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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 **301 - 325** of **1582** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
30	acetyl-CoA acyltransferase 1	ACAA1 Aliases: Lnc-Myd88 peroxisomal 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	B-cell lymphoma Langerhans-cell histiocytosis Zellweger syndrome allergic asthma asthma beta-ketothiolase deficiency carotid artery disease hepatocellular carcinoma intrinsic asthma liver cancer lymphoma non-Hodgkin lymphoma obsolete ymphosarcoma reticulosarcoma
10449	acetyl-CoA acyltransferase 2	ACAA2 Aliases: DSAEC mitochondrial 3-oxoacyl-Coenzyme A thiolase	Homo sapiens (human)	adult respiratory distress syndrome arthritis arthropathy beta-ketothiolase deficiency hepatocellular carcinoma liver cancer newborn respiratory distress syndrome osteoarthritis
31	acetyl-CoA carboxylase alpha	ACACA Aliases: ACACalpha ACC-alpha ACC1 ACCA ACCalpha Acac1 acetyl-CoA carboxylase 1 hACC1	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 Bloch-Sulzberger syndrome Clouston syndrome Crohn's colitis Crohn's disease Graves' disease IgA glomerulonephritis Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wernicke-Korsakoff syndrome Wilson disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoid cystic carcinoma adenoma adrenal adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adult respiratory distress syndrome agenesis of the corpus callosum with peripheral neuropathy allergic rhinitis amyotrophic lateral sclerosis type 1 ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anorexia nervosa anxiety disorder aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy ataxia telangiectasia atherosclerosis atrophic gastritis attention deficit hyperactivity disorder atypical teratoid rhabdoid tumor autism spectrum disorder autistic disorder autoimmune hepatitis benign mesothelioma bipolar disorder brain stem infarction breast adenoid cystic carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma cardiomyopathy cardiovascular system disease celiac disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia chromophobe renal cell carcinoma chronic kidney disease chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism duodenum cancer dysthymic disorder embryoma endometriosis of uterus endometriosis endomyocardial fibrosis epidermal appendage tumor esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial periodic paralysis focal segmental glomerulosclerosis follicular adenoma gallbladder disease generalized anxiety disorder gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis head and neck squamous cell carcinoma heart cancer heart disease heart valve disease hemochromatosis hepatitis B hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertension hyperthyroidism hypertrichosis hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypomelanosis of Ito inflammatory bowel disease 1 inflammatory bowel disease iron metabolism disease juvenile rheumatoid arthritis kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leprosy leukemia liver cancer liver carcinoma liver disease luminal breast carcinoma A lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder malaria malignant mesothelioma malignant pleural mesothelioma megaconial type congenital muscular dystrophy melancholic depression metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease microcystic adenoma middle cerebral artery infarction migraine mitochondrial metabolism disease mitochondrial myopathy mitral valve disease muscular disease muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myocardial infarction myopathy nemaline myopathy nephritis nephrosis neuropathy neurotic disorder newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsessive-compulsive disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma ovarian cancer ovarian carcinoma papillary adenoma papillary renal cell carcinoma paraganglioma parapsoriasis periodontitis peripheral nervous system disease peroxisome biogenesis disorder 7A pheochromocytoma phobic disorder placental insufficiency polycystic ovary syndrome polyneuropathy primary ovarian insufficiency prostate adenocarcinoma prostate cancer prostate carcinoma psoriasis psoriatic arthritis pulmonary tuberculosis pustulosis of palm and sole pyoureter renal carcinoma renal cell carcinoma reticulosarcoma rheumatoid arthritis rigid spine muscular dystrophy 1 salivary gland adenoid cystic carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia scleroderma seminoma silent myocardial infarction skin benign neoplasm skin cancer small intestine cancer steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder systemic lupus erythematosus systemic scleroderma testicular cancer testis seminoma thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland follicular carcinoma thyrotoxicosis trichuriasis tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis vasomotor rhinitis viral infectious disease visual epilepsy
32	acetyl-CoA carboxylase beta	ACACB Aliases: ACACbeta ACC-beta ACC2 ACCB ACCbeta HACC275 acetyl-CoA carboxylase 2	Homo sapiens (human)	B-cell lymphoma Clostridium difficile colitis Clouston syndrome abdominal obesity-metabolic syndrome 1 acute chest syndrome acute myocardial infarction adenoid cystic carcinoma arteriosclerotic cardiovascular disease atherosclerosis cancer carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis head and neck squamous cell carcinoma high grade glioma hypopharynx cancer kidney disease large intestine cancer major depressive disorder metabolic dysfunction-associated steatotic liver disease morbid obesity muscular disease myocardial infarction nephritis nephrosis neurotic disorder nutmeg liver obesity obsolete ymphosarcoma pancreatic ductal adenocarcinoma perinatal necrotizing enterocolitis pyoureter salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma silent myocardial infarction steatotic liver disease type 2 diabetes mellitus viral infectious disease
