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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 **351 - 375** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
3032	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta	HADHB Aliases: MTPB mitochondrial trifunctional protein, beta subunit	Homo sapiens (human)	Alzheimer's 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 Norum disease Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy agnosia beta-ketothiolase deficiency breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease cholestasis choreaacanthocytosis clubfoot colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure critical illness polyneuropathy developmental coordination disorder 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 endomyocardial fibrosis epilepsy familial hyperlipidemia familial periodic paralysis fibromyalgia fundus albipunctatus heart disease hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hypercalcemia hypertrophic cardiomyopathy hypolipoproteinemia hypoparathyroidism inflammatory and toxic neuropathy intellectual disability lactic acidosis large intestine cancer learning disability lipid metabolism disorder melanoma meningoencephalitis mitochondrial metabolism disease mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse motor peripheral neuropathy myoglobinuria myopathy myositis nephrocalcinosis neuropathy obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum peripheral nervous system disease phosphorus metabolism disease placental insufficiency polydactyly polyneuropathy prostate adenocarcinoma prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinitis pigmentosa sick sinus syndrome skin melanoma steatotic liver disease tricuspid valve insufficiency urea cycle disorder visual epilepsy
79947	dehydrodolichyl diphosphate synthase subunit	DHDDS Aliases: DS FLJ13102 HDS RP59 hCIT	Homo sapiens (human)	Alzheimer's disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Dubowitz syndrome Ehrlich tumor carcinoma Laron 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 Patau syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome Weissenbacher-Zweymuller syndrome X-linked Aarskog syndrome Zollinger-Ellison syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult medulloblastoma adult oligodendroglioma agranulocytosis amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bladder carcinoma blepharospasm blindness bone osteosarcoma brain stem glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carnitine palmitoyltransferase II deficiency cataract central nervous system cancer central nervous system lymphoma cerebral degeneration cervical squamous cell carcinoma childhood medulloblastoma childhood oligodendroglioma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital diaphragmatic hernia corneal disease cribriform carcinoma cryptorchidism decubitus ulcer dementia depressive disorder developmental delay and seizures with or without movement abnormalities diarrhea dysthymic disorder dystonia early myoclonic encephalopathy embryoma endometrial cancer endometrial carcinoma epilepsy esophagus squamous cell carcinoma focal hand dystonia fundus albipunctatus giant cell glioblastoma glaucoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma hiatus hernia high grade glioma hyperinsulinism hypoglycemia hypogonadism inflammatory bowel disease 1 inflammatory bowel disease islet cell tumor keratoconus kidney failure large intestine cancer leukopenia lingual-facial-buccal dyskinesia liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma neuroblastoma neurofibromatosis 1 neurofibromatosis neurotic disorder neutropenia obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma oligodendroglioma ophthalmoplegia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic endocrine carcinoma papillary renal cell carcinoma pathological gambling progressive muscular atrophy prostate cancer prostate carcinoma psychotic disorder pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal degeneration retinitis pigmentosa 59 retinitis pigmentosa rippling muscle disease 2 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe congenital neutropenia squamous cell carcinoma squamous cell neoplasm status epilepticus steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder thyroid gland medullary carcinoma tooth agenesis tubular adenocarcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer varicocele visual epilepsy
56994	choline phosphotransferase 1	CHPT1 Aliases: CPT1 phosphatidylcholine synthesizing enzyme	Homo sapiens (human)	Alzheimer's disease Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease 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 Patau syndrome Pearson syndrome Prader-Willi syndrome Robinow syndrome Schimke immuno-osseous dysplasia Seckel syndrome Silver-Russell syndrome Weissenbacher-Zweymuller syndrome X-linked Aarskog syndrome adenocarcinoma adenoma adult medulloblastoma agranulocytosis attention deficit hyperactivity disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome beta thalassemia bladder carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma carnitine palmitoyltransferase II deficiency carpal tunnel syndrome 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 central nervous system cancer central nervous system lymphoma cervical squamous cell carcinoma childhood medulloblastoma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congestive