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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 **26 - 50** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
48	aconitase 1	ACO1 Aliases: IREBP IRP1 aconitate hydratase, cytoplasmic cytosplasmic aconitase soluble aconitase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Down syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wilson disease acquired polycythemia adrenal gland cancer age related macular degeneration anemia arthritis arthropathy bipolar disorder cancer cerebral degeneration deficiency anemia degeneration of macula and posterior pole duodenal ulcer duodenum cancer dysplastic nevus syndrome embryoma erythropoietin polycythemia essential hypertension familial erythrocytosis 2 heart cancer hemochromatosis type 1 hemochromatosis hepatocellular carcinoma hypertension hypochromic anemia iron metabolism disease leech infestation liver cancer macrocytic anemia macular degeneration melanoma metabolic dysfunction-associated steatotic liver disease microcytic anemia myiasis neuroblastoma osteoarthritis pancreatic cancer pancreatic carcinoma parapsoriasis pheochromocytoma polycythemia vera polycythemia porphyria prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole skin melanoma small intestine cancer stress polycythemia toxoplasmosis
50	aconitase 2	ACO2 Aliases: ACONM aconitate hydratase, mitochondrial mitochondrial aconitase	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Crohn's colitis Crohn's disease Foster-Kennedy syndrome Friedreich ataxia 1 Friedreich ataxia Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome X-linked nonsyndromic deafness achromatopsia acquired color blindness adult respiratory distress syndrome autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness bipolar disorder blue color blindness breast cancer breast carcinoma cancer central nervous system disease cerebral degeneration clear cell renal cell carcinoma color blindness colorectal cancer colorectal carcinoma congenital nystagmus cystic fibrosis demyelinating polyneuropathy dissociated nystagmus dominant optic atrophy plus syndrome embryoma epilepsy fumarase deficiency fundus dystrophy hepatocellular carcinoma hypertropia idiopathic interstitial pneumonia infantile cerebellar-retinal degeneration inflammatory bowel disease 1 inflammatory bowel disease insulinoma kidney cancer large intestine cancer lingual-facial-buccal dyskinesia liver cancer mechanical strabismus mitochondrial DNA depletion syndrome movement disease multiple sclerosis neurodegenerative disease newborn respiratory distress syndrome nutritional optic neuropathy obsolete autosomal recessive nonsyndromic deafness 105 ophthalmoplegia optic atrophy 1 optic atrophy 9 optic atrophy optic nerve disease pathologic nystagmus postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pulmonary fibrosis red color blindness red-green color blindness renal carcinoma renal cell carcinoma schizophrenia spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ulcerative colitis visual epilepsy visual pathway disease
730249	aconitate decarboxylase 1	ACOD1 Aliases: CAD	Homo sapiens (human)	bacterial sepsis central nervous system cancer gliosarcoma hepatitis B high grade glioma lung disease mixed glioma peripheral artery disease viral infectious disease
641371	acyl-CoA thioesterase 1	ACOT1 Aliases: ACH2 CTE-1 LACH2	Homo sapiens (human)	gastric adenocarcinoma hepatocellular carcinoma liver cancer
134526	acyl-CoA thioesterase 12	ACOT12 Aliases: Cach STARD15 StAR-related lipid transfer (START) domain containing 15 THEAL	Homo sapiens (human)	hepatocellular carcinoma leukodystrophy leukoencephalopathy with vanishing white matter liver cancer
10965	acyl-CoA thioesterase 2	ACOT2 Aliases: Mte1 ZAP128 mitochondrial acyl-CoA thioesterase 1	Homo sapiens (human)	coronary artery disease diabetes mellitus type 2 diabetes mellitus
122970	acyl-CoA thioesterase 4	ACOT4 Aliases: FLJ31235 PTE-Ib PTE2B	Homo sapiens (human)	cerebral infarction cerebrovascular disease