43	acetylcholinesterase (Yt blood group)	ACHE Aliases: Yt blood group	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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Balo concentric sclerosis Chagas disease Clostridium difficile colitis Creutzfeldt-Jakob disease Duchenne muscular dystrophy Gamstorp-Wohlfart syndrome Gerstmann-Straussler-Scheinker syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IGSF1 deficiency syndrome Japanese encephalitis Kawasaki disease Lafora disease Lambert-Eaton myasthenic syndrome Lewy body dementia Marfan syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Noonan syndrome 1 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peutz-Jeghers syndrome Pick's disease Q fever Reye syndrome Schwartz-Jampel syndrome 1 Wilson-Turner syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute stress disorder adrenoleukodystrophy adult medulloblastoma allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anterior horn cell disease anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive distal hereditary motor neuronopathy 1 autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial meningitis bacterial sepsis bipolar disorder bladder carcinoma blood platelet disease brain cancer brain disease breast cancer breast carcinoma cancer cardiac arrest cardiovascular system disease carotid artery disease cauda equina neoplasm central nervous system disease central nervous system origin vertigo centronuclear myopathy X-linked centronuclear myopathy cerebellar ataxia cerebellar disease cerebral atherosclerosis cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease chancroid childhood cerebral astrocytoma childhood disintegrative disease childhood leukemia childhood medulloblastoma chromophobe renal cell carcinoma chronic kidney disease chronic monocytic leukemia chronic myelomonocytic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma cognitive disorder collecting duct carcinoma colon cancer colonic benign neoplasm colonic pseudo-obstruction colorectal cancer colorectal carcinoma congenital hypothyroidism congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myasthenic syndrome 5 congenital myasthenic syndrome congenital myopathy 1A congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital structural myopathy congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome conversion disorder coronary artery disease coronary thrombosis cystic fibrosis dementia dengue disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism dissociative amnesia dissociative disorder distal myopathy dysthymic disorder dystonia embryoma endocrine exophthalmos endometritis enophthalmos epilepsy episodic ataxia type 1 essential thrombocythemia facioscapulohumeral muscular dystrophy familial hyperlipidemia fibrillary astrocytoma fibromyalgia focal epilepsy frontotemporal dementia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder glaucoma head and neck squamous cell carcinoma heart disease hemiplegia hepatocellular carcinoma high grade glioma hyperglycemia hypothyroidism idiopathic scoliosis immune system disease impotence inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intracranial arteriosclerosis intrinsic asthma irritable bowel syndrome juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma kidney cancer large intestine cancer laryngeal squamous cell carcinoma lateral sclerosis learning disability leptospirosis leukemia limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma liver cirrhosis liver disease lower respiratory tract disease lung benign neoplasm lung cancer lung non-small cell carcinoma lung small cell carcinoma lymphogranuloma venereum major depressive disorder malaria malignant astrocytoma medulloblastoma medullomyoblastoma megaconial type congenital muscular dystrophy melancholic depression melanoma melanotic medulloblastoma migraine morbid obesity motor neuron disease movement disease multiple epiphyseal dysplasia multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myasthenia gravis myelodysplastic syndrome myelomeningocele myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis myotonic dystrophy type 2 myxedema narcolepsy nasal cavity disease necrotizing ulcerative gingivitis nemaline myopathy nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neurofibroma neuromuscular disease neuromuscular junction disease neurotic disorder nonpapillary renal cell carcinoma normocytic anemia nutmeg liver obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete constipation obsolete exophthalmos obsolete melancholia obsolete ymphosarcoma oculopharyngeal muscular dystrophy orbital disease osteochondrodysplasia osteoporosis ovarian cancer overnutrition papillary adenocarcinoma papillary renal cell carcinoma paranasal sinus disease partial motor epilepsy perineurioma peripheral nerve sheath neoplasm peripheral nervous system neoplasm persian gulf syndrome phobic disorder pilocytic astrocytoma polydactyly premature ejaculation primary pulmonary hypertension prion disease progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma psychologic dyspareunia psychotic disorder renal carcinoma renal cell carcinoma retrograde amnesia rigid spine muscular dystrophy 1 rippling muscle disease 2 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma sleeping sickness spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spinal muscular atrophy sporadic breast cancer status epilepticus stomach cancer stomach carcinoma subacute delirium subependymal giant cell astrocytoma substance abuse substance-related disorder temporal arteritis teratocarcinoma tethered spinal cord syndrome thanatophoric dysplasia thrombocytopenia thyroid gland papillary carcinoma trypanosomiasis tuberous sclerosis type 1 diabetes mellitus type 2 diabetes mellitus typhus ulcerative colitis upper respiratory tract disease urinary bladder cancer varicose veins vascular dementia viral infectious disease visual epilepsy vitiligo von Hippel-Lindau disease yaws yellow fever
