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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

Search results for "glucuronosyltransferase activity"

Displaying entries **1 - 25** of **5715** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
54490	UDP glucuronosyltransferase family 2 member B28	UGT2B28	Homo sapiens (human)	Addison's disease adrenal cortical hypofunction cancer colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer primary cutaneous amyloidosis prostate cancer prostate carcinoma
27087	beta-1,3-glucuronyltransferase 1	B3GAT1 Aliases: GlcAT-P HNK-1 NK-1 galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 glucuronosyltransferase P	Homo sapiens (human)	Alport syndrome 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 Down syndrome Ewing sarcoma Felty's syndrome Goodpasture 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 Lown-Ganong-Levine syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Takayasu's arteritis Wolff-Parkinson-White syndrome Zika fever acoustic neuroma acquired hyperkeratosis acquired immunodeficiency syndrome actinic keratosis acute lymphoblastic leukemia adult acute lymphocytic leukemia aggressive NK-cell leukemia agnosia agranulocytosis allergic asthma anaplastic astrocytoma anxiety disorder arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome axonal neuropathy bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cartilage disease cataract 5 multiple types celiac disease cellular schwannoma cerebral cavernous malformation 1 cerebral degeneration cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chromophobe renal cell carcinoma chronic NK-cell lymphocytosis chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma complex regional pain syndrome congenital myasthenic syndrome connective tissue disease coronary artery disease critical illness polyneuropathy depressive disorder diabetic ketoacidosis disease of mental health dysthymic disorder embryoma encephalomyelitis epidermolysis bullosa epithelioid sarcoma esophageal cancer esophageal carcinoma essential hypertension exostosis fibrillary astrocytoma fibrous dysplasia gastroparesis gemistocytic astrocytoma generalized anxiety disorder gestational diabetes giant cell glioblastoma glioblastoma glycine encephalopathy granulomatosis with polyangiitis hairy cell leukemia hemophagocytic lymphohistiocytosis hepatitis C hepatitis D high grade glioma human immunodeficiency virus infectious disease hypersensitivity vasculitis hypertension idiopathic interstitial pneumonia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inflammatory breast carcinoma influenza intrinsic asthma juvenile pilocytic astrocytoma keratoacanthoma large intestine cancer leukemia leukopenia lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphopenia major depressive disorder malaria malignant astrocytoma malignant peripheral nerve sheath tumor melancholic depression melanoma melanotic neurilemmoma meningoencephalitis metanephric adenoma mucocutaneous leishmaniasis multiple myeloma multiple sclerosis myasthenia gravis myeloid leukemia myeloproliferative disorder with eosinophilia neurilemmoma neuroblastoma neurodegenerative disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder neutropenia nonpapillary renal cