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	October 29, 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

Search results for "response to monosaccharide"

Displaying entries **1 - 25** of **733** in total

1

2

3

4

5

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
93	activin A receptor type 2B	ACVR2B	Homo sapiens (human)
114	adenylate cyclase 8	ADCY8	Homo sapiens (human)
285	angiopoietin 2	ANGPT2	Homo sapiens (human)
336	apolipoprotein A2	APOA2	Homo sapiens (human)
846	calcium sensing receptor	CASR	Homo sapiens (human)
847	catalase	CAT	Homo sapiens (human)	46,XY sex reversal 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 Barrett's esophagus Behcet's disease Bloom syndrome Burkitt lymphoma Carney complex Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Clostridium difficile colitis Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Crimean-Congo hemorrhagic fever Down syndrome Dubowitz syndrome Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Graves ophthalmopathy Graves' disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hailey-Hailey disease Hantavirus hemorrhagic fever with renal syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Kawasaki disease Langerhans-cell histiocytosis Leber hereditary optic neuropathy Marfan syndrome Meesmann corneal dystrophy Miles-Carpenter syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Raynaud disease Refsum disease Rett syndrome Reye syndrome Robinow syndrome Rothmund-Thomson syndrome Scheie syndrome Seckel syndrome Silver-Russell syndrome St. Louis encephalitis Sveinsson chorioretinal atrophy T-cell acute lymphoblastic leukemia Turner syndrome WAGR syndrome Werner syndrome Wernicke-Korsakoff syndrome Wilson disease Wolman disease X-linked Aarskog syndrome X-linked chronic granulomatous disease Zellweger syndrome Zika fever abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acatalasia acne acoustic neuroma acquired hyperkeratosis acrodermatitis actinic keratosis actinomycosis acute cholangitis acute intermittent porphyria acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adenosarcoma adrenal gland cancer adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome age related macular degeneration agenesis of the corpus callosum with peripheral neuropathy aggressive systemic mastocytosis agnosia alcohol dependence alcohol use disorder alcoholic liver cirrhosis allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis alpha 1-antitrypsin deficiency amnestic disorder amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anemia angioedema angle-closure glaucoma animal phobia aniridia ankylosing spondylitis anterior horn cell disease anterolateral myocardial infarction anteroseptal myocardial infarction anthracosilicosis anthracosis antisocial personality disorder anxiety disorder aortic aneurysm aortic disease aortic valve insufficiency aphthous stomatitis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis ascariasis ascaridiasis aspergillosis asphyxia neonatorum aspiration pneumonia aspiration pneumonitis asthma ataxia telangiectasia atherosclerosis atrial fibrillation 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 autism spectrum disorder autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cerebellar ataxia autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive Robinow syndrome 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 distal hereditary motor neuronopathy 1 azoospermia background diabetic retinopathy bacterial infectious disease bacterial pneumonia bacterial sepsis basal cell carcinoma benign mesothelioma bestrophinopathy beta thalassemia bile duct adenocarcinoma bile duct carcinoma bipolar disorder black piedra bladder carcinoma blood coagulation disease bone marrow cancer bone osteosarcoma brain cancer brain disease brain infarction brain ischemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma bronchopulmonary dysplasia bronchus cancer bronchus carcinoma byssinosis cancer carbamoyl phosphate synthetase I deficiency disease carcinoma cardiac arrest cardiomyopathy cardiovascular system disease cartilage-hair hypoplasia cataract cellular schwannoma central nervous system cancer central nervous system lymphoma central sleep apnea cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral malaria cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix disease cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood lymphoma childhood osteosarcoma cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chondrodysplasia-pseudohermaphroditism syndrome choriocarcinoma choroid plexus papilloma chromophobe renal cell carcinoma chronic closed-angle