heart failure cribriform carcinoma decubitus ulcer depressive disorder diabetes mellitus diarrhea diverticulitis dysthymic disorder embryoma endocarditis endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma essential hypertension follicular adenoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis C hepatitis hepatocellular carcinoma hiatus hernia high grade glioma hypertension hypoglycemia infective endocarditis inflammatory bowel disease 1 inflammatory bowel disease islet cell tumor large intestine cancer leukopenia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma mixed glioma multiple myeloma neuroblastoma neurotic disorder neutropenia obesity obsolete melancholia obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic endocrine carcinoma papillary adenoma papillary renal cell carcinoma pathological gambling placental insufficiency post-traumatic stress disorder primary pulmonary hypertension prostate cancer prostate carcinoma psychotic disorder pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe congenital neutropenia sick sinus syndrome squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subacute bacterial endocarditis substance abuse substance-related disorder systemic primary carnitine deficiency disease thalassemia thyroid gland medullary carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer varicocele very long chain acyl-CoA dehydrogenase deficiency
10195	ALG3 alpha-1,3- mannosyltransferase	ALG3 Aliases: CDGS4 D16Ertd36e NOT56L Not56 carbohydrate deficient glycoprotein syndrome type IV dol-P-Man dependent alpha-1,3- mannosyltransferase dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	Homo sapiens (human)	Alzheimer's disease Creutzfeldt-Jakob disease acute myeloid leukemia breast cancer breast carcinoma cancer celiac disease cerebral degeneration clubfoot coloboma congenital disorder of glycosylation Id congenital disorder of glycosylation If congenital disorder of glycosylation type I congenital disorder of glycosylation developmental and epileptic encephalopathy 36 diarrhea embryoma epilepsy esophagus squamous cell carcinoma head and neck squamous cell carcinoma hypertropia laryngeal squamous cell carcinoma mechanical strabismus microcephaly nonsyndromic congenital nail disorder 9 obsolete infantile epileptic encephalopathy ophthalmoplegia optic atrophy strabismus visual epilepsy
10715	ceramide synthase 1	CERS1 Aliases: LAG1 UOG1	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Unverricht-Lundborg syndrome arteriosclerotic cardiovascular disease atherosclerosis blepharospasm cancer central nervous system cancer congestive heart failure coronary artery disease dementia dengue disease dentatorubral-pallidoluysian atrophy double outlet right ventricle early myoclonic encephalopathy embryoma focal hand dystonia gliosarcoma hand, foot and mouth disease head and neck squamous cell carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability learning disability malaria mixed glioma multiple types of congenital heart defects 6 neuroblastoma papillary adenocarcinoma papillary renal cell carcinoma primary spontaneous pneumothorax progressive myoclonus epilepsy 4 progressive myoclonus epilepsy 8 progressive myoclonus epilepsy steatotic liver disease tetralogy of Fallot thyroid gland papillary carcinoma ulcerative colitis viral infectious disease visceral heterotaxy visual epilepsy yellow fever
253430	inositol polyphosphate multikinase	IPMK	Homo sapiens (human)	Alzheimer's disease Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease cancer hepatitis idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease ovarian cancer ovarian carcinoma parapsoriasis psoriasis pustulosis of palm and sole ulcerative colitis
18	4-aminobutyrate aminotransferase	ABAT Aliases: 4-aminobutyrate transaminase GABA transaminase GABA-T GABAT gamma-aminobutyrate aminotransferase	Homo sapiens (human)	Alzheimer's disease GABA aminotransferase deficiency Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lennox-Gastaut syndrome Parkinsonism Pick's disease West syndrome alcohol dependence alcohol use disorder amnestic disorder anxiety disorder arthritis arthropathy autism spectrum disorder autistic disorder cancer cocaine abuse cocaine dependence depressive disorder dissociative amnesia embryoma epilepsy esophagitis essential hypertension essential thrombocythemia focal epilepsy gastroesophageal reflux disease hematologic cancer heroin dependence hypertension ischemia leukodystrophy major depressive disorder mood disorder morphine dependence myelodysplastic syndrome neurotic disorder obsolete infantile epileptic encephalopathy opiate dependence osteoarthritis partial motor epilepsy peptic esophagitis phobic disorder recurrent hypersomnia reflex epilepsy secondary Parkinson disease status epilepticus substance abuse substance-related disorder visual epilepsy
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
6513	solute carrier family 2 member 1	SLC2A1	Homo sapiens (human)	Alzheimer's disease Hirschsprung's disease carbohydrate metabolic disorder childhood absence epilepsy childhood onset GLUT1 deficiency syndrome 2 diabetes mellitus dystonia 9 hemangioma hypertension hypothyroidism idiopathic generalized epilepsy 12 middle cerebral artery infarction myelomeningocele nephroblastoma obesity pre-eclampsia type 2 diabetes mellitus