11332	acyl-CoA thioesterase 7	ACOT7 Aliases: ACH1 ACT BACH CTE-II LACH1 Long chain acyl-CoA thioester hydrolase MGC1126 brain acyl CoA hydrolase hBACH	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 Duchenne muscular dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium vivax malaria Reye syndrome acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation bacterial infectious disease beta thalassemia blood coagulation disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer complex partial epilepsy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health distal arthrogryposis dysentery dysthymic disorder eating disorder embryoma epilepsy esophagus squamous cell carcinoma female stress incontinence gallbladder disease gestational diabetes gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis hepatocellular carcinoma high grade glioma hypereosinophilic syndrome inclusion body myositis infertility intrinsic asthma kwashiorkor large intestine cancer leprosy liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma major depressive disorder malaria marasmus melancholic depression mixed glioma multiple sclerosis muscular dystrophy myocardial infarction neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder nonpapillary renal cell carcinoma nutrition disease obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive lung disease osteomyelitis ovarian cancer ovarian carcinoma papillary renal cell carcinoma peripheral nervous system disease peroxisome biogenesis disorder 7A pertussis polyneuropathy postpartum depression pre-eclampsia prediabetes syndrome primary open angle glaucoma primary ovarian insufficiency primary pulmonary hypertension progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma protein-energy malnutrition psychotic disorder pulmonary tuberculosis renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scleroderma sick sinus syndrome silent myocardial infarction spermatic cord torsion systemic scleroderma temporal lobe epilepsy thalassemia tuberculosis tuberculous pneumothorax 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 urethral intrinsic sphincter deficiency viral infectious disease visual epilepsy
10005	acyl-CoA thioesterase 8	ACOT8 Aliases: NAP1 Nef (lentivirus myristoylated factor) associated protein 1 PTE-2 choloyl-CoA hydrolase hACTE-III hTE	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 Thiel-Behnke corneal dystrophy acquired immunodeficiency syndrome bacterial sepsis cancer cerebral degeneration diabetes insipidus diarrhea embryoma hepatocellular carcinoma human immunodeficiency virus infectious disease hypophosphatemia liver cancer low tension glaucoma lung cancer lung non-small cell carcinoma neurohypophyseal diabetes insipidus parapsoriasis psoriasis pustulosis of palm and sole
51	acyl-CoA oxidase 1	ACOX1 Aliases: PALMCOX palmitoyl-CoA oxidase	Homo sapiens (human)	Mitchell syndrome X-linked nonsyndromic deafness abdominal obesity-metabolic syndrome 1 adult lymphoma anodontia autosomal dominant auditory neuropathy 1 autosomal dominant nonsyndromic deafness 10 autosomal dominant nonsyndromic deafness 11 autosomal dominant nonsyndromic deafness 12 autosomal dominant nonsyndromic deafness 13 autosomal dominant nonsyndromic deafness 15 autosomal dominant nonsyndromic deafness 16 autosomal dominant nonsyndromic deafness 17 autosomal dominant nonsyndromic deafness 18 autosomal dominant nonsyndromic deafness 1 autosomal dominant nonsyndromic deafness 20 autosomal dominant nonsyndromic deafness 21 autosomal dominant nonsyndromic deafness 22 autosomal dominant nonsyndromic deafness 23 autosomal dominant nonsyndromic deafness 24 autosomal dominant nonsyndromic deafness 25 autosomal dominant nonsyndromic deafness 27 autosomal dominant nonsyndromic deafness 28 autosomal dominant nonsyndromic deafness 2A autosomal dominant nonsyndromic deafness 2B autosomal dominant nonsyndromic deafness 30 autosomal dominant nonsyndromic deafness 31 autosomal dominant nonsyndromic