GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **1276 - 1300** of **1582** in total

« First

‹ Prev

…

48

49

50

51

52

53

54

55

56

…

Next ›

Last »
Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
50	aconitase 2	ACO2 Aliases: ACONM aconitate hydratase, mitochondrial mitochondrial aconitase	Homo sapiens (human)	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 Crohn's colitis Crohn's disease Foster-Kennedy syndrome Friedreich ataxia 1 Friedreich ataxia Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome X-linked nonsyndromic deafness achromatopsia acquired color blindness adult respiratory distress syndrome autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness bipolar disorder blue color blindness breast cancer breast carcinoma cancer central nervous system disease cerebral degeneration clear cell renal cell carcinoma color blindness colorectal cancer colorectal carcinoma congenital nystagmus cystic fibrosis demyelinating polyneuropathy dissociated nystagmus dominant optic atrophy plus syndrome embryoma epilepsy fumarase deficiency fundus dystrophy hepatocellular carcinoma hypertropia idiopathic interstitial pneumonia infantile cerebellar-retinal degeneration inflammatory bowel disease 1 inflammatory bowel disease insulinoma kidney cancer large intestine cancer lingual-facial-buccal dyskinesia liver cancer mechanical strabismus mitochondrial DNA depletion syndrome movement disease multiple sclerosis neurodegenerative disease newborn respiratory distress syndrome nutritional optic neuropathy obsolete autosomal recessive nonsyndromic deafness 105 ophthalmoplegia optic atrophy 1 optic atrophy 9 optic atrophy optic nerve disease pathologic nystagmus postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pulmonary fibrosis red color blindness red-green color blindness renal carcinoma renal cell carcinoma schizophrenia spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ulcerative colitis visual epilepsy visual pathway disease
48	aconitase 1	ACO1 Aliases: IREBP IRP1 aconitate hydratase, cytoplasmic cytosplasmic aconitase soluble aconitase	Homo sapiens (human)	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 Down syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wilson disease acquired polycythemia adrenal gland cancer age related macular degeneration anemia arthritis arthropathy bipolar disorder cancer cerebral degeneration deficiency anemia degeneration of macula and posterior pole duodenal ulcer duodenum cancer dysplastic nevus syndrome embryoma erythropoietin polycythemia essential hypertension familial erythrocytosis 2 heart cancer hemochromatosis type 1 hemochromatosis hepatocellular carcinoma hypertension hypochromic anemia iron metabolism disease leech infestation liver cancer macrocytic anemia macular degeneration melanoma metabolic dysfunction-associated steatotic liver disease microcytic anemia myiasis neuroblastoma osteoarthritis pancreatic cancer pancreatic carcinoma parapsoriasis pheochromocytoma polycythemia vera polycythemia porphyria prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole skin melanoma small intestine cancer stress polycythemia toxoplasmosis
43	acetylcholinesterase (Yt blood group)	ACHE Aliases: Yt blood group	Homo sapiens (human)	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 B-cell lymphoma Balo concentric sclerosis Chagas disease Clostridium difficile colitis Creutzfeldt-Jakob disease Duchenne muscular dystrophy Gamstorp-Wohlfart syndrome Gerstmann-Straussler-Scheinker syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IGSF1 deficiency syndrome Japanese encephalitis Kawasaki disease Lafora disease Lambert-Eaton myasthenic syndrome Lewy body dementia Marfan syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Noonan syndrome 1 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peutz-Jeghers syndrome Pick's disease Q fever Reye syndrome Schwartz-Jampel syndrome 1 Wilson-Turner syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute stress disorder adrenoleukodystrophy adult medulloblastoma allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anterior horn cell disease anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy 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 distal hereditary motor neuronopathy 1 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 bacterial meningitis bacterial sepsis bipolar disorder bladder carcinoma blood platelet disease brain cancer brain disease breast cancer breast carcinoma cancer cardiac arrest cardiovascular system disease carotid artery disease cauda equina neoplasm central nervous system disease central nervous system origin vertigo centronuclear myopathy X-linked centronuclear myopathy cerebellar ataxia cerebellar disease cerebral atherosclerosis cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease chancroid childhood cerebral astrocytoma childhood disintegrative disease childhood leukemia childhood medulloblastoma chromophobe renal cell carcinoma chronic kidney disease chronic monocytic leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cognitive disorder collecting duct carcinoma colon cancer colonic benign neoplasm colonic pseudo-obstruction colorectal cancer colorectal carcinoma congenital hypothyroidism congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myasthenic