246	arachidonate 15-lipoxygenase	ALOX15 Aliases: 15-LOX-1	Homo sapiens (human)	Alzheimer's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Rett syndrome acute leukemia acute myocardial infarction adult lymphoma allergic asthma allergic bronchopulmonary aspergillosis amyloidosis amyotrophic lateral sclerosis anxiety disorder arthritis arthropathy asthma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma brain ischemia breast ductal carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cholangiocarcinoma chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congestive heart failure coronary artery disease coronary thrombosis dental caries dentin caries dermatitis distal arthrogryposis embryoma eosinophilic esophagitis epilepsy esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis gastroenteritis generalized anxiety disorder glomerulonephritis ileitis ileocolitis intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor kidney disease large intestine cancer leukostasis lung cancer lung carcinoma malignant mesothelioma multiple sclerosis myocardial infarction nephritis neuropathy nodular prostate osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma parapsoriasis peripheral nervous system disease progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma psoriasis pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma silent myocardial infarction stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tuberculosis urinary bladder cancer
3952	leptin	LEP	Homo sapiens (human)	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acute pancreatitis adult respiratory distress syndrome alcohol dependence alcoholic liver cirrhosis asthma breast cancer chronic obstructive pulmonary disease congenital leptin deficiency cystic fibrosis end stage renal disease familial hyperlipidemia gestational diabetes glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma hyperinsulinism hypertension hypogonadism lipid metabolism disorder lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoarthritis osteoporosis pre-eclampsia primary biliary cholangitis renal cell carcinoma rhinitis short bowel syndrome steatotic liver disease type 2 diabetes mellitus
10891	PPARG coactivator 1 alpha	PPARGC1A	Homo sapiens (human)	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome age related macular degeneration amblyopia amyotrophic lateral sclerosis cardiovascular system disease chronic obstructive pulmonary disease colitis congenital hypothyroidism diabetic retinopathy dilated cardiomyopathy heart disease hyperglycemia hyperthyroidism kidney cancer kidney failure macular degeneration malignant fibrous histiocytoma melanoma metabolic dysfunction-associated steatotic liver disease myocardial infarction nephrotic syndrome obesity placental insufficiency prediabetes syndrome primary biliary cholangitis renal fibrosis sciatic neuropathy steatotic liver disease type 2 diabetes mellitus
5335	phospholipase C gamma 1	PLCG1 Aliases: NCKAP3 PLC-II PLC148 PLCgamma1	Homo sapiens (human)	Alzheimer's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kaposi's sarcoma Meckel syndrome Miller-Dieker lissencephaly syndrome Richter's syndrome SADDAN Sezary's disease T-cell acute lymphoblastic leukemia X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 abdominal obesity-metabolic syndrome 1 achondroplasia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma allergic asthma angioedema angioimmunoblastic T-cell lymphoma angiosarcoma arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrial fibrillation autosomal dominant polycystic kidney disease bacterial sepsis bipolar disorder bone osteosarcoma borderline personality disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer cerebral infarction cerebrovascular disease childhood angiosarcoma childhood osteosarcoma chromosome 17p13.1 deletion syndrome chronic lymphocytic leukemia colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cribriform carcinoma depressive disorder diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia familial adenomatous polyposis focal segmental glomerulosclerosis fragile X syndrome gastric adenocarcinoma gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma glycoproteinosis granular cell carcinoma hepatocellular carcinoma high grade glioma hypertension ileitis ileocolitis immune system disease impulse control disorder intermittent explosive disorder intrinsic asthma irritant dermatitis kleptomania large intestine cancer laryngeal squamous cell carcinoma leukemia lissencephaly liver angiosarcoma liver cancer luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder maturity-onset diabetes of the young melancholic depression mixed glioma mucolipidosis II alpha/beta myelodysplastic syndrome obsolete melancholia oral candidiasis oral squamous cell carcinoma osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma placental insufficiency primary cutaneous T-cell non-Hodgkin lymphoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia squamous cell carcinoma steatotic liver disease tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urticaria visual epilepsy
3481	insulin like growth factor 2	IGF2	Homo sapiens (human)	Alzheimer's disease Lewy body dementia Parkinson's disease Silver-Russell syndrome acquired immunodeficiency syndrome alcohol use disorder alcoholic neuropathy brain infarction breast cancer choriocarcinoma congenital diaphragmatic hernia congenital disorder of glycosylation Ia gastrointestinal system disease hepatocellular carcinoma inflammatory bowel disease liver cirrhosis meningitis multiple sclerosis multiple system atrophy osteoarthritis osteoporosis rheumatoid arthritis type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ventricular septal defect