deafness 33 autosomal dominant nonsyndromic deafness 36 autosomal dominant nonsyndromic deafness 3A autosomal dominant nonsyndromic deafness 3B autosomal dominant nonsyndromic deafness 40 autosomal dominant nonsyndromic deafness 41 autosomal dominant nonsyndromic deafness 43 autosomal dominant nonsyndromic deafness 44 autosomal dominant nonsyndromic deafness 47 autosomal dominant nonsyndromic deafness 48 autosomal dominant nonsyndromic deafness 49 autosomal dominant nonsyndromic deafness 4A autosomal dominant nonsyndromic deafness 4B autosomal dominant nonsyndromic deafness 50 autosomal dominant nonsyndromic deafness 51 autosomal dominant nonsyndromic deafness 52 autosomal dominant nonsyndromic deafness 53 autosomal dominant nonsyndromic deafness 54 autosomal dominant nonsyndromic deafness 56 autosomal dominant nonsyndromic deafness 58 autosomal dominant nonsyndromic deafness 59 autosomal dominant nonsyndromic deafness 5 autosomal dominant nonsyndromic deafness 64 autosomal dominant nonsyndromic deafness 65 autosomal dominant nonsyndromic deafness 66 autosomal dominant nonsyndromic deafness 67 autosomal dominant nonsyndromic deafness 68 autosomal dominant nonsyndromic deafness 69 autosomal dominant nonsyndromic deafness 6 autosomal dominant nonsyndromic deafness 70 autosomal dominant nonsyndromic deafness 7 autosomal dominant nonsyndromic deafness 9 autosomal dominant nonsyndromic deafness autosomal recessive nonsyndromic deafness 101 autosomal recessive nonsyndromic deafness 102 autosomal recessive nonsyndromic deafness 103 autosomal recessive nonsyndromic deafness 104 autosomal recessive nonsyndromic deafness 12 autosomal recessive nonsyndromic deafness 13 autosomal recessive nonsyndromic deafness 14 autosomal recessive nonsyndromic deafness 15 autosomal recessive nonsyndromic deafness 16 autosomal recessive nonsyndromic deafness 17 autosomal recessive nonsyndromic deafness 18A autosomal recessive nonsyndromic deafness 18B autosomal recessive nonsyndromic deafness 1A autosomal recessive nonsyndromic deafness 1B autosomal recessive nonsyndromic deafness 20 autosomal recessive nonsyndromic deafness 21 autosomal recessive nonsyndromic deafness 22 autosomal recessive nonsyndromic deafness 23 autosomal recessive nonsyndromic deafness 24 autosomal recessive nonsyndromic deafness 25 autosomal recessive nonsyndromic deafness 26 autosomal recessive nonsyndromic deafness 27 autosomal recessive nonsyndromic deafness 28 autosomal recessive nonsyndromic deafness 29 autosomal recessive nonsyndromic deafness 2 autosomal recessive nonsyndromic deafness 30 autosomal recessive nonsyndromic deafness 31 autosomal recessive nonsyndromic deafness 32 autosomal recessive nonsyndromic deafness 33 autosomal recessive nonsyndromic deafness 35 autosomal recessive nonsyndromic deafness 36 autosomal recessive nonsyndromic deafness 37 autosomal recessive nonsyndromic deafness 38 autosomal recessive nonsyndromic deafness 39 autosomal recessive nonsyndromic deafness 3 autosomal recessive nonsyndromic deafness 40 autosomal recessive nonsyndromic deafness 42 autosomal recessive nonsyndromic deafness 44 autosomal recessive nonsyndromic deafness 45 autosomal recessive nonsyndromic deafness 46 autosomal recessive nonsyndromic deafness 47 autosomal recessive nonsyndromic deafness 48 autosomal recessive nonsyndromic deafness 49 autosomal recessive nonsyndromic deafness 4 autosomal recessive nonsyndromic deafness 51 autosomal recessive nonsyndromic deafness 53 autosomal recessive nonsyndromic deafness 55 autosomal recessive nonsyndromic deafness 59 autosomal recessive nonsyndromic deafness 5 autosomal recessive nonsyndromic deafness 61 autosomal recessive nonsyndromic deafness 62 autosomal recessive nonsyndromic deafness 63 autosomal recessive nonsyndromic deafness 65 autosomal recessive nonsyndromic deafness 66 autosomal recessive nonsyndromic deafness 67 autosomal recessive nonsyndromic deafness 68 autosomal recessive nonsyndromic deafness 6 autosomal recessive nonsyndromic deafness 70 autosomal recessive nonsyndromic deafness 71 autosomal recessive nonsyndromic deafness 74 autosomal recessive nonsyndromic deafness 76 autosomal recessive nonsyndromic deafness 77 autosomal recessive nonsyndromic deafness 79 autosomal recessive nonsyndromic deafness 7 autosomal recessive nonsyndromic deafness 83 autosomal recessive nonsyndromic deafness 84A autosomal recessive nonsyndromic deafness 84B autosomal recessive nonsyndromic deafness 85 autosomal recessive nonsyndromic deafness 86 autosomal recessive nonsyndromic deafness 88 autosomal recessive nonsyndromic deafness 89 autosomal recessive nonsyndromic deafness 8 autosomal recessive nonsyndromic deafness 91 autosomal recessive nonsyndromic deafness 93 autosomal recessive nonsyndromic deafness 96 autosomal recessive nonsyndromic deafness 97 autosomal recessive nonsyndromic deafness 98 autosomal recessive nonsyndromic deafness 9 autosomal recessive nonsyndromic deafness cancer central nervous system lymphoma cerebral infarction cerebrovascular disease childhood lymphoma citrullinemia colorectal cancer colorectal carcinoma cone-rod dystrophy congenital nystagmus craniosynostosis depressive disorder disease of metabolism dissociated nystagmus dysthymic disorder dystonia epilepsy familial hyperlipidemia fundus albipunctatus hepatocellular carcinoma hypertropia large intestine cancer leukodystrophy liver cancer liver carcinoma lymphoma major depressive disorder mechanical strabismus melancholic depression mitochondrial metabolism disease mitochondrial myopathy myopia neurodegenerative disease neurotic disorder obesity obsolete autosomal recessive nonsyndromic deafness 105 obsolete melancholia obsolete ymphosarcoma ophthalmoplegia optic atrophy pathologic nystagmus peroxisomal acyl-CoA oxidase deficiency peroxisomal disease retinitis pigmentosa sensorineural hearing loss speech disorder spontaneous ocular nystagmus steatotic liver disease strabismus syndromic X-linked intellectual disability 94 tooth agenesis visual epilepsy
8309	acyl-CoA oxidase 2	ACOX2 Aliases: 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanoyl-CoA 24-hydroxylase BRCACOX BRCOX THCCox branched chain acyl-CoA oxidase trihydroxycoprostanoyl-CoA oxidase	Homo sapiens (human)	Zellweger syndrome breast cancer breast carcinoma cardiovascular system disease congenital bile acid synthesis defect 6 heart disease hepatoblastoma hepatocellular carcinoma liver cancer obsolete steatorrhea peroxisome biogenesis disorder 1A
8310	acyl-CoA oxidase 3, pristanoyl	ACOX3	Homo sapiens (human)	prostate cancer prostate carcinoma
23205	acyl-CoA synthetase bubblegum family member 1	ACSBG1 Aliases: BG1 BGM FLJ30320 KIAA0631 MGC14352 bubblegum hBG1 hsBG lipidosin very long-chain acyl-CoA synthetase	Homo sapiens (human)	B-cell lymphoma Clostridium difficile colitis Crohn's colitis Crohn's disease Evans' syndrome HCL-V 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 Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome adrenoleukodystrophy autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer central nervous system lymphoma chronic kidney disease chronic lymphocytic leukemia colitis colon carcinoma colorectal cancer diffuse large B-cell lymphoma embryoma gastroenteritis gliosarcoma hairy cell leukemia hemophagocytic lymphohistiocytosis hepatocellular carcinoma high grade glioma ileitis ileocolitis ileus immune system disease inflammatory bowel disease 1 inflammatory bowel disease intestinal obstruction irritable bowel syndrome kwashiorkor late onset Parkinson's disease liver cancer long QT syndrome lung benign neoplasm lung cancer lung carcinoma lymphoma lymphoplasmacytic lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macroglobulinemia marasmus mixed glioma multiple myeloma mycosis fungoides neurocirculatory asthenia neurodegenerative disease non-Hodgkin lymphoma nutrition disease obsolete lymphoplasmacytic lymphoma obsolete ymphosarcoma primary immunodeficiency disease protein-energy malnutrition reticulosarcoma rheumatoid arthritis scleroderma systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma ulcerative colitis viral infectious disease