glaucoma chronic fatigue syndrome chronic granulomatous disease chronic kidney disease chronic myeloid leukemia chronic obstructive pulmonary disease chronic purulent otitis media chronic venous insufficiency clear cell renal cell carcinoma cleft palate coccidioidomycosis colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency congenital hemolytic anemia congenital hypothyroidism congestive heart failure corneal disease coronary artery disease coronary thrombosis cribriform carcinoma critical illness polyneuropathy cutaneous anthrax cutaneous leishmaniasis cutis laxa cystic fibrosis cystitis cystoid macular edema deficiency anemia degeneration of macula and posterior pole delusional disorder dengue disease denture stomatitis depressive disorder dermatitis developmental coordination disorder diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy diffuse large B-cell lymphoma diffuse scleroderma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal arthrogryposis duodenum cancer duodenum disease dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endometritis endomyocardial fibrosis eosinophilia-myalgia syndrome epidermolysis bullosa dystrophica epilepsy erysipelas erythrasma esophageal disease essential hypertension extramedullary plasmacytoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial hyperlipidemia familial mediterranean fever familial periodic paralysis favism female stress incontinence fibrillary astrocytoma fibromyalgia focal epilepsy fragile X syndrome gallbladder cancer gallbladder carcinoma gastric adenocarcinoma gastric ulcer gastritis gastroenteritis gastrointestinal system disease gemistocytic astrocytoma generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucocorticoid-remediable aldosteronism glucose intolerance goiter gonadal dysgenesis gonadoblastoma gonorrhea granular cell carcinoma granular corneal dystrophy 2 head and neck squamous cell carcinoma heart cancer heart disease hemiplegia hemochromatosis hemolytic-uremic syndrome hemopericardium hepatitis A hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hereditary elliptocytosis hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 5 hereditary spherocytosis type 1 hereditary spherocytosis herpes simplex high grade glioma histoplasmosis holoprosencephaly 1 holoprosencephaly homocystinuria hyperglycemia hyperhomocysteinemia hypertension hyperthyroidism hypertrophic cardiomyopathy hyperuricemia hypochromic anemia hypothalamic disease hypothyroidism idiopathic interstitial pneumonia ileitis ileocolitis immune system disease inclusion body myositis infantile Refsum disease inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease insulinoma intellectual disability interstitial nephritis intestinal disease intrahepatic cholangiocarcinoma intraocular lymphoma intrinsic asthma iron metabolism disease irritable bowel syndrome isolated cleft palate juvenile pilocytic astrocytoma juvenile rheumatoid arthritis keratitis keratoacanthoma keratoconjunctivitis keratoconus keratosis kernicterus due to isoimmunization kernicterus kidney cancer kidney disease kidney failure kidney hypertrophy kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer late onset Parkinson's disease lateral sclerosis learning disability lesion of sciatic nerve leukopenia lichen disease lichen planus lipid storage disease listeriosis liver cancer liver cirrhosis localized scleroderma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lymphoma lysosomal acid lipase deficiency macrocytic anemia macular corneal dystrophy macular degeneration macular retinal edema major depressive disorder mal de Meleda malaria male infertility malignant astrocytoma malignant mesothelioma marasmus mast-cell sarcoma melancholic depression melanoma melanotic neurilemmoma meningioma meningitis meningoencephalitis microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly microcytic anemia middle cerebral artery infarction migraine with aura migraine without aura mitral valve stenosis mixed glioma mixed oligodendroglioma-astrocytoma mood disorder motor neuron disease motor peripheral neuropathy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis multiple myeloma multiple sclerosis myelitis myelofibrosis myeloproliferative neoplasm myocardial infarction myocardial stunning myopathy myotonic dystrophy type 1 myxedema neonatal jaundice neovascular inflammatory vitreoretinopathy nephritis nephroblastoma nephrolithiasis nephrosis neurilemmoma neuroblastoma neurocirculatory asthenia neurodegenerative disease neurofibromatosis neuropathy neurotic disorder newborn respiratory distress syndrome nodular prostate non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive lung disease optic neuritis osteoarthritis osteoglophonic dysplasia osteonecrosis osteoporosis osteosarcoma otitis media ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary renal cell carcinoma papilloma parapsoriasis parathyroid gland disease parietal foramina partial motor epilepsy patent foramen ovale pemphigus pericardial effusion pericarditis perinatal necrotizing enterocolitis periodontal disease periodontitis peripheral nervous system disease peroxisomal disease peroxisome biogenesis disorder 1A peroxisome biogenesis disorder 7A peroxisome biogenesis disorder 8A personality disorder phenylketonuria pheochromocytoma phobic disorder photosensitive trichothiodystrophy phototoxic dermatitis pilocytic astrocytoma pituitary adenoma pityriasis rubra pilaris placenta cancer placental insufficiency plasmacytoma plexiform schwannoma pneumoconiosis pneumonia polycystic ovary syndrome polycythemia vera polyneuropathy post-traumatic stress disorder postinflammatory pulmonary fibrosis prediabetes syndrome preretinal fibrosis primary angle-closure glaucoma primary open angle glaucoma proctitis progeria progressive multifocal leukoencephalopathy progressive muscular atrophy proliferative diabetic retinopathy prostate cancer prostate carcinoma prostate disease prostatic adenoma protein-energy malnutrition protoplasmic astrocytoma pseudoxanthoma elasticum psoriasis pterygium pulmonary edema pulmonary embolism pulmonary emphysema pulmonary fibrosis purpura pustulosis of palm and sole pyelitis pyelonephritis pyoureter recessive dystrophic epidermolysis bullosa renal artery disease renal carcinoma renal cell carcinoma restrictive dermopathy reticulosarcoma retinal disease retinitis pigmentosa retinitis retinopathy of prematurity retrograde amnesia rheumatoid arthritis sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma scabies schizophrenia sciatic neuropathy scleroderma sebaceous carcinoma seborrheic dermatitis senile cataract sensorineural hearing loss sick sinus syndrome sickle cell anemia silent myocardial infarction situs inversus skin atrophy skin benign neoplasm skin cancer skin melanoma small intestine cancer social phobia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy specific phobia spinal muscular atrophy spinal stenosis spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spondylocarpotarsal synostosis syndrome sporotrichosis squamous cell carcinoma squamous cell papilloma status epilepticus steatotic liver disease stomach cancer stomach carcinoma stomach disease stomatitis subacute bacterial endocarditis subependymal giant cell astrocytoma superficial mycosis superior mesenteric artery syndrome suppurative otitis media sweat gland cancer systemic lupus erythematosus systemic scleroderma teratocarcinoma thrombocytopenia thrombophilia thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma toxic encephalopathy transient cerebral ischemia trigonitis tuberculosis tuberous sclerosis tubular adenocarcinoma 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 ulcerative colitis ulcerative stomatitis urea cycle disorder uremia ureteral obstruction uric acid nephrolithiasis urinary bladder cancer urticaria uterine corpus cancer uveoparotid fever varicocele variegate porphyria vascular disease vasomotor rhinitis vertebrobasilar insufficiency vestibular schwannomatosis viral infectious disease visual epilepsy vitiligo white piedra xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum yellow fever
1027	cyclin dependent kinase inhibitor 1B	CDKN1B	Homo sapiens (human)
1215	chymase 1	CMA1	Homo sapiens (human)
1277	collagen type I alpha 1 chain	COL1A1	Homo sapiens (human)
1285	collagen type IV alpha 3 chain	COL4A3	Homo sapiens (human)
1292	collagen type VI alpha 2 chain	COL6A2	Homo sapiens (human)
1293	collagen type VI alpha 3 chain	COL6A3	Homo sapiens (human)
1361	carboxypeptidase B2	CPB2	Homo sapiens (human)
1581	cytochrome P450 family 7 subfamily A member 1	CYP7A1 Aliases: cholesterol 7 alpha-monooxygenase cholesterol 7α-hydroxylase	Homo sapiens (human)	Aicardi-Goutieres syndrome Gerstmann-Straussler-Scheinker syndrome Gorham's disease Graves' disease acute monocytic leukemia acute myeloid leukemia acute myocardial infarction alcoholic hepatitis androgen insensitivity syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis biliary atresia cardiovascular system disease cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital bile acid synthesis defect 3 congenital bile acid synthesis defect coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism essential hypertension extrahepatic cholestasis familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia gallbladder cancer gallbladder carcinoma gallbladder disease gestational diabetes heart disease hepatitis hepatoblastoma hepatocellular carcinoma homocystinuria hypertension hyperthyroidism intrahepatic cholangiocarcinoma kwashiorkor large intestine cancer liver cancer liver disease marasmus metabolic dysfunction-associated steatohepatitis multiple sclerosis myocardial infarction neuromyelitis optica nutmeg liver nutrition disease obesity obsolete type 1 diabetes mellitus 9 osteomalacia placental insufficiency premature menopause primary biliary cholangitis primary ovarian insufficiency protein-energy malnutrition rickets silent myocardial infarction steatotic liver disease thyrotoxicosis tuberculosis 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
1636	angiotensin I converting enzyme	ACE Aliases: ACE1 CD143 peptidyl-dipeptidase A	Homo sapiens (human)	Alport syndrome 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 Balo concentric sclerosis Bannayan-Riley-Ruvalcaba syndrome Becker muscular dystrophy Behcet's disease Burkitt lymphoma CAKUT COVID-19 Chagas disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Clostridium difficile colitis Coronavirus infectious disease Cowden syndrome Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Duchenne muscular dystrophy Fabry disease Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease Goodpasture syndrome Graves' disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Henoch-Schoenlein purpura Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Kawasaki disease Keshan disease Kuhnt-Junius degeneration Langerhans-cell histiocytosis Leber hereditary optic neuropathy Lewy body dementia Marfan syndrome Meckel syndrome 8 Meckel syndrome Mycoplasma pneumoniae pneumonia Netherton syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Potter's syndrome Prinzmetal angina Raynaud disease Reye syndrome Richter's syndrome Senior-Loken syndrome Sjogren's syndrome St. Louis encephalitis T-cell acute lymphoblastic leukemia Takayasu's arteritis Werner syndrome Wilson disease X-linked dilated cardiomyopathy Zollinger-Ellison syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 ablepharon macrostomia syndrome acne acquired immunodeficiency syndrome acrodermatitis acromegaly actinic keratosis acute biphenotypic leukemia acute chest syndrome acute kidney failure acute leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute pancreatitis acute pyelonephritis adenocarcinoma adenoma adrenal gland cancer adrenal gland hyperfunction adrenoleukodystrophy adult fibrosarcoma adult lymphoma adult respiratory distress syndrome age related macular degeneration agenesis of the corpus callosum with peripheral neuropathy agnosia agoraphobia agranulocytosis alcohol dependence alcohol use disorder alcoholic cardiomyopathy alcoholic hepatitis alcoholic liver cirrhosis allergic asthma allergic contact dermatitis allergic disease allergic rhinitis alopecia areata alopecia alpha 1-antitrypsin deficiency alternating hemiplegia of childhood amnestic disorder amyloidosis amyotrophic lateral sclerosis anemia angioedema angioma serpiginosum ankylosing spondylitis anterolateral myocardial infarction anteroseptal myocardial infarction anthracosilicosis antisocial personality disorder antithrombin III deficiency anuria anxiety disorder aortic aneurysm aortic atherosclerosis aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arteriovenous malformation arthritis arthropathy asbestosis aseptic meningitis aspiration pneumonia aspiration pneumonitis asthma atherosclerosis atrial fibrillation atrioventricular block atrioventricular septal defect autistic disorder autoimmune disease autoimmune hepatitis 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 dominant polycystic kidney disease autosomal recessive congenital ichthyosis 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 autosomal recessive polycystic kidney disease background diabetic retinopathy bacterial infectious disease bacterial sepsis basal cell carcinoma berylliosis bestrophinopathy bicuspid aortic valve disease bile duct adenocarcinoma bile duct carcinoma bipolar disorder bone cancer bone disease bone marrow cancer borderline personality disorder brain disease brain infarction brain ischemia brain stem infarction breast cancer breast carcinoma breast fibrocystic disease bronchiolitis obliterans bronchus cancer bronchus carcinoma burning mouth syndrome campomelic dysplasia cancer cannabis abuse cannabis dependence capillary disease capillary hemangioma carcinoma cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis carpal tunnel syndrome cartilage disease