syndrome 5 congenital myasthenic syndrome congenital myopathy 1A congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital structural myopathy congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome conversion disorder coronary artery disease coronary thrombosis cystic fibrosis dementia dengue disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism dissociative amnesia dissociative disorder distal myopathy dysthymic disorder dystonia embryoma endocrine exophthalmos endometritis enophthalmos epilepsy episodic ataxia type 1 essential thrombocythemia facioscapulohumeral muscular dystrophy familial hyperlipidemia fibrillary astrocytoma fibromyalgia focal epilepsy frontotemporal dementia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder glaucoma head and neck squamous cell carcinoma heart disease hemiplegia hepatocellular carcinoma high grade glioma hyperglycemia hypothyroidism idiopathic scoliosis immune system disease impotence inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intracranial arteriosclerosis intrinsic asthma irritable bowel syndrome juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma kidney cancer large intestine cancer laryngeal squamous cell carcinoma lateral sclerosis learning disability leptospirosis leukemia limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma liver cirrhosis liver disease lower respiratory tract disease lung benign neoplasm lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphogranuloma venereum major depressive disorder malaria malignant astrocytoma medulloblastoma medullomyoblastoma megaconial type congenital muscular dystrophy melancholic depression melanoma melanotic medulloblastoma migraine morbid obesity motor neuron disease movement disease multiple epiphyseal dysplasia multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myasthenia gravis myelodysplastic syndrome myelomeningocele myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis myotonic dystrophy type 2 myxedema narcolepsy nasal cavity disease necrotizing ulcerative gingivitis nemaline myopathy nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neurofibroma neuromuscular disease neuromuscular junction disease neurotic disorder nonpapillary renal cell carcinoma normocytic anemia nutmeg liver obesity 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 constipation obsolete exophthalmos obsolete melancholia obsolete ymphosarcoma oculopharyngeal muscular dystrophy orbital disease osteochondrodysplasia osteoporosis ovarian cancer overnutrition papillary adenocarcinoma papillary renal cell carcinoma paranasal sinus disease partial motor epilepsy perineurioma peripheral nerve sheath neoplasm peripheral nervous system neoplasm persian gulf syndrome phobic disorder pilocytic astrocytoma polydactyly premature ejaculation primary pulmonary hypertension prion disease progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma psychologic dyspareunia psychotic disorder renal carcinoma renal cell carcinoma retrograde amnesia rigid spine muscular dystrophy 1 rippling muscle disease 2 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma sleeping sickness spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal muscular atrophy sporadic breast cancer status epilepticus stomach cancer stomach carcinoma subacute delirium subependymal giant cell astrocytoma substance abuse substance-related disorder temporal arteritis teratocarcinoma tethered spinal cord syndrome thanatophoric dysplasia thrombocytopenia thyroid gland papillary carcinoma trypanosomiasis tuberous sclerosis type 1 diabetes mellitus type 2 diabetes mellitus typhus ulcerative colitis upper respiratory tract disease urinary bladder cancer varicose veins vascular dementia viral infectious disease visual epilepsy vitiligo von Hippel-Lindau disease yaws yellow fever
32	acetyl-CoA carboxylase beta	ACACB Aliases: ACACbeta ACC-beta ACC2 ACCB ACCbeta HACC275 acetyl-CoA carboxylase 2	Homo sapiens (human)	B-cell lymphoma Clostridium difficile colitis Clouston syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myocardial infarction adenoid cystic carcinoma arteriosclerotic cardiovascular disease atherosclerosis cancer carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis head and neck squamous cell carcinoma high grade glioma hypopharynx cancer kidney disease large intestine cancer major depressive disorder metabolic dysfunction-associated steatotic liver disease morbid obesity muscular disease myocardial infarction nephritis nephrosis neurotic disorder nutmeg liver obesity obsolete ymphosarcoma pancreatic ductal adenocarcinoma perinatal necrotizing enterocolitis pyoureter salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma silent myocardial infarction steatotic liver disease type 2 diabetes mellitus viral infectious disease