81616	acyl-CoA synthetase bubblegum family member 2	ACSBG2 Aliases: BGR DKFZp434K1635 PRTD-NY3 bubblegum related protein	Homo sapiens (human)	adrenoleukodystrophy male infertility tuberculosis
197322	acyl-CoA synthetase family member 3	ACSF3 Aliases: malonyl-CoA synthetase	Homo sapiens (human)	B-cell lymphoma adult lymphoma amnestic disorder brain disease central nervous system lymphoma childhood lymphoma combined malonic and methylmalonic acidemia diarrhea disease of metabolism dystonia hypoglycemia inherited metabolic disorder lymphoma methylmalonic acidemia microcephaly migraine obsolete ymphosarcoma retrograde amnesia
2180	acyl-CoA synthetase long chain family member 1	ACSL1 Aliases: ACS1 FACL1 LACS LACS1 LACS2 lignoceroyl-CoA synthase long-chain fatty-acid-coenzyme A ligase 1	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bacterial sepsis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cervix uteri carcinoma in situ chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy endomyocardial fibrosis gliosarcoma glomerulonephritis glucose metabolism disease hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease kidney disease large intestine cancer liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma mixed glioma myocardial infarction nephritis nephrosis nonpapillary renal cell carcinoma obesity obsolete type 1 diabetes mellitus 9 papillary renal cell carcinoma pyoureter renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction steatotic liver disease 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 vascular disease
2181	acyl-CoA synthetase long chain family member 3	ACSL3 Aliases: ACS3 PRO2194	Homo sapiens (human)	Sjogren-Larsson syndrome allergic asthma asthma breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer craniosynostosis embryoma familial hyperlipidemia gliosarcoma hepatitis C hepatocellular carcinoma high grade glioma intrinsic asthma liver cancer lung benign neoplasm lung cancer lung carcinoma melanoma mixed glioma non-syndromic X-linked intellectual disability 63 non-syndromic X-linked intellectual disability ovarian cancer ovarian carcinoma prostate cancer prostate carcinoma sarcoma skin melanoma syndactyly
2182	acyl-CoA synthetase long chain family member 4	ACSL4 Aliases: ACS4 LACS4 lignoceroyl-CoA synthase long-chain fatty-acid-Coenzyme A ligase 4	Homo sapiens (human)	Alport syndrome Bell's palsy Duchenne muscular dystrophy Meckel's diverticulum Sjogren-Larsson syndrome abdominal obesity-metabolic syndrome 1 adenocarcinoma adenoma anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder bacterial sepsis bipolar disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer clubfoot colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hemolytic anemia cribriform carcinoma depressive disorder disease of mental health dysthymic disorder embryoma epithelioid leiomyosarcoma epithelioid sarcoma facial nerve disease facial paralysis favism follicular adenoma generalized anxiety disorder gliosarcoma glomerulonephritis granular cell carcinoma granuloma annulare hepatocellular carcinoma hereditary elliptocytosis high grade glioma hypertropia intellectual disability kidney failure large intestine cancer learning disability leiomyosarcoma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma major depressive disorder mechanical strabismus melancholic depression microcystic adenoma mixed glioma muscular dystrophy myopia myxoid leiomyosarcoma nephritis neuromuscular disease neurotic disorder non-syndromic X-linked intellectual disability 63 non-syndromic X-linked intellectual disability obesity obsolete melancholia ophthalmoplegia osteoarthritis papillary adenoma patent ductus arteriosus placental insufficiency prostate cancer prostate carcinoma proteinuria psychotic disorder pyloric stenosis sarcoma schizophrenia sensorineural hearing loss spindle cell sarcoma steatotic liver disease stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 systemic lupus erythematosus tubular adenocarcinoma visual epilepsy
