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 **201 - 225** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
3030	hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha	HADHA Aliases: GBP LCEH LCHAD MTPA gastrin-binding protein long-chain 2-enoyl-CoA hydratase long-chain-3-hydroxyacyl-CoA dehydrogenase mitochondrial trifunctional protein, alpha subunit	Homo sapiens (human)	Alzheimer's disease Barth syndrome HELLP syndrome Norum disease Reye syndrome Tangier disease X-linked dilated cardiomyopathy abetalipoproteinemia acquired immunodeficiency syndrome adult respiratory distress syndrome agnosia alpha 1-antitrypsin deficiency alternating exotropia amyotrophic lateral sclerosis arthritis arthropathy blindness breast cancer bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease cholestasis choreaacanthocytosis clubfoot cone-rod dystrophy congenital adrenal hyperplasia congenital stationary night blindness 1A congenital stationary night blindness congestive heart failure coronary artery disease cystinuria cytochrome-c oxidase deficiency disease developmental coordination disorder diabetes mellitus 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 metabolism endomyocardial fibrosis epilepsy exotropia familial hypertrophic cardiomyopathy familial periodic paralysis fibromyalgia fundus albipunctatus galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hemophagocytic lymphohistiocytosis hepatitis C human immunodeficiency virus infectious disease hypercalcemia hypertrophic cardiomyopathy hypoglycemia hypolipoproteinemia hypoparathyroidism inflammatory bowel disease inherited metabolic disorder intellectual disability lactic acidosis learning disability lipid metabolism disorder liver disease lung benign neoplasm lung cancer lung carcinoma metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency mitral valve insufficiency mitral valve prolapse monocular exotropia myoglobinuria myopathy myopia myositis nephrocalcinosis neuropathy newborn respiratory distress syndrome night blindness obesity obsolete asthenopia osteoarthritis peripheral nervous system disease phosphorus metabolism disease placental insufficiency polyneuropathy pre-eclampsia progressive muscular atrophy prostate cancer prostate carcinoma prostatitis pseudohypoparathyroidism pseudosarcomatous fibromatosis retinal disease retinitis pigmentosa retinitis sick sinus syndrome staphyloma posticum steatotic liver disease sudden infant death syndrome tricuspid valve insufficiency type 2 diabetes mellitus urea cycle disorder visual epilepsy von Willebrand's disease 2 von Willebrand's disease
10720	UDP glucuronosyltransferase family 2 member B11	UGT2B11	Homo sapiens (human)	cholangiocarcinoma intrahepatic cholangiocarcinoma prostate cancer prostate carcinoma
348158	acyl-CoA synthetase medium chain family member 2B	ACSM2B Aliases: HXMA HYST1046 xenobiotic/medium chain fatty acid:CoA ligase	Homo sapiens (human)
6470	serine hydroxymethyltransferase 1	SHMT1 Aliases: 14 kDa protein MGC15229 MGC24556 SHMT cSHMT cytoplasmic serine hydroxymethyltransferase	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Down syndrome Langerhans-cell histiocytosis Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia alcohol use disorder alopecia alternating hemiplegia of childhood autistic disorder autonomic neuropathy bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system disease central nervous system lymphoma cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital heart disease cribriform carcinoma embryoma epilepsy esophagus squamous cell carcinoma essential hypertension follicular adenoma gastric cardia adenocarcinoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatocellular carcinoma hyperhomocysteinemia hyperphosphatemia hypertension intestinal benign neoplasm intestinal cancer large intestine cancer laryngeal benign neoplasm laryngeal disease larynx cancer leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma microcystic adenoma multiple sclerosis nephroblastoma nervous system disease non-Hodgkin lymphoma obsolete ymphosarcoma optic papillitis ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma papilledema prostate cancer prostate carcinoma reticulosarcoma retinal edema sarcomatoid carcinoma schizophrenia situs inversus squamous cell carcinoma temporal arteritis thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal disease tuberous sclerosis tubular adenocarcinoma urinary bladder cancer