31	acetyl-CoA carboxylase alpha	ACACA Aliases: ACACalpha ACC-alpha ACC1 ACCA ACCalpha Acac1 acetyl-CoA carboxylase 1 hACC1	Homo sapiens (human)	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 B-cell lymphoma Bloch-Sulzberger syndrome Clouston syndrome Crohn's colitis Crohn's disease Graves' disease IgA glomerulonephritis Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wernicke-Korsakoff syndrome Wilson disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoid cystic carcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adult respiratory distress syndrome agenesis of the corpus callosum with peripheral neuropathy allergic rhinitis amyotrophic lateral sclerosis type 1 ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anorexia nervosa anxiety disorder aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ataxia telangiectasia atherosclerosis atrophic gastritis attention deficit hyperactivity disorder atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune hepatitis benign mesothelioma bipolar disorder brain stem infarction breast adenoid cystic carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma cardiomyopathy cardiovascular system disease celiac disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism duodenum cancer dysthymic disorder embryoma endometriosis of uterus endometriosis endomyocardial fibrosis epidermal appendage tumor esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial periodic paralysis focal segmental glomerulosclerosis follicular adenoma gallbladder disease generalized anxiety disorder gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis head and neck squamous cell carcinoma heart cancer heart disease heart valve disease hemochromatosis hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertension hyperthyroidism hypertrichosis hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypomelanosis of Ito inflammatory bowel disease 1 inflammatory bowel disease iron metabolism disease juvenile rheumatoid arthritis kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leprosy leukemia liver cancer liver carcinoma liver disease luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder malaria malignant mesothelioma malignant pleural mesothelioma megaconial type congenital muscular dystrophy melancholic depression metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease microcystic adenoma middle cerebral artery infarction migraine mitochondrial metabolism disease mitochondrial myopathy mitral valve disease muscular disease muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myocardial infarction myopathy nemaline myopathy nephritis nephrosis neuropathy neurotic disorder newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsessive-compulsive disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma ovarian cancer ovarian carcinoma papillary adenoma papillary renal cell carcinoma paraganglioma parapsoriasis periodontitis peripheral nervous system disease peroxisome biogenesis disorder 7A pheochromocytoma phobic disorder placental insufficiency polycystic ovary syndrome polyneuropathy primary ovarian insufficiency prostate adenocarcinoma prostate cancer prostate carcinoma psoriasis psoriatic arthritis pulmonary tuberculosis pustulosis of palm and sole pyoureter renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis rigid spine muscular dystrophy 1 salivary gland adenoid cystic carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma seminoma silent myocardial infarction skin benign neoplasm skin cancer small intestine cancer steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder systemic lupus erythematosus systemic scleroderma testicular cancer testis seminoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyrotoxicosis trichuriasis tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis viral infectious disease visual epilepsy
10449	acetyl-CoA acyltransferase 2	ACAA2 Aliases: DSAEC mitochondrial 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	adult respiratory distress syndrome arthritis arthropathy beta-ketothiolase deficiency hepatocellular carcinoma liver cancer newborn respiratory distress syndrome osteoarthritis
30	acetyl-CoA acyltransferase 1	ACAA1 Aliases: Lnc-Myd88 peroxisomal 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	B-cell lymphoma Langerhans-cell histiocytosis Zellweger syndrome allergic asthma asthma beta-ketothiolase deficiency carotid artery disease hepatocellular carcinoma intrinsic asthma liver cancer lymphoma non-Hodgkin lymphoma obsolete ymphosarcoma reticulosarcoma
39	acetyl-CoA acetyltransferase 2	ACAT2 Aliases: Acetyl-CoA acetyltransferase, cytosolic acetoacetyl Coenzyme A thiolase	Homo sapiens (human)	amyotrophic lateral sclerosis androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis beta-ketothiolase deficiency breast cancer cholecystolithiasis choledocholithiasis cholelithiasis choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease hepatitis C hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease liver cancer nutmeg liver papillary renal cell carcinoma premature menopause progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma syndromic X-linked intellectual disability type 10 ulcerative colitis
