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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	October 29, 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 **7401 - 7425** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
41	acid sensing ion channel subunit 1	ASIC1	Homo sapiens (human)
390928	acid phosphatase 7, tartrate resistant (putative)	ACP7 Aliases: FLJ16165 PAPL PAPL1 purple acid phosphatase long form 1	Homo sapiens (human)
54	acid phosphatase 5, tartrate resistant	ACP5 Aliases: HPAP TRAP TRAcP human purple acid phosphatase tartrate-resistant acid phosphatase	Homo sapiens (human)
93650	acid phosphatase 4	ACP4 Aliases: testicular acid phosphatase	Homo sapiens (human)
55	acid phosphatase 3	ACP3 Aliases: ACP-3 PAP TM-PAP prostatic acid phosphatase	Homo sapiens (human)
53	acid phosphatase 2, lysosomal	ACP2 Aliases: LAP lysosomal acid phosphatase	Homo sapiens (human)
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
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
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
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
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
39	acetyl-CoA acetyltransferase 2	ACAT2 Aliases: Acetyl-CoA acetyltransferase, cytosolic acetoacetyl Coenzyme A thiolase	Homo sapiens (human)	amyotrophic lateral sclerosis androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis beta-ketothiolase deficiency breast cancer cholecystolithiasis choledocholithiasis cholelithiasis choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease hepatitis C hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease liver cancer nutmeg liver papillary renal cell carcinoma premature menopause progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma syndromic X-linked intellectual disability type 10 ulcerative colitis
38	acetyl-CoA acetyltransferase 1	ACAT1 Aliases: THIL acetoacetyl Coenzyme A thiolase	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 Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Crohn's colitis Crohn's disease Pick's disease Reye syndrome adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland hyperfunction adrenocortical carcinoma adult hepatocellular carcinoma age related macular degeneration agnosia alopecia amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ataxia telangiectasia atherosclerosis bacterial sepsis beta-ketothiolase deficiency bronchus cancer bronchus carcinoma cancer carbohydrate metabolic disorder cardiovascular system disease central nervous system cancer cerebral degeneration chancroid childhood hepatocellular carcinoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cribriform carcinoma cystathioninuria degeneration of macula and posterior pole developmental coordination disorder diabetes mellitus diarrhea disease of metabolism dry eye syndrome embryoma end stage renal disease epilepsy essential hypertension familial hyperlipidemia familial nephrotic syndrome focal epilepsy gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma heart disease hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hypertension hyperuricemia hypoglycemia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder intellectual disability kwashiorkor lactic acidosis large intestine cancer learning disability leptospirosis lipoid nephrosis liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lymphogranuloma venereum macular degeneration malignant teratoma marasmus mature teratoma mixed glioma necrotizing ulcerative gingivitis nephrotic syndrome neuroblastoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete Cushing's syndrome papillary renal cell carcinoma partial motor epilepsy pneumocystosis primary hyperaldosteronism prostate cancer prostate carcinoma protein-energy malnutrition rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma steatotic liver disease syndromic X-linked intellectual disability 94 teratoma thrombocytosis trypanosomiasis tubular adenocarcinoma type 2 diabetes mellitus tyrosinemia type I tyrosinemia ulcerative colitis urea cycle disorder uterine cancer uterine corpus cancer visual epilepsy xanthomatosis xerophthalmia yaws
65985	acetoacetyl-CoA synthetase	AACS Aliases: ACSF1 FLJ12389 SUR-5 acyl-CoA synthetase family member 1	Homo sapiens (human)	acute myeloid leukemia bacterial sepsis idiopathic scoliosis neuroblastoma obesity steatotic liver disease
23172	abraxas 2, BRISC complex subunit	ABRAXAS2	Homo sapiens (human)
10152	abl interactor 2	ABI2	Homo sapiens (human)
10006	abl interactor 1	ABI1	Homo sapiens (human)
11057	abhydrolase domain containing 2, acylglycerol lipase	ABHD2	Homo sapiens (human)
140701	abhydrolase domain containing 16B	ABHD16B Aliases: dJ591C20.1	Homo sapiens (human)
25864	abhydrolase domain containing 14A	ABHD14A Aliases: DKFZP564O243 DORZ1	Homo sapiens (human)
84945	abhydrolase domain containing 13	ABHD13 Aliases: BEM46L1 FLJ14906 bA153I24.2	Homo sapiens (human)
145447	abhydrolase domain containing 12B	ABHD12B Aliases: BEM46L3	Homo sapiens (human)
26090	abhydrolase domain containing 12, lysophospholipase	ABHD12 Aliases: ABHD12A BEM46L2 DKFZP434P106 dJ965G21.2	Homo sapiens (human)
55347	abhydrolase domain containing 10, depalmitoylase	ABHD10 Aliases: FLJ11342 Mycophenolic acid acyl-glucuronide esterase, mitochondrial	Homo sapiens (human)
84696	abhydrolase domain containing 1	ABHD1	Homo sapiens (human)

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