1604	CD55 molecule (Cromer blood group)	CD55 Aliases: CR CROM TC	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Barrett's esophagus Budd-Chiari syndrome IgA glomerulonephritis Kallmann syndrome Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Pick's disease Plasmodium vivax malaria Reye syndrome Richter's syndrome Sheehan syndrome T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome Werner syndrome acoustic neuroma acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome agammaglobulinemia age related macular degeneration amphetamine abuse amyloidosis anaplastic astrocytoma anemia angiomatous meningioma aplastic anemia arthritis arthropathy atopic dermatitis atrial fibrillation autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome bacterial infectious disease benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma bullous pemphigoid cancer carcinoma central nervous system lymphoma cerebral convexity meningioma cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood lymphoma cholangiocarcinoma cholera chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia chronic pyelonephritis clear cell meningioma colitis colon cancer 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 congenital hemolytic anemia cribriform carcinoma critical illness polyneuropathy deficiency anemia degeneration of macula and posterior pole dermatitis diabetes mellitus diabetic ketoacidosis diarrhea embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma endometriosis of ovary endometriosis of uterus endometriosis esophagus adenocarcinoma essential thrombocythemia eunuchism familial adenomatous polyposis 1 familial adenomatous polyposis favism fetal erythroblastosis fibrillary astrocytoma fibrous meningioma follicular lymphoma gastroenteritis gastrointestinal stromal tumor gemistocytic astrocytoma granular cell carcinoma hemoglobinopathy hemolytic anemia hepatitis C hereditary elliptocytosis hereditary spherocytosis high grade glioma hypochromic anemia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis ileus immune system disease inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal obstruction intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency juvenile pilocytic astrocytoma kwashiorkor large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lymphoma macrocytic anemia macroglobulinemia macular degeneration malaria malignant astrocytoma marasmus meningioma meningoencephalitis meningothelial meningioma microcystic meningioma microcytic anemia myasthenia gravis myelodysplastic syndrome myositis neuroblastoma neuromyelitis optica neuropathy non-Hodgkin lymphoma nutrition disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma olfactory groove meningioma ovarian cancer ovarian carcinoma panhypopituitarism parasagittal meningioma paroxysmal nocturnal hemoglobinuria peripheral nervous system disease pilocytic astrocytoma pituitary adenoma pneumonia polyneuropathy progeria prostate cancer prostate carcinoma protein-energy malnutrition protein-losing enteropathy proteinuria protoplasmic astrocytoma psammomatous meningioma pulmonary embolism pure red-cell aplasia recurrent hypersomnia reticulosarcoma rheumatoid arthritis sarcoidosis sarcomatoid carcinoma secondary hypertrophic osteoarthropathy secretory meningioma septooptic dysplasia sickle cell anemia skin squamous cell carcinoma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic primary carnitine deficiency disease thalassemia thrombosis thrombotic thrombocytopenic purpura transitional meningioma tropical sprue tuberculosis tubular adenocarcinoma type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis uterine corpus cancer
81793	toll like receptor 10	TLR10	Homo sapiens (human)	asthma
4099	myelin associated glycoprotein	MAG	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 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 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 type 5 Charcot-Marie-Tooth disease Guillain-Barre syndrome Kearns-Sayre syndrome Lewy body dementia MASA syndrome Marfan syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pelizaeus-Merzbacher disease Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome acute myocardial infarction adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood amyloidosis angioma serpiginosum arteriosclerotic cardiovascular disease astigmatism atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy brain stem infarction cancer capillary hemangioma cavernous hemangioma central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chorioangioma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy compartment syndrome congenital diarrhea 5 with tufting enteropathy congenital nystagmus coronary artery disease coronary thrombosis critical illness polyneuropathy demyelinating disease demyelinating polyneuropathy depressive disorder disease of mental health dissociated nystagmus dysthymic disorder embryoma familial multiple nevi flammei gliosarcoma glomus tumor hemangioma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia high grade glioma histiocytoid hemangioma hyperopia immune system disease inflammatory and toxic neuropathy intellectual disability intramuscular hemangioma