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
467	activating transcription factor 3	ATF3	Homo sapiens (human)	prostate cancer pulmonary tuberculosis
468	activating transcription factor 4	ATF4	Homo sapiens (human)	borna disease prostate carcinoma pulmonary venoocclusive disease
33	acyl-CoA dehydrogenase long chain	ACADL Aliases: ACAD4 LCAD long-chain acyl-CoA dehydrogenase	Homo sapiens (human)	Pearson syndrome atrial fibrillation cancer cardiomyopathy chronic kidney disease embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fibromyalgia hepatocellular carcinoma hypertrophic cardiomyopathy hypoglycemia liver cancer liver carcinoma myositis nuclear type mitochondrial complex I deficiency 20 steatotic liver disease urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency
34	acyl-CoA dehydrogenase medium chain	ACADM Aliases: ACAD1 MCAD MCADH medium-chain acyl-CoA dehydrogenase	Homo sapiens (human)	D-bifunctional protein deficiency Reye syndrome brain edema breast cancer breast carcinoma cancer carnitine palmitoyltransferase I deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure cystinuria diarrhea disease of metabolism distal arthrogryposis epilepsy familial periodic paralysis 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 hepatitis hydrocephalus hypoglycemia hypoglycemic coma inherited metabolic disorder isolated elevated serum creatine phosphokinase levels lactic acidosis large intestine cancer liver disease long QT syndrome medium chain acyl-CoA dehydrogenase deficiency metabolic dysfunction-associated steatotic liver disease myopathy neuroblastoma neurodegenerative disease nonpapillary renal cell carcinoma obesity papillary renal cell carcinoma perinatal necrotizing enterocolitis phenylketonuria pseudosarcomatous fibromatosis psoriatic arthritis renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma sick sinus syndrome steatotic liver disease sudden infant death syndrome systemic primary carnitine deficiency disease urea cycle disorder visual epilepsy
35	acyl-CoA dehydrogenase short chain	ACADS Aliases: ACAD3 SCAD	Homo sapiens (human)	Bell's palsy Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Stevens-Johnson syndrome X-linked Aarskog syndrome alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bipolar disorder cancer cardiomyopathy chondrodysplasia-pseudohermaphroditism syndrome chronic kidney disease congestive heart failure coronary artery disease embryoma endomyocardial fibrosis epilepsy erythema multiforme facial nerve disease facial paralysis familial periodic paralysis hepatocellular carcinoma hypertrophic cardiomyopathy liver cancer medium chain acyl-CoA dehydrogenase deficiency microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II myopathy nutmeg liver pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder scoliosis short chain acyl-CoA dehydrogenase deficiency visual epilepsy
36	acyl-CoA dehydrogenase short/branched chain	ACADSB Aliases: ACAD7 SBCAD	Homo sapiens (human)	3-methylglutaconic aciduria Smith-Lemli-Opitz syndrome agnosia alternating exotropia autistic disorder breast cancer breast carcinoma developmental coordination disorder diabetes mellitus diabetic ketoacidosis epilepsy essential hypertension exotropia familial hyperlipidemia hepatocellular carcinoma hypertension hypoglycemia liver cancer microcephaly monocular exotropia short chain acyl-CoA dehydrogenase deficiency syndromic X-linked intellectual disability type 10 visual epilepsy
37	acyl-CoA dehydrogenase very long chain	ACADVL Aliases: ACAD6 LCACD VLCAD	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 Pearson syndrome Pick's disease Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 adrenal adenoma adrenal cortex cancer alpha 1-antitrypsin deficiency atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrioventricular block cardiomyopathy 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 cerebral degeneration complement component 2 deficiency congenital adrenal hyperplasia dermatitis 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 endomyocardial fibrosis familial hypertrophic cardiomyopathy familial periodic paralysis gallbladder disease hemopericardium hypercalcemia hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels lactic acidosis liver disease macroglobulinemia metabolic dysfunction-associated steatotic liver disease mitochondrial trifunctional protein deficiency myopathy nephrocalcinosis obesity obsolete lymphoplasmacytic lymphoma patent foramen ovale pericardial effusion phosphorus metabolism disease placental insufficiency pneumonia pseudosarcomatous fibromatosis sensorineural hearing loss steatotic liver disease urea cycle disorder ventricular septal defect very long chain acyl-CoA dehydrogenase deficiency von Willebrand's disease 2 von Willebrand's disease
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

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