPEP1 MDP RDP	Homo sapiens (human)	6	142	Camurati-Engelmann disease Crohn's colitis Crohn's disease Duchenne muscular dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SAPHO syndrome X-linked lymphoproliferative syndrome 2 adenoma amyloidosis ankylosing spondylitis arthritis arthropathy 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 bladder calculus bone cancer bone osteosarcoma breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer childhood osteosarcoma cholecystolithiasis choledocholithiasis cholelithiasis chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy dystonia embryoma epithelioid leiomyosarcoma essential hypertension facioscapulohumeral muscular dystrophy familial adenomatous polyposis 1 familial adenomatous polyposis familial hemiplegic migraine 2 familial hemiplegic migraine fibrodysplasia ossificans progressiva focal hand dystonia follicular adenoma generalized dystonia gliosarcoma heart disease hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperuricemia inflammatory bowel disease 1 inflammatory bowel disease influenza interstitial nephritis invasive ductal carcinoma large intestine cancer laryngeal disease leiomyosarcoma lepromatous leprosy limb-girdle muscular dystrophy metachondromatosis microcystic adenoma microphthalmia mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myositis ossificans myxoid leiomyosarcoma neuroendocrine carcinoma obsolete Matthew-Wood syndrome 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 osteoarthritis osteoporosis osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma periostitis peritoneal carcinoma proliferative diabetic retinopathy prostate cancer prostate carcinoma pulmonary embolism pyelitis pyelonephritis rheumatoid arthritis rippling muscle disease 2 secondary Parkinson disease secondary hypertrophic osteoarthropathy severe nonproliferative diabetic retinopathy stone in bladder diverticulum thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tracheal disease ulcerative colitis
Q9H5Q4	Dimethyladenosine transferase 2, mitochondrial	TFB2M NS5ATP5	Homo sapiens (human)	0	1
Q8WVM0	Dimethyladenosine transferase 1, mitochondrial	TFB1M	Homo sapiens (human)	0	1
O15228	Dihydroxyacetone phosphate acyltransferase	GNPAT DAPAT DHAPAT	Homo sapiens (human)	0	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 Pick's disease Reye syndrome Wilson disease X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 Zellweger syndrome attention deficit hyperactivity disorder autistic disorder autosomal dominant chondrodysplasia punctata cancer cataract cerebral degeneration chondrodysplasia punctata embryoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma intellectual disability iron metabolism disease learning disability liver cancer liver carcinoma liver cirrhosis microcephaly peroxisome biogenesis disorder 1A rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata schizophrenia scoliosis
Q12882	Dihydropyrimidine dehydrogenase [NADP(+)]	DPYD	Homo sapiens (human)	4	1
Q9BPU6	Dihydropyrimidinase-related protein 5	DPYSL5 CRMP5 ULIP6	Homo sapiens (human)	0	1
O14531	Dihydropyrimidinase-related protein 4	DPYSL4 CRMP3 ULIP4	Homo sapiens (human)	0	1
Q14195	Dihydropyrimidinase-related protein 3	DPYSL3 CRMP4 DRP3 ULIP ULIP1	Homo sapiens (human)	0	1
Q16555	Dihydropyrimidinase-related protein 2	DPYSL2 CRMP2 ULIP2	Homo sapiens (human)	11	5
Q14194	Dihydropyrimidinase-related protein 1	CRMP1 DPYSL1 ULIP3	Homo sapiens (human)	1	1
P36957	Dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial	DLST DLTS	Homo sapiens (human)	2	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 Joubert syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Wernicke-Korsakoff syndrome adrenal gland cancer amnestic disorder aniridia cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cortical dysplasia-focal epilepsy syndrome duodenum cancer glomerulonephritis heart cancer hydranencephaly hypercalcemia hypertensive retinopathy kidney disease lissencephaly nephritis nephrocalcinosis neurodegenerative disease panic disorder papillary renal cell carcinoma paraganglioma pheochromocytoma phosphorus metabolism disease pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary biliary cholangitis prostate cancer prostate carcinoma proteinuria renal carcinoma renal cell carcinoma renal osteodystrophy sarcomatoid renal cell carcinoma septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly small intestine cancer syndromic X-linked intellectual disability Najm type