learning disability lesion of sciatic nerve leukodystrophy lymphangioma major depressive disorder melancholic depression melanoma meningoencephalitis middle cerebral artery infarction mixed glioma monoclonal gammopathy of uncertain significance monoclonal paraproteinemia motor peripheral neuropathy multiple sclerosis myocardial infarction nerve compression syndrome nervous system disease neuroblastoma neuromuscular disease neuropathy neurotic disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia optic atrophy optic neuritis pancreatic cancer paraplegia pathologic nystagmus peripheral nervous system disease placental insufficiency plasma cell neoplasm poikiloderma with neutropenia polyneuropathy polyradiculoneuropathy prostate cancer prostate carcinoma psychotic disorder schizophrenia sciatic neuropathy secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma spontaneous ocular nystagmus substance abuse substance-related disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis
8605	phospholipase A2 group IVC	PLA2G4C Aliases: cPLA2-gamma	Homo sapiens (human)	adult oligodendroglioma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis autism spectrum disorder autistic disorder breast cancer cancer central nervous system cancer childhood oligodendroglioma chronic obstructive pulmonary disease gliosarcoma hepatitis C high grade glioma intrinsic asthma mixed glioma mixed oligodendroglioma-astrocytoma oligodendroglioma schizophrenia
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
57171	dolichyldiphosphatase 1	DOLPP1 Aliases: LSFR2 linked to Surfeit genes in Fugu rubripes 2	Homo sapiens (human)	endometrial cancer endometrial carcinoma uterine corpus cancer
2530	fucosyltransferase 8	FUT8 Aliases: alpha (1,6) fucosyltransferase	Homo sapiens (human)	Laron syndrome achondroplasia adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma buphthalmos cancer chronic fatigue syndrome chronic myeloid leukemia chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congenital disorder of glycosylation coronary artery disease embryoma encephalitis encephalomyelitis epilepsy follicular adenoma glaucoma hepatitis A hepatitis C hepatitis hepatocellular carcinoma hydrophthalmos idiopathic interstitial pneumonia intellectual disability juvenile glaucoma large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma microcephaly microcystic adenoma myelitis ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm papillary adenoma papillary carcinoma placental insufficiency polyhydramnios postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pseudomyxoma peritonei pulmonary emphysema pulmonary fibrosis schizophrenia scoliosis skin melanoma visual epilepsy
1551	cytochrome P450 family 3 subfamily A member 7	CYP3A7 Aliases: CP37 P450-HFLA	Homo sapiens (human)	adult respiratory distress syndrome allergic asthma asthma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma embryoma endometrial cancer endometrial carcinoma hepatocellular carcinoma intrinsic asthma liver cancer liver cirrhosis lung cancer lung carcinoma newborn respiratory distress syndrome sarcomatoid carcinoma seminoma testicular cancer testicular malignant germ cell cancer testis seminoma uterine corpus cancer
159371	solute carrier family 35 member G1	SLC35G1 Aliases: C10orf60 FLJ33990 POST partner of STIM1	Homo sapiens (human)	Laron syndrome Werner syndrome acute myeloid leukemia agnosia arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis atrial fibrillation autistic disorder breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma coronary artery disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma epilepsy hemolytic-uremic syndrome hepatoblastoma hepatocellular carcinoma hyperglycemia intussusception kidney failure large intestine cancer leukemia major depressive disorder melancholic depression mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neurotic disorder nutmeg liver obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 occipital horn syndrome polycystic ovary syndrome progeria prostate cancer prostate carcinoma schizophrenia sensorineural hearing loss transient myeloproliferative 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 uremia
5167	ectonucleotide pyrophosphatase/phosphodiesterase 1	ENPP1 Aliases: PC-1 PCA1	Homo sapiens (human)	Ehlers-Danlos syndrome HCL-V Laron syndrome McCune Albright syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired hyperkeratosis acute myocardial infarction adult astrocytic tumor allergic asthma amelogenesis imperfecta anaplastic astrocytoma anemia angioid streaks ankylosing spondylitis ankylosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arterial calcification of infancy arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autosomal dominant hypophosphatemic rickets autosomal recessive hypophosphatemic rickets autosomal recessive osteopetrosis 7 bicuspid aortic valve disease bile duct adenocarcinoma bile duct cancer bile duct carcinoma bile duct disease blindness bone disease brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cardiovascular system disease carotid artery disease cartilage disease cerebral infarction cerebrovascular disease childhood astrocytic tumor childhood cerebral astrocytoma cholangiocarcinoma chondrocalcinosis chronic kidney disease colorectal cancer colorectal carcinoma congenital hypothyroidism congenital toxoplasmosis congestive heart failure connective tissue disease coronary artery disease coronary thrombosis craniosynostosis diabetes mellitus diabetic ketoacidosis embryoma encephalitis encephalomyelitis end stage renal disease endometriosis of ovary endometriosis of uterus endometriosis enthesopathy essential hypertension exanthem fibrillary astrocytoma gemistocytic astrocytoma gestational diabetes giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance hairy cell leukemia heart disease hepatitis C hepatocellular carcinoma hereditary elliptocytosis herpes simplex high grade glioma hypercalcemia hypercementosis hyperglycemia hyperinsulinism hyperphosphatemic familial tumoral calcinosis hypertension hypophosphatemia hypothyroidism insulinoma intermittent claudication intrinsic asthma juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure large intestine cancer linear nevus sebaceous syndrome liver cancer lung benign neoplasm lung cancer lung carcinoma macrocytic anemia malignant astrocytoma melanoma mitral valve insufficiency mitral valve prolapse mongolian spot monoclonal gammopathy of uncertain significance morbid obesity mucopolysaccharidosis IV multiple epiphyseal dysplasia multiple myeloma musculoskeletal system disease myelitis myocardial infarction myopia myxedema nephritis nephrocalcinosis nephrosis neurogenic arthropathy nodular prostate nonepidermolytic palmoplantar keratoderma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 ossification of the posterior longitudinal ligament of spine osteoarthritis osteochondrodysplasia osteogenesis imperfecta osteomalacia osteopetrosis osteoporosis osteosclerosis otitis media palmoplantar keratosis pancreatic cancer pancreatic carcinoma periarthritis perinatal intestinal perforation peripheral artery disease peripheral vascular disease phosphorus metabolism disease pilocytic astrocytoma plasmacytoma pneumocystosis polycystic ovary syndrome polycythemia vera polycythemia postural orthostatic tachycardia syndrome pre-eclampsia prediabetes syndrome prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma pseudoxanthoma elasticum pulmonary valve stenosis pyoureter restrictive cardiomyopathy retinal disease retinitis rheumatoid arthritis rickets sarcomatoid carcinoma scoliosis sensorineural hearing loss silent myocardial infarction skin melanoma spondyloarthropathy spondylosis steatotic liver disease subependymal giant cell astrocytoma suppurative periapical periodontitis tendinitis tropical sprue 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 uremia viral infectious disease
8987	starch binding domain 1	STBD1 Aliases: FLJ41801 GENX-3414 genethonin 1	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease glycogen storage disease II
8708	beta-1,3-galactosyltransferase 1	B3GALT1 Aliases: beta3Gal-T1	Homo sapiens (human)	Peters plus syndrome adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
26007	triokinase and FMN cyclase	TKFC Aliases: DKFZP586B1621 FAD-AMP lyase (cyclizing) NET45	Homo sapiens (human)	cataract diabetes mellitus diabetic ketoacidosis liver disease type 2 diabetes mellitus
346689	killer cell lectin like receptor G2	KLRG2 Aliases: C-type lectin domain family 15, member B CLEC15B FLJ44186	Homo sapiens (human)	prostate cancer prostate carcinoma
116285	acyl-CoA synthetase medium chain family member 1	ACSM1 Aliases: MACS1	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 carcinoma cerebral palsy depressive disorder essential hypertension hemiplegia hypertension idiopathic scoliosis lung benign neoplasm lung carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia sarcomatoid carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
138050	heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT Aliases: FLJ32731 HGNAT	Homo sapiens (human)	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
2194	fatty acid synthase	FASN Aliases: 3-hydroxyacyl-[acyl-carrier-protein] dehydratase 3-oxoacyl-[acyl-carrier-protein] reductase 3-oxoacyl-[acyl-carrier-protein] synthase Acyl-[acyl-carrier-protein] hydrolase Enoyl-[acyl-carrier-protein] reductase FAS SDR27X1 [Acyl-carrier-protein] S-acetyltransferase [Acyl-carrier-protein] S-malonyltransferase short chain dehydrogenase/reductase family 27X, member 1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Barrett's esophagus Japanese encephalitis Marinesco-Sjogren syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome X-linked dilated cardiomyopathy Zollinger-Ellison syndrome acoustic neuroma acute chest syndrome adenocarcinoma adenoma adrenal gland hyperfunction adult liposarcoma adult oligodendroglioma agnosia angiomatous meningioma arrhythmogenic right ventricular cardiomyopathy arthritis arthropathy autoimmune lymphoproliferative syndrome bacterial sepsis basal cell carcinoma benign breast phyllodes tumor benign meningioma bladder carcinoma blindness bone cancer bone osteosarcoma brain cancer breast cancer breast carcinoma breast malignant phyllodes tumor bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cerebral convexity meningioma cerebral degeneration chikungunya childhood liposarcoma childhood oligodendroglioma childhood osteosarcoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia clear cell meningioma clear cell renal cell carcinoma clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital hypothyroidism congestive heart failure cribriform carcinoma dedifferentiated liposarcoma dengue disease dengue hemorrhagic fever depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma 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 metabolism dysplastic nevus syndrome embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epithelioid leiomyosarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial retinoblastoma fibrous meningioma fundus albipunctatus gastric adenocarcinoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma granular cell tumor head and neck cancer hepatitis B hepatitis C hepatocellular carcinoma herpes simplex high grade glioma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypothyroidism idiopathic interstitial pneumonia inflammatory bowel disease 1 inflammatory bowel disease inflammatory liposarcoma intellectual disability intraorbital meningioma intraventricular meningioma kidney cancer large intestine cancer learning disability leiomyoma leiomyosarcoma leukemia leukopenia liposarcoma liver cancer liver carcinoma luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma mantle cell lymphoma melanoma meningioma meningothelial meningioma metabolic dysfunction-associated steatotic liver disease microcystic meningioma microinvasive gastric cancer microphthalmia mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma muscular disease myelitis myofibroma myotonic dystrophy type 1 myotonic dystrophy type 2 myxedema myxoid leiomyosarcoma nasopharynx carcinoma neurofibromatosis obesity obsolete Cushing's syndrome obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ocular cancer olfactory groove meningioma oligodendroglioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma pleomorphic adenoma carcinoma pleomorphic adenoma pleomorphic liposarcoma polycystic kidney disease 3 postinflammatory pulmonary fibrosis primary cerebellar degeneration primary hyperaldosteronism primary immunodeficiency disease prostate adenocarcinoma prostate cancer prostate carcinoma psammomatous meningioma pulmonary fibrosis renal carcinoma renal cell carcinoma renal osteodystrophy retinitis pigmentosa retinoblastoma rippling muscle disease 2 sarcomatoid carcinoma sclerosing liposarcoma sebaceous carcinoma secretory meningioma skin melanoma speech-language disorder-1 spinal meningioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma sweat gland cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma transitional meningioma trilateral retinoblastoma tuberculosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer uterine fibroid varicocele vestibular schwannomatosis viral infectious disease well-differentiated liposarcoma yellow fever
55915	LanC like glutathione S-transferase 2	LANCL2	Homo sapiens (human)
7358	UDP-glucose 6-dehydrogenase	UGDH Aliases: GDH UDP-GlcDH UDPGDH UGD uridine-diphospho glucose dehydrogenase	Homo sapiens (human)	Graves' disease Laron syndrome Zollinger-Ellison syndrome achondroplasia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cholangiocarcinoma developmental and epileptic encephalopathy 84 diarrhea enophthalmos giant cell glioblastoma giardiasis glioblastoma hepatocellular carcinoma high grade glioma hyperinsulinism hyperthyroidism hypoglycemia intrahepatic cholangiocarcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma obsolete exophthalmos orbital disease peripheral artery disease placental insufficiency primary hyperoxaluria thalassemia thyrotoxicosis
7021	transcription factor AP-2 beta	TFAP2B	Homo sapiens (human)	Char syndrome angle-closure glaucoma patent ductus arteriosus sleep disorder
222	aldehyde dehydrogenase 3 family member B2	ALDH3B2	Homo sapiens (human)	Sjogren-Larsson syndrome alcohol dependence alcohol use disorder

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