38	acetyl-CoA acetyltransferase 1	ACAT1 Aliases: THIL acetoacetyl Coenzyme A thiolase	Homo sapiens (human)	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 Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Crohn's colitis Crohn's disease Pick's disease Reye syndrome adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland hyperfunction adrenocortical carcinoma adult hepatocellular carcinoma age related macular degeneration agnosia alopecia amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ataxia telangiectasia atherosclerosis bacterial sepsis beta-ketothiolase deficiency bronchus cancer bronchus carcinoma cancer carbohydrate metabolic disorder cardiovascular system disease central nervous system cancer cerebral degeneration chancroid childhood hepatocellular carcinoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cribriform carcinoma cystathioninuria degeneration of macula and posterior pole developmental coordination disorder diabetes mellitus diarrhea disease of metabolism dry eye syndrome embryoma end stage renal disease epilepsy essential hypertension familial hyperlipidemia familial nephrotic syndrome focal epilepsy gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma heart disease hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hypertension hyperuricemia hypoglycemia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder intellectual disability kwashiorkor lactic acidosis large intestine cancer learning disability leptospirosis lipoid nephrosis liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lymphogranuloma venereum macular degeneration malignant teratoma marasmus mature teratoma mixed glioma necrotizing ulcerative gingivitis nephrotic syndrome neuroblastoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete Cushing's syndrome papillary renal cell carcinoma partial motor epilepsy pneumocystosis primary hyperaldosteronism prostate cancer prostate carcinoma protein-energy malnutrition rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma steatotic liver disease syndromic X-linked intellectual disability 94 teratoma thrombocytosis trypanosomiasis tubular adenocarcinoma type 2 diabetes mellitus tyrosinemia type I tyrosinemia ulcerative colitis urea cycle disorder uterine cancer uterine corpus cancer visual epilepsy xanthomatosis xerophthalmia yaws
65985	acetoacetyl-CoA synthetase	AACS Aliases: ACSF1 FLJ12389 SUR-5 acyl-CoA synthetase family member 1	Homo sapiens (human)	acute myeloid leukemia bacterial sepsis idiopathic scoliosis neuroblastoma obesity steatotic liver disease
55347	abhydrolase domain containing 10, depalmitoylase	ABHD10 Aliases: FLJ11342 Mycophenolic acid acyl-glucuronide esterase, mitochondrial	Homo sapiens (human)
150223	YdjC chitooligosaccharide deacetylase homolog	YDJC	Homo sapiens (human)	bronchus cancer bronchus carcinoma celiac disease hepatitis B inflammatory bowel disease 1 inflammatory bowel disease lung cancer lung carcinoma parapsoriasis psoriasis pustulosis of palm and sole ulcerative colitis
7512	X-prolyl aminopeptidase 2	XPNPEP2	Homo sapiens (human)	acquired angioedema androgen insensitivity syndrome angioedema cancer cervical adenocarcinoma cervical cancer cervix carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hereditary angioedema nonpapillary renal cell carcinoma papillary renal cell carcinoma premature menopause primary cutaneous amyloidosis primary ovarian insufficiency prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
11091	WD repeat domain 5	WDR5	Homo sapiens (human)	congenital heart disease
23038	WD and tetratricopeptide repeats 1	WDTC1	Homo sapiens (human)	obesity
79679	V-set domain containing T cell activation inhibitor 1	VTCN1 Aliases: B7 family member, H4 B7 superfamily member 1 B7-H4 B7H4 B7S1 B7x FLJ22418	Homo sapiens (human)	B-cell lymphoma IgA glomerulonephritis Langerhans-cell histiocytosis Sjogren's syndrome adenocarcinoma adenoma adult lymphoma arthritis arthropathy atrophic gastritis autoimmune disease autoimmune lymphoproliferative syndrome benign breast phyllodes tumor bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma breast ductal carcinoma breast malignant phyllodes tumor bronchus cancer bronchus carcinoma cancer carcinoma celiac disease central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood leukemia childhood lymphoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma ciliary body disease clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma common wart complement deficiency cribriform carcinoma cutaneous Paget's disease depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy embryoma endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma gastric adenocarcinoma gastritis gastroenteritis giant cell glioblastoma glioblastoma glomerulonephritis granular cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma ileitis ileocolitis immune system disease intrahepatic cholangiocarcinoma invasive ductal carcinoma iris disease juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease large intestine cancer laryngeal carcinoma larynx cancer leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphoma melanoma membranous glomerulonephritis microphthalmia myeloproliferative disorder with eosinophilia nephritis nephrosis neurogenic arthropathy non-Hodgkin lymphoma nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma panuveitis papillary carcinoma papillary renal cell carcinoma placental insufficiency pleural tuberculosis primary biliary cholangitis primary immunodeficiency disease pyoureter renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma synovial sarcoma systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma 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 urinary bladder cancer uterine corpus cancer uveitis uveoparotid fever