5333	phospholipase C delta 1	PLCD1 Aliases: 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 Phospholipase C δ1	Homo sapiens (human)	Alzheimer's disease Marfan syndrome actinic keratosis alopecia amyotrophic lateral sclerosis arthritis arthropathy blepharitis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma chronic myeloid leukemia colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary artery vasospasm cystic fibrosis diabetes mellitus embryoma esophagus squamous cell carcinoma essential hypertension glycoproteinosis hypertension impulse control disorder intermittent explosive disorder irritant dermatitis kleptomania large intestine cancer lung benign neoplasm lung cancer lung carcinoma microphthalmia mucolipidosis II alpha/beta nephrolithiasis nonsyndromic congenital nail disorder 3 obsolete Matthew-Wood syndrome obsolete asthenopia osteoarthritis parapsoriasis progressive muscular atrophy psoriasis pustulosis of palm and sole sarcomatoid carcinoma seborrheic keratosis situs inversus skin disease squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus uric acid nephrolithiasis
2932	glycogen synthase kinase 3 beta	GSK3B	Homo sapiens (human)	Alzheimer's disease Parkinson's disease acute myocardial infarction amyotrophic lateral sclerosis bipolar disorder colon cancer colorectal adenocarcinoma degenerative disc disease depressive disorder diabetic encephalopathy endometrial carcinoma heart disease hypertension middle cerebral artery infarction myocardial infarction oral squamous cell carcinoma schizophrenia sciatic neuropathy status epilepticus substance-related disorder type 2 diabetes mellitus vascular dementia
119391	glutathione S-transferase omega 2	GSTO2	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder asthma
9446	glutathione S-transferase omega 1	GSTO1	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder
1432	mitogen-activated protein kinase 14	MAPK14	Homo sapiens (human)	Alzheimer's disease Parkinson's disease anti-basement membrane glomerulonephritis colon cancer colorectal carcinoma diabetic neuropathy gastric adenocarcinoma nasopharynx carcinoma osteoporosis rectum cancer
572	BCL2 associated agonist of cell death	BAD	Homo sapiens (human)	Alzheimer's disease Parkinsonism acute kidney failure brain ischemia breast cancer colon cancer diabetic neuropathy endometrial cancer gastric ulcer glaucoma high grade glioma hypertension hypothyroidism impotence intermittent claudication lung non-small cell carcinoma macular degeneration middle cerebral artery infarction obesity osteoarthritis pancreatic cancer prostate carcinoma prostatic hypertrophy pulmonary fibrosis renal cell carcinoma traumatic brain injury type 2 diabetes mellitus visual epilepsy
5506	protein phosphatase 1 regulatory subunit 3A	PPP1R3A Aliases: GM glycogen-associated regulatory subunit of protein phosphatase-1 protein phosphatase 1 regulatory subunit GM	Homo sapiens (human)	Alzheimer's disease adult lymphoma atrial fibrillation atypical chronic myeloid leukemia, BCR-ABL1 negative breast cancer cancer carcinoma central nervous system lymphoma childhood lymphoma chronic monocytic leukemia colorectal cancer colorectal carcinoma communication disorder congestive heart failure diabetes mellitus diabetic ketoacidosis embryoma glucose intolerance hematologic cancer hypoglycemia language disorder large intestine cancer laryngeal squamous cell carcinoma lymphoid leukemia lymphoma myeloid leukemia obsolete ymphosarcoma prediabetes syndrome prostate cancer prostate carcinoma sarcomatoid carcinoma type 2 diabetes mellitus
3356	5-hydroxytryptamine receptor 2A	HTR2A	Homo sapiens (human)	Alzheimer's disease alcohol dependence alcohol use disorder alcoholic psychosis anorexia nervosa autism spectrum disorder bladder neck obstruction chronic obstructive pulmonary disease cocaine abuse cocaine dependence congenital diaphragmatic hernia congestive heart failure depressive disorder hyperglycemia hypertension inflammatory and toxic neuropathy major depressive disorder nicotine dependence non-alcoholic fatty liver obesity obsessive-compulsive disorder pancreatitis pathological gambling schizophrenia steatotic liver disease withdrawal disorder
5465	peroxisome proliferator activated receptor alpha	PPARA	Homo sapiens (human)	Alzheimer's disease alcoholic hepatitis coronary artery disease cystic fibrosis hepatocellular carcinoma hydrocephalus hypertension hypertensive encephalopathy lipid metabolism disorder myocardial infarction obesity periodontitis schizophrenia steatotic liver disease
8660	insulin receptor substrate 2	IRS2	Homo sapiens (human)	Alzheimer's disease amnestic disorder glucose metabolism disease intellectual disability metabolic dysfunction-associated steatotic liver disease osteoporosis type 2 diabetes mellitus
3572	interleukin 6 cytokine family signal transducer	IL6ST	Homo sapiens (human)	Alzheimer's disease arteriosclerosis brain ischemia hepatocellular carcinoma hyper IgE recurrent infection syndrome 4 hyperandrogenism hypertension primary immunodeficiency disease rheumatoid arthritis status epilepticus stomach cancer visual epilepsy

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