51703	acyl-CoA synthetase long chain family member 5	ACSL5 Aliases: ACS2 ACS5 FACL5 for fatty acid coenzyme A ligase 5 fatty-acid-Coenzyme A ligase, long-chain 5 long-chain acyl-CoA synthetase 5 long-chain fatty acid coenzyme A ligase 5	Homo sapiens (human)	acute chest syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma anaplastic astrocytoma basal cell carcinoma breast cancer breast carcinoma cancer carcinoma celiac disease central nervous system cancer childhood cerebral astrocytoma colorectal cancer colorectal carcinoma congenital diarrhea congestive heart failure coronary thrombosis cribriform carcinoma embryoma endometrial carcinoma essential thrombocythemia familial hyperlipidemia fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer high grade glioma juvenile pilocytic astrocytoma large intestine cancer lung benign neoplasm lung carcinoma malignant astrocytoma migraine mixed glioma myelodysplastic syndrome myocardial infarction obesity pilocytic astrocytoma protoplasmic astrocytoma sarcomatoid carcinoma sebaceous carcinoma silent myocardial infarction steatotic liver disease subependymal giant cell astrocytoma sweat gland cancer systemic lupus erythematosus tubular adenocarcinoma
23305	acyl-CoA synthetase long chain family member 6	ACSL6 Aliases: ACS2 KIAA0837 LACS2 LACS5	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 acute chest syndrome acute myeloid leukemia acute myocardial infarction amphetamine abuse androgen insensitivity syndrome arthritis arthropathy cancer cerebral degeneration congestive heart failure coronary thrombosis disease of mental health essential thrombocythemia hematologic cancer leukemia male infertility myelodysplastic syndrome myocardial infarction osteoarthritis plasmacytoma polycythemia vera polycythemia premature menopause primary ovarian insufficiency psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder silent myocardial infarction
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
123876	acyl-CoA synthetase medium chain family member 2A	ACSM2A Aliases: A-923A4.1 MGC150530	Homo sapiens (human)	cerebral palsy hemiplegia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
348158	acyl-CoA synthetase medium chain family member 2B	ACSM2B Aliases: HXMA HYST1046 xenobiotic/medium chain fatty acid:CoA ligase	Homo sapiens (human)
6296	acyl-CoA synthetase medium chain family member 3	ACSM3 Aliases: SA	Homo sapiens (human)	IgA glomerulonephritis Kallmann syndrome Marfan syndrome Sheehan syndrome abdominal obesity-metabolic syndrome 1 anemia autism spectrum disorder autistic disorder bacterial sepsis brain cancer brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease cataract cerebral artery occlusion cerebral infarction cerebrovascular disease chronic kidney disease communicating hydrocephalus diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia generalized atherosclerosis heart disease hemosiderosis hepatocellular carcinoma hereditary coproporphyria hydrocephalus hyperglycemia hypertension 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 scoliosis intracranial aneurysm intracranial vasospasm 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 liver cancer liver carcinoma macrocytic anemia obesity obstructive hydrocephalus ocular hypertension oculomotor nerve paralysis panhypopituitarism partial third-nerve palsy post-traumatic stress disorder prostate cancer prostate carcinoma senile degeneration of brain sensorineural hearing loss situs inversus tetralogy of Fallot thrombophilia thymus gland disease total third-nerve palsy transient cerebral ischemia tuberous sclerosis ulcerative colitis visual epilepsy
341392	acyl-CoA synthetase medium chain family member 4	ACSM4 Aliases: similar to olfactory specific medium-chain acyl CoA synthetase	Homo sapiens (human)

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