P10515	Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial	DLAT DLTA	Homo sapiens (human)	0	1	Cogan syndrome Sjogren's syndrome acute myeloid leukemia adrenoleukodystrophy angioimmunoblastic T-cell lymphoma ankylosing spondylitis arteriovenous malformation autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome basal ganglia disease bile duct adenocarcinoma bile duct cancer bile duct carcinoma blepharospasm breast cancer breast carcinoma cholangiocarcinoma cholestasis congenital nystagmus congenital ptosis coronary artery disease diabetes mellitus diabetic ketoacidosis diffuse interstitial keratitis dissociated nystagmus dystonia focal hand dystonia gallbladder disease head and neck squamous cell carcinoma hepatitis A hepatitis hepatocellular carcinoma immune system disease influenza keratoconjunctivitis sicca lactic acidosis leukemia liver cancer liver cirrhosis liver disease lupus erythematosus microcephaly obsolete type 1 diabetes mellitus 9 parapsoriasis pathologic nystagmus placental insufficiency primary biliary cholangitis primary sclerosing cholangitis psoriasis psoriatic arthritis ptosis pustulosis of palm and sole pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency scleroderma sclerosing cholangitis spontaneous ocular nystagmus steatotic liver disease systemic lupus erythematosus systemic scleroderma 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 vascular disease
P09622	Dihydrolipoyl dehydrogenase, mitochondrial	DLD GCSL LAD PHE3	Homo sapiens (human)	2	2	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 Friedreich ataxia Glanzmann's thrombasthenia Grn-related frontotemporal lobar degeneration with Tdp43 inclusions 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 acute monocytic leukemia acute myocardial infarction adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma adult fibrosarcoma alexia alternating hemiplegia of childhood amyotrophic lateral sclerosis antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autonomic neuropathy bacterial sepsis benign mesothelioma brain disease brain infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiomyopathy central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia choriocarcinoma chromophobe renal cell carcinoma chronic monocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communication disorder congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc congenital disorder of glycosylation congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma cutaneous mastocytosis dementia depressive disorder diabetes mellitus diabetic ketoacidosis diffuse cutaneous mastocytosis disease of metabolism dyslexia dysthymic disorder dystonia embryoma endomyocardial fibrosis epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial hypertrophic cardiomyopathy fibrosarcoma follicular adenoma fragile X syndrome frontotemporal dementia giant cell glioblastoma glioblastoma granular cell carcinoma gray platelet syndrome hepatic coma hepatic encephalopathy hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypertensive retinopathy hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intermittent claudication islet cell tumor lactic acidosis language disorder large intestine cancer learning disability leukemia leukocyte adhesion deficiency 2 leukocyte adhesion deficiency 3 leukocyte adhesion deficiency lissencephaly liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lymphoid leukemia major depressive disorder malignant mesothelioma maple syrup urine disease mastocytosis melancholic depression methemoglobinemia microcephaly microcystic adenoma monocytic leukemia multiple myeloma multiple sclerosis myeloid leukemia myocardial infarction nervous system disease neuroblastoma neurotic disorder obsolete melancholia pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma periodontitis peripheral vascular disease placenta cancer platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 posterior myocardial infarction primary immunodeficiency disease progressive muscular atrophy prostate cancer prostate carcinoma protein C deficiency protein S deficiency pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency qualitative platelet defect renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia short chain acyl-CoA dehydrogenase deficiency silent myocardial infarction stomach cancer stomach carcinoma stuttering sulfhemoglobinemia thrombophilia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urea cycle disorder urticaria pigmentosa varicose veins vascular disease viral infectious disease visual epilepsy

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