80328	UL16 binding protein 2	ULBP2 Aliases: RAET1H	Homo sapiens (human)	acute myeloid leukemia bone osteosarcoma cancer childhood leukemia childhood osteosarcoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma familial retinoblastoma large intestine cancer multiple myeloma osteosarcoma pancreatic cancer pancreatic carcinoma retinoblastoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma trilateral retinoblastoma
80329	UL16 binding protein 1	ULBP1 Aliases: RAET1I	Homo sapiens (human)	Crohn's colitis Crohn's disease Kawasaki disease adult lymphoma bone osteosarcoma bronchus cancer bronchus carcinoma cancer embryoma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis C hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma osteosarcoma stomach cancer stomach carcinoma ulcerative colitis
80146	UDP-glucuronate decarboxylase 1	UXS1 Aliases: FLJ23591 SDR6E1 UGD short chain dehydrogenase/reductase family 6E, member 12	Homo sapiens (human)	bipolar disorder hereditary multiple exostoses schizoaffective disorder schizophrenia schizophreniform disorder
7360	UDP-glucose pyrophosphorylase 2	UGP2 Aliases: SVUGP2 UGPP1 UTP--glucose-1-phosphate uridylyltransferase	Homo sapiens (human)	cancer central nervous system cancer classic galactosemia cystinuria developmental and epileptic encephalopathy 83 galactokinase deficiency galactosemia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma paroxysmal nonkinesigenic dyskinesia 1
55757	UDP-glucose glycoprotein glucosyltransferase 2	UGGT2 Aliases: FLJ10873 FLJ11485 HUGT2 MGC117360 MGC150689 MGC87276 UDP-glucose:glycoprotein glucosyltransferase 2	Homo sapiens (human)	acute myocardial infarction cancer coronary thrombosis diabetes mellitus embryoma myocardial infarction silent myocardial infarction type 2 diabetes mellitus
56886	UDP-glucose glycoprotein glucosyltransferase 1	UGGT1 Aliases: HUGT1	Homo sapiens (human)	Crigler-Najjar syndrome Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha 1-antitrypsin deficiency beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis embryoma epilepsy gallbladder disease hepatitis C hepatitis D leukopenia liver disease neonatal jaundice neutropenia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia visual epilepsy xeroderma pigmentosum group D
7357	UDP-glucose ceramide glucosyltransferase	UGCG Aliases: GCS ceramide glucosyltransferase glucosylceramide synthase	Homo sapiens (human)	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 Fabry disease Gaucher's disease type I Gaucher's disease Niemann-Pick disease type C1 Niemann-Pick disease Pick's disease Reye syndrome Sandhoff disease acute myeloid leukemia aggressive NK-cell leukemia amyotrophic lateral sclerosis anemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cerebral artery occlusion cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus corneal disease coronary artery disease cystic kidney disease dementia depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma double outlet right ventricle dysthymic disorder embryoma epilepsy essential hypertension giant cell glioblastoma glioblastoma glycine encephalopathy head and neck cancer head and neck squamous cell carcinoma hematologic cancer hemolytic anemia hepatocellular carcinoma high grade glioma hydrocephalus hyperglycemia hypertension intellectual disability invasive ductal carcinoma keratoconus kidney disease learning disability leukemia lipid storage disease liver cancer lung cancer lung non-small cell carcinoma macrocytic anemia major depressive disorder medulloblastoma medulloepithelioma melancholic depression multiple myeloma myelomeningocele narcolepsy neuroectodermal tumor neurotic disorder non-congenital cyst of kidney obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete melancholia obstructive hydrocephalus ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary renal cell carcinoma pharyngitis pneumonia post-traumatic stress disorder progressive muscular atrophy psoriatic arthritis rheumatoid arthritis senile degeneration of brain sick sinus syndrome status epilepticus steatotic liver disease stomach cancer stomach carcinoma subacute delirium supratentorial primitive neuroectodermal tumor tethered spinal cord syndrome thyroid gland papillary carcinoma type 2 diabetes mellitus visual epilepsy
7358	UDP-glucose 6-dehydrogenase	UGDH Aliases: GDH UDP-GlcDH UDPGDH UGD uridine-diphospho glucose dehydrogenase	Homo sapiens (human)	Graves' disease Laron syndrome Zollinger-Ellison syndrome achondroplasia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cholangiocarcinoma developmental and epileptic encephalopathy 84 diarrhea enophthalmos giant cell glioblastoma giardiasis glioblastoma hepatocellular carcinoma high grade glioma hyperinsulinism hyperthyroidism hypoglycemia intrahepatic cholangiocarcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma obsolete exophthalmos orbital disease peripheral artery disease placental insufficiency primary hyperoxaluria thalassemia thyrotoxicosis
2582	UDP-galactose-4-epimerase	GALE Aliases: SDR1E1 UDP-glucose 4-epimerase short chain dehydrogenase/reductase family 1E, member 1	Homo sapiens (human)	Guillain-Barre syndrome Miller Fisher syndrome benign familial infantile epilepsy benign familial neonatal epilepsy benign neonatal seizures classic galactosemia cystinuria galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease stomach cancer stomach carcinoma thrombocytopenia tuberculosis

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