cataract 32 multiple types cataract catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cavernous hemangioma celiac disease central gyrate choroidal dystrophy central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral atherosclerosis cerebral cavernous malformation 1 cerebral degeneration cerebral infarction cerebral malaria cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood leukemia childhood lymphoma childhood type dermatomyositis cholangiocarcinoma cholera cholestasis chondrocalcinosis chorioretinitis choroiditis chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease ciliary body disease clear cell renal cell carcinoma colitis collagen disease collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency complex partial epilepsy cone-rod dystrophy congenital central hypoventilation syndrome congenital diaphragmatic hernia congenital heart disease congenital hypothyroidism congenital muscular dystrophy congenital nongoitrous hypothyroidism 4 congestive heart failure connective tissue disease coronary aneurysm coronary artery disease coronary artery vasospasm coronary restenosis coronary stenosis coronary thrombosis craniometaphyseal dysplasia crescentic glomerulonephritis cribriform carcinoma critical illness polyneuropathy cystic fibrosis cystoid macular edema degeneration of macula and posterior pole dementia dental caries dentin caries depressive disorder dermatitis dermatomyositis diabetes mellitus diabetic angiopathy diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy diastolic heart failure diastrophic dysplasia dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of mental health disease of metabolism distal myopathy drug psychosis dry eye syndrome duodenum cancer dyschromatosis symmetrica hereditaria dysgerminoma of ovary dysthymic disorder eclampsia embryoma embryonal cancer encephalitis encephalomyelitis end stage renal disease endocarditis endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis enterocele epilepsy episodic kinesigenic dyskinesia 1 esophageal cancer esophageal carcinoma esophagitis essential hypertension essential thrombocythemia extrinsic allergic alveolitis exudative vitreoretinopathy 1 exudative vitreoretinopathy facioscapulohumeral muscular dystrophy familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial hypertrophic cardiomyopathy familial mediterranean fever familial nephrotic syndrome familial periodic paralysis fibromyalgia fibrosarcoma focal segmental glomerulosclerosis 1 focal segmental glomerulosclerosis 2 focal segmental glomerulosclerosis 5 focal segmental glomerulosclerosis 6 focal segmental glomerulosclerosis 7 focal segmental glomerulosclerosis 8 focal segmental glomerulosclerosis 9 focal segmental glomerulosclerosis follicular adenoma frontotemporal dementia fundus albipunctatus gallbladder adenocarcinoma gallbladder cancer gallbladder carcinoma gallbladder disease gastric ulcer gastritis gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gastrointestinal system disease generalized anxiety disorder generalized atherosclerosis germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomerulosclerosis glucose intolerance glycogen storage disease II glycogen storage disease V granular cell carcinoma granular corneal dystrophy 2 granulomatosis with polyangiitis heart cancer heart disease heart valve disease hematologic cancer hemochromatosis hemopericardium hepatitis A hepatitis B hepatitis C hepatitis hepatocellular carcinoma hereditary angioedema hereditary hemorrhagic telangiectasia hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spherocytosis type 1 hereditary spherocytosis hiatus hernia high grade glioma human immunodeficiency virus infectious disease hydronephrosis hyperandrogenism hypercalcemia hyperglycemia hyperhomocysteinemia hyperinsulinism hyperparathyroidism hyperpituitarism hypersensitivity vasculitis hypertension hypertensive heart disease hyperthyroidism hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypoplastic left heart syndrome hypothyroidism ichthyosis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis idiopathic scoliosis ileitis ileocolitis immune system disease impotence inappropriate ADH syndrome infective endocarditis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inflammatory myofibroblastic tumor intermediate coronary syndrome intermittent claudication intermittent explosive disorder interstitial lung disease interstitial nephritis intestinal disease intracranial aneurysm intracranial arteriosclerosis intrahepatic cholangiocarcinoma intrahepatic cholestasis of pregnancy intrinsic asthma iris disease iron metabolism disease irritable bowel syndrome keratoconjunctivitis sicca keratosis follicularis kidney cancer kidney disease kidney failure kidney hypertrophy kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer left bundle branch hemiblock leiomyoma leukemia leukostasis limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphangioleiomyomatosis lymphoma lymphopenia macrocytic anemia macular degeneration macular retinal edema major depressive disorder malaria male infertility malignant hypertension marasmus megacystis-microcolon-intestinal hypoperistalsis syndrome melancholic depression melanoma membranous glomerulonephritis meningoencephalitis mevalonic aciduria microcephaly microcystic adenoma microglandular adenosis microinvasive gastric cancer microphthalmia middle cerebral artery infarction migraine with aura migraine without aura migraine mitral valve disease mitral valve insufficiency mitral valve prolapse mitral valve stenosis mixed glioma mixed sleep apnea mongolian spot mood disorder morbid obesity motor peripheral neuropathy multiple endocrine neoplasia type 2A multiple myeloma multiple sclerosis multiple system atrophy muscular dystrophy musculoskeletal system disease myelitis myelodysplastic syndrome myelofibrosis myeloproliferative neoplasm myocardial infarction myocarditis myofibrillar myopathy 1 myofibrillar myopathy 3 myofibroma myopathy myositis myotonic dystrophy type 1 myotonic dystrophy type 2 myxedema narcolepsy nasopharynx carcinoma neovascular inflammatory vitreoretinopathy nephritis nephrocalcinosis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis nephrotic syndrome type 1 nephrotic syndrome type 2 nephrotic syndrome nervous system disease neurocirculatory asthenia neurodegenerative disease neuromuscular disease neuromyelitis optica neuropathy neurotic disorder neutropenia newborn respiratory distress syndrome nicotine dependence nodular prostate non-Hodgkin lymphoma non-arteritic anterior ischemic optic neuropathy nonpapillary renal cell carcinoma normal pressure hydrocephalus nutmeg liver nutrition disease nutritional optic neuropathy obesity obsolete Cushing's syndrome 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 obsolete chronobiology disease obsolete congenital ichthyosiform erythroderma obsolete constipation obsolete eye and adnexa disease obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea ocular hypotension oculopharyngeal muscular dystrophy oligohydramnios open-angle glaucoma osteitis fibrosa osteoarthritis osteomalacia osteonecrosis osteoporosis otosclerosis ovarian cancer ovarian carcinoma pancreas disease pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma pancreatitis panic disorder panuveitis papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis patent ductus arteriosus pemphigus vulgaris pemphigus peptic esophagitis peptic ulcer disease pericardial effusion perinatal necrotizing enterocolitis periodontal disease periodontitis peripheral artery disease peripheral nervous system disease peripheral vascular disease periventricular leukomalacia personality disorder pheochromocytoma phobic disorder phosphorus metabolism disease placental insufficiency plasmacytoma pneumonia polyarteritis nodosa polycystic kidney disease 1 polycystic kidney disease 4 polycystic ovary syndrome polycythemia vera polycythemia polyneuropathy portal hypertension post-traumatic stress disorder posterior uveitis postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome pre-eclampsia pre-malignant neoplasm prediabetes syndrome premature ejaculation primary biliary cholangitis primary hyperaldosteronism primary hyperparathyroidism primary open angle glaucoma primary ovarian insufficiency primary polycythemia primary pulmonary hypertension progeria progressive muscular atrophy progressive supranuclear palsy proliferative diabetic retinopathy prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency protein-energy malnutrition proteinuria pseudoxanthoma elasticum psoriasis psoriatic arthritis psychologic dyspareunia psychotic disorder pterygium pulmonary edema pulmonary embolism pulmonary emphysema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole pyelitis pyelonephritis pyoureter pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rapidly progressive glomerulonephritis rectal benign neoplasm rectum adenocarcinoma rectum cancer red-green color blindness reflex sympathetic dystrophy renal artery disease renal artery obstruction renal carcinoma renal cell carcinoma renal fibrosis renal hypertension renal infectious disease renal osteodystrophy renovascular hypertension respiratory syncytial virus infectious disease restrictive cardiomyopathy 1 restrictive cardiomyopathy reticulosarcoma retinal disease retinal vein occlusion retinitis pigmentosa retinitis retinopathy of prematurity rheumatoid arthritis rhinitis rickets rippling muscle disease 2 sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleritis scleroderma seasonal affective disorder seborrheic keratosis seminoma sensorineural hearing loss severe acute respiratory syndrome severe congenital neutropenia sexual dysfunction sick sinus syndrome sickle cell anemia silent myocardial infarction silicosis situs inversus skin atrophy skin benign neoplasm skin cancer skin disease skin melanoma sleep apnea small intestine cancer somatization disorder somatoform disorder speech-language disorder-1 spondyloarthropathy spondylosis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis subacute sclerosing panencephalitis substance abuse substance-related disorder synovial sarcoma systemic lupus erythematosus systemic scleroderma systolic heart failure telangiectasis temporal lobe epilepsy testicular cancer testicular germ cell cancer testis seminoma tetralogy of Fallot thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma thyrotoxicosis tongue squamous cell carcinoma toxic shock syndrome transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue trypanosomiasis tuberculosis tuberculous pneumothorax tuberous sclerosis 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 type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis uremia ureteral obstruction urinary system benign neoplasm urinary system cancer urinary tract obstruction urticaria uterine corpus cancer uterine fibroid uveitis uveoparotid fever vascular dementia vascular disease vasculitis vasomotor rhinitis vertebrobasilar insufficiency vesicoureteral reflux viral infectious disease viral meningitis viral pneumonia visual epilepsy vitiligo xerophthalmia
1958	early growth response 1	EGR1	Homo sapiens (human)
1967	eukaryotic translation initiation factor 2B subunit alpha	EIF2B1	Homo sapiens (human)
2030	solute carrier family 29 member 1 (Augustine blood group)	SLC29A1	Homo sapiens (human)
2081	endoplasmic reticulum to nucleus signaling 1	ERN1 Aliases: IRE1 IRE1P Serine/threonine-protein kinase/endoribonuclease IRE1 inositol-requiring enzyme 1	Homo sapiens (human)
2309	forkhead box O3	FOXO3	Homo sapiens (human)
2621	growth arrest specific 6	GAS6	Homo sapiens (human)
2626	GATA binding protein 4	GATA4	Homo sapiens (human)
2645	glucokinase	GCK Aliases: HK4 hexokinase 4	Homo sapiens (human)	Chagas disease Fanconi anemia complementation group C Fanconi anemia Laron syndrome Marfan syndrome Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute chest syndrome adult-onset Still's disease agnosia apraxia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bronchus cancer bronchus carcinoma cancer cardiovascular system disease chronic fatigue syndrome congenital heart disease congenital ptosis coronary artery disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism embryoma encephalitis encephalomyelitis endocrine pancreas disease epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperinsulinemic hypoglycemia 3 generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease heart disease hepatocellular carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia hypoglycemic coma immune system disease insulinoma intellectual disability kidney disease learning disability leishmaniasis liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young type 3 maturity-onset diabetes of the young myelitis myotonic dystrophy type 1 myotonic dystrophy type 2 neonatal diabetes nephritis nephrosis neuropathy nutmeg liver obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 osteoarthritis pancreatic cancer pancreatic carcinoma peripheral nervous system disease permanent neonatal diabetes mellitus placental insufficiency polyneuropathy prediabetes syndrome progeria prostate cancer prostate carcinoma ptosis pyoureter retinal disease retinitis rheumatoid arthritis sensorineural hearing loss situs inversus steatotic liver disease syndromic X-linked intellectual disability 94 systemic lupus erythematosus transient neonatal diabetes mellitus trypanosomiasis tuberous sclerosis 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 urea cycle disorder visceral leishmaniasis visual epilepsy
2696	gastric inhibitory polypeptide receptor	GIPR	Homo sapiens (human)
2729	glutamate-cysteine ligase catalytic subunit	GCLC	Homo sapiens (human)	cataract colorectal cancer cystic fibrosis glutamate-cysteine ligase deficiency hemolytic anemia liver cirrhosis myocardial infarction pulmonary emphysema

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