GlyCosmos Portal

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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 **1051 - 1075** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
170384	fucosyltransferase 11	FUT11 Aliases: MGC33202 alpha (1,3) fucosyltransferase	Homo sapiens (human)	bronchus cancer bronchus carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stomach cancer
55753	oxoglutarate dehydrogenase L	OGDHL Aliases: FLJ10851	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 Pick's disease Reye syndrome Yoon-Bellen neurodevelopmental syndrome breast cancer cancer cerebral degeneration colorectal cancer colorectal carcinoma embryoma eosinophilic esophagitis hepatocellular carcinoma large intestine cancer liver cancer oxoglutarate dehydrogenase deficiency pancreatic cancer pancreatic carcinoma
414	arylsulfatase D	ARSD Aliases: ASD	Homo sapiens (human)	Asperger syndrome Bannayan-Riley-Ruvalcaba syndrome Beckwith-Wiedemann syndrome CLOVES syndrome Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome Cowden syndrome Down syndrome Dubowitz syndrome Lown-Ganong-Levine syndrome Marfan syndrome Mowat-Wilson 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 Perlman syndrome Prader-Willi syndrome Rett syndrome Richter's syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Sotos syndrome Williams-Beuren syndrome Wolff-Parkinson-White syndrome X-linked Aarskog syndrome acute kidney tubular necrosis acute myeloid leukemia acute promyelocytic leukemia adult respiratory distress syndrome alexia amnestic disorder aniridia anxiety disorder aortic valve disease 1 aortic valve disease 2 aortic valve stenosis argininosuccinic aciduria arteriosclerotic cardiovascular disease atherosclerosis 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 atrioventricular block atrioventricular septal defect attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bicuspid aortic valve disease breast cancer breast carcinoma buphthalmos cardiomyopathy cardiovascular system disease cerebral palsy chondrodysplasia-pseudohermaphroditism syndrome chronic lymphocytic leukemia citrullinemia communication disorder conduct disorder congenital heart disease congestive heart failure coronary artery disease depressive disorder developmental coordination disorder disease of mental health dyslexia dysthymic disorder eating disorder endocarditis endometriosis of uterus endometriosis endomyocardial fibrosis epilepsy essential hypertension excessive tearing familial hypertrophic cardiomyopathy fragile X syndrome generalized anxiety disorder glaucoma heart disease hemiplegia hydrophthalmos hyperargininemia hypertension hypertrophic cardiomyopathy hypospadias immune system disease infective endocarditis intellectual disability juvenile glaucoma lacrimal apparatus disease language disorder learning disability major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia neurotic disorder newborn respiratory distress syndrome nicotine dependence obesity obsolete melancholia patent ductus arteriosus patent foramen ovale phobic disorder polycystic ovary syndrome post-traumatic stress disorder primary open angle glaucoma psychotic disorder pulmonary valve stenosis retrograde amnesia schizophrenia sclerocornea situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy subacute bacterial endocarditis substance abuse substance-related disorder supravalvular aortic stenosis syndromic X-linked intellectual disability 94 tuberous sclerosis ventricular septal defect visual epilepsy
3373	hyaluronidase 1	HYAL1 Aliases: HYAL-1 LUCA1	Homo sapiens (human)	Laron syndrome achondroplasia arthritis arthropathy bladder carcinoma breast cancer breast carcinoma cancer carcinoma central nervous system cancer chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma embryoma endometrial cancer endometrial carcinoma gliosarcoma head and neck cancer head and neck squamous cell carcinoma high grade glioma juvenile rheumatoid arthritis large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer lung benign neoplasm lung cancer lung non-small cell carcinoma lung small cell carcinoma lysosomal storage disease mixed glioma mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IX mucopolysaccharidosis VI mucopolysaccharidosis osteoarthritis osteochondrodysplasia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma primary pulmonary hypertension prostate cancer prostate carcinoma pulmonary hypertension sarcomatoid carcinoma skin disease squamous cell carcinoma tongue squamous cell carcinoma urinary bladder cancer uterine corpus cancer
221937	forkhead box K1	FOXK1	Homo sapiens (human)
5648	MBL associated serine protease 1	MASP1 Aliases: C4/C2 activating component of Ra-reactive factor MAP-1 MASP MASP-3 Map44 mannose-binding lectin-associated serine protease 1	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC 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 Bloch-Sulzberger syndrome Klippel-Feil syndrome Lewy body dementia Marfan syndrome Pick's disease Reye syndrome acute myocardial infarction age related macular degeneration amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 6 arthritis arthropathy 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 atypical hemolytic-uremic syndrome bacterial infectious disease bacterial sepsis blepharophimosis blindness cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cleft lip cleft palate cleidocranial dysplasia congenital ptosis coronary thrombosis craniosynostosis cryptorchidism cystic fibrosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis disseminated intravascular coagulation esophagus squamous cell carcinoma gallbladder disease glaucoma glomerulonephritis heart disease hemolytic-uremic syndrome hepatitis C humeroradial synostosis hydronephrosis hypomelanosis of Ito inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 intellectual disability isolated cleft palate kidney disease kidney failure learning disability liver cirrhosis liver disease lung squamous cell carcinoma lupus erythematosus macular degeneration microcephaly multiple sclerosis myocardial infarction nephritis omphalocele patent ductus arteriosus patent foramen ovale placental insufficiency prostate cancer prostate carcinoma ptosis pulmonary tuberculosis purpura fulminans radioulnar synostosis rheumatoid arthritis scoliosis sensorineural hearing loss silent myocardial infarction situs inversus spina bifida occulta spondylolisthesis squamous cell carcinoma systemic lupus erythematosus tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tuberous sclerosis type 2 diabetes mellitus umbilical hernia uremia vascular dementia ventricular septal defect
5471	phosphoribosyl pyrophosphate amidotransferase	PPAT Aliases: GPAT PRAT	Homo sapiens (human)	alcohol dependence alcohol use disorder breast cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatoblastoma hepatocellular carcinoma liver cancer ovarian cancer ovarian carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma
3420	isocitrate dehydrogenase (NAD(+)) 3 non-catalytic subunit beta	IDH3B Aliases: RP46	Homo sapiens (human)	Zollinger-Ellison syndrome bipolar disorder blindness cataract cone-rod dystrophy congenital nystagmus corneal disease diabetes mellitus dissociated nystagmus early infantile epileptic encephalopathy eye disease fundus albipunctatus fundus dystrophy glaucoma hidradenitis suppurativa hidradenitis hyperinsulinism hypogonadism intellectual disability keratoconus learning disability obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus pompholyx retinitis pigmentosa 46 retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma type 2 diabetes mellitus
124912	sperm acrosome associated 3	SPACA3 Aliases: ALLP17 CT54 LYC3 LYZL3 SLLP1 cancer/testis antigen 54 sperm lyzozyme-like acrosomal protein 1	Homo sapiens (human)	acute myeloid leukemia cancer hematologic cancer seminoma testicular cancer testis seminoma
131544	crystallin beta-gamma domain containing 3	CRYBG3 Aliases: DKFZp667G2110	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer embryoma lung cancer lung carcinoma
93210	post-GPI attachment to proteins phospholipase 3	PGAP3 Aliases: CAB2 MGC9753 PER1 PP1498 post-GPI attachment to proteins 3	Homo sapiens (human)	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 4 inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
2592	galactose-1-phosphate uridylyltransferase	GALT	Homo sapiens (human)	acquired immunodeficiency syndrome agnosia androgen insensitivity syndrome bacterial sepsis blood coagulation disease cancer cataract cerebellar ataxia cerebellar disease classic galactosemia cystinuria diabetic cataract diarrhea disease of metabolism endometriosis of uterus endometriosis galactokinase deficiency galactose epimerase deficiency galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatocellular carcinoma human immunodeficiency virus infectious disease hypoglycemia hypogonadism inherited metabolic disorder intellectual disability kwashiorkor lactic acidosis learning disability liver cancer liver cirrhosis liver disease marasmus neonatal jaundice nutrition disease osteoporosis ovarian cancer ovarian carcinoma premature menopause primary ovarian insufficiency protein-energy malnutrition proteinuria speech-language disorder-1 trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
10020	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	GNE Aliases: Uae1 bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	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 Bell's palsy GNE myopathy Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Paget's disease of bone Pick's disease Reye syndrome X-linked myopathy with excessive autophagy Zika fever amnestic disorder attention deficit hyperactivity disorder autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer cardiomyopathy cerebral degeneration cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital central hypoventilation syndrome congenital hypothyroidism dementia distal myopathy endomyocardial fibrosis epilepsy esophagitis facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis frontotemporal dementia gastroesophageal reflux disease hypertrophic cardiomyopathy hypothyroidism inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 inclusion body myositis inguinal hernia intrahepatic cholangiocarcinoma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis muscular dystrophy myopathy myositis myxedema neuromuscular disease nonpapillary renal cell carcinoma obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive sleep apnea oculopharyngeal muscular dystrophy pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis renal carcinoma renal cell carcinoma retrograde amnesia sarcomatoid renal cell carcinoma scoliosis sialuria sleep apnea thrombocytopenia tibial muscular dystrophy visual epilepsy
2821	glucose-6-phosphate isomerase	GPI Aliases: AMF NLK	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 Cockayne syndrome Cornelia de Lange syndrome Creutzfeldt-Jakob disease Down syndrome Dubowitz 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 Pick's disease Plasmodium vivax malaria Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adult fibrosarcoma adult lymphoma alternating hemiplegia of childhood anemia antiphospholipid syndrome aplastic anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrophic gastritis atypical hemolytic-uremic syndrome autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome benign mesothelioma blastomycosis bone osteosarcoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system disease central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood lymphoma childhood osteosarcoma cholecystitis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common cold congenital diaphragmatic hernia congenital disorder of glycosylation congenital hemolytic anemia congenital nonspherocytic hemolytic anemia coronary artery disease coronary thrombosis cystinuria depressive disorder diabetes mellitus diabetic ketoacidosis differentiated thyroid gland carcinoma diffuse large B-cell lymphoma dysthymic disorder dystonia embryoma encephalitis encephalomyelitis endocarditis endometrial cancer endometrial carcinoma essential hypertension essential thrombocythemia familial retinoblastoma favism female stress incontinence fetal erythroblastosis fibrosarcoma focal hand dystonia galactosemia generalized dystonia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease head and neck squamous cell carcinoma heart disease hematologic cancer hemoglobinopathy hemolytic anemia hemolytic-uremic syndrome hepatitis B hepatitis hepatocellular carcinoma hereditary elliptocytosis high grade glioma human immunodeficiency virus infectious disease hypertension immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease infective endocarditis inflammatory and toxic neuropathy influenza intellectual disability intracranial embolism large intestine cancer learning disability leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lupus erythematosus lymphoma macrocytic anemia major depressive disorder malignant hyperthermia malignant mesothelioma melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia migraine mixed glioma multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction neonatal anemia neonatal jaundice nervous system disease neurogenic arthropathy neuromuscular disease neurotic disorder nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatitis pancytopenia papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis paroxysmal nocturnal hemoglobinuria peeling skin syndrome placental insufficiency platelet-type bleeding disorder 3 pre-eclampsia primary immunodeficiency disease primary pulmonary hypertension prion disease pure red-cell aplasia renal carcinoma renal cell carcinoma respiratory syncytial virus infectious disease retinoblastoma rheumatoid arthritis sarcomatoid renal cell carcinoma scleroderma silent myocardial infarction skin atrophy steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis syndromic X-linked intellectual disability Snyder type syndromic intellectual disability synovitis systemic lupus erythematosus systemic scleroderma tenosynovitis thrombophilia thrombotic thrombocytopenic purpura thyroid gland anaplastic carcinoma thyroid gland papillary carcinoma trilateral retinoblastoma 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 uterine corpus cancer vascular dementia vascular disease viral infectious disease von Willebrand's disease
5164	pyruvate dehydrogenase kinase 2	PDK2	Homo sapiens (human)
3291	hydroxysteroid 11-beta dehydrogenase 2	HSD11B2 Aliases: SDR9C3 short chain dehydrogenase/reductase family 9C, member 3	Homo sapiens (human)	ACTH-secreting pituitary adenoma Bartter disease Clostridium difficile colitis Conn's syndrome Crohn's colitis Crohn's disease Kawasaki disease Laron syndrome Liddle syndrome Waterhouse-Friderichsen syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal cortex cancer adrenal gland hyperfunction adult respiratory distress syndrome alcohol dependence alcohol use disorder allergic asthma amnestic disorder anorexia nervosa anxiety disorder apparent mineralocorticoid excess syndrome arthritis arthropathy asphyxia neonatorum asthma atrial fibrillation autoimmune hepatitis bacterial sepsis bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer cardiac arrest cardiovascular system disease cerebral infarction cerebrotendinous xanthomatosis cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia childhood osteosarcoma choriocarcinoma chromophobe renal cell carcinoma chronic ethmoiditis chronic kidney disease chronic sphenoidal sinusitis clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital adrenal hyperplasia coronary thrombosis cystic fibrosis depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism eclampsia ectopic Cushing syndrome embryoma endemic goiter endometriosis of uterus endometriosis essential hypertension familial nephrotic syndrome fetal alcohol spectrum disorder follicular adenoma follicular lymphoma generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance heart disease hepatitis hepatocellular carcinoma hereditary breast ovarian cancer syndrome hypercalcemia hypertension hypertensive retinopathy hypokalemia immune system disease inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder intrinsic asthma irritable bowel syndrome kidney disease kidney failure large intestine cancer leprosy leukemia lipoid nephrosis liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma microcystic adenoma mood disorder myocardial infarction nephritis nephrocalcinosis nephrosis nephrotic syndrome neurocirculatory asthenia newborn respiratory distress syndrome obesity obsolete Cushing's syndrome obsolete type 1 diabetes mellitus 9 osteomalacia osteoporosis osteosarcoma ovarian cancer ovarian carcinoma papillary adenoma papillary renal cell carcinoma phobic disorder phosphorus metabolism disease pituitary adenoma pituitary cancer pituitary carcinoma pituitary-dependent Cushing's disease placenta cancer placenta disease placental insufficiency polycystic ovary syndrome pre-eclampsia prediabetes syndrome primary hyperaldosteronism pyoureter renal carcinoma renal cell carcinoma retrograde amnesia rheumatoid arthritis rickets sarcomatoid renal cell carcinoma schizophrenia silent myocardial infarction skin benign neoplasm skin cancer skin carcinoma skin melanoma skin squamous cell carcinoma stomach cancer stomach carcinoma substance abuse substance-related disorder substernal goiter trichohepatoenteric syndrome 1 trichohepatoenteric syndrome 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 ureteral obstruction
55501	carbohydrate sulfotransferase 12	CHST12 Aliases: C4S-2 C4ST2 chondroitin 4-sulfotransferase 2	Homo sapiens (human)	hypertension lupus erythematosus systemic lupus erythematosus
257202	glutathione peroxidase 6	GPX6 Aliases: selenoprotein GPX6	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease breast cancer depressive disorder lung squamous cell carcinoma major depressive disorder melancholic depression obsolete melancholia ovarian cancer ovarian carcinoma
2877	glutathione peroxidase 2	GPX2 Aliases: GSHPX-GI selenoprotein GPX2	Homo sapiens (human)	46,XY sex reversal Barrett's esophagus 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 adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervical adenocarcinoma cervical cancer cervix carcinoma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal adenoma colorectal cancer colorectal carcinoma embryoma follicular adenoma gastroenteritis hepatitis C hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma microcystic adenoma motor peripheral neuropathy nasopharynx carcinoma obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum pancreatic cancer pancreatic carcinoma papillary adenoma prostate cancer prostate carcinoma rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma stomach cancer stomach carcinoma transitional cell carcinoma ulcerative colitis urinary bladder cancer
1486	chitobiase	CTBS Aliases: di-N-acetylchitobiase	Homo sapiens (human)	Clouston syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer liver cancer progressive muscular atrophy prostate cancer prostate carcinoma ulcerative colitis vasomotor rhinitis
8898	myotubularin related protein 2	MTMR2 Aliases: KIAA1073 phosphatidylinositol-3-phosphatase phosphoinositide-3-phosphatase	Homo sapiens (human)	Bell's palsy 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 3 Charcot-Marie-Tooth disease type 4 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 agenesis of the corpus callosum with peripheral neuropathy agnosia axonal neuropathy cancer centronuclear myopathy X-linked centronuclear myopathy clubfoot congenital structural myopathy demyelinating polyneuropathy developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis glaucoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 motor peripheral neuropathy myopathy neurodegenerative disease neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease polyneuropathy scoliosis sensory peripheral neuropathy stomach cancer stomach carcinoma
56965	poly(ADP-ribose) polymerase family member 6	PARP6 Aliases: ARTD17 pART17	Homo sapiens (human)	breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer
4706	NADH:ubiquinone oxidoreductase subunit AB1	NDUFAB1 Aliases: ACP ACP1 FASN2A SDAP acyl carrier protein, mitochondrial complex I SDAP subunit	Homo sapiens (human)	Alzheimer's disease HCL-V Lynch syndrome Marfan syndrome Richter's syndrome Wilson disease X-linked dilated cardiomyopathy actinic keratosis adamantinous craniopharyngioma adult lymphoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ataxic cerebral palsy atherosclerosis brain cancer cancer central nervous system lymphoma central retinal vein occlusion cerebral infarction cerebrovascular disease childhood lymphoma chronic lymphocytic leukemia congenital hemolytic anemia congestive heart failure coronary artery disease craniopharyngioma cystinuria dementia dental caries dentin sensitivity 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 embryoma endometrial cancer endometrial carcinoma favism galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease gonorrhea hairy cell leukemia hemochromatosis hereditary elliptocytosis iron metabolism disease lymphoma neurodegeneration with brain iron accumulation neurodegenerative disease nutmeg liver obesity obsolete ymphosarcoma osteoporosis papillary craniopharyngioma root caries situs inversus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tuberous sclerosis uterine corpus cancer
51548	sirtuin 6	SIRT6	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 Clouston syndrome Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Kaposi's sarcoma Laron syndrome Marfan syndrome Pick's disease Reye syndrome Werner syndrome achondroplasia actinic keratosis acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma adrenoleukodystrophy alcoholic hepatitis allergic asthma amyotrophic lateral sclerosis anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis bacterial sepsis basal cell carcinoma bladder carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood leukemia childhood osteosarcoma chromophobe renal cell carcinoma chronic apical periodontitis chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary 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 coronary thrombosis cutaneous fibrous histiocytoma degenerative disc disease dengue disease depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma essential hypertension exanthem gallbladder disease gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance head and neck squamous cell carcinoma heart disease hematologic cancer hepatitis hepatocellular carcinoma hidradenoma high grade glioma hyperglycemia hypertension hypoglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis intrinsic asthma keratitis keratoconjunctivitis kidney disease kidney hypertrophy large intestine cancer leukemia lipoma liver cancer liver carcinoma liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia major depressive disorder melancholic depression melanoma metabolic dysfunction-associated steatotic liver disease microphthalmia mixed glioma multiple myeloma myelitis myocardial infarction myotonic dystrophy type 1 nasopharynx carcinoma nephritis nephrosis neuroblastoma neurodegenerative disease neurotic disorder nonpapillary renal cell carcinoma nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma periapical periodontitis phobic disorder pleomorphic lipoma postinflammatory pulmonary fibrosis prediabetes syndrome progeria progressive muscular atrophy prostate cancer prostate carcinoma psoriatic arthritis pulmonary fibrosis pulpitis pyoureter renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma seborrheic keratosis silent myocardial infarction situs inversus skin benign neoplasm skin cancer skin disease skin melanoma skin papilloma skin squamous cell carcinoma skin tag sporadic breast cancer squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma syringoma thyroid gland papillary carcinoma tongue squamous cell carcinoma transient cerebral ischemia transitional cell carcinoma tuberculosis 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 urinary bladder cancer uterine corpus cancer vertebrobasilar insufficiency viral infectious disease yellow fever
5298	phosphatidylinositol 4-kinase beta	PI4KB Aliases: PI4K-BETA pi4K92	Homo sapiens (human)	EAST syndrome autosomal dominant nonsyndromic deafness hepatitis C severe acute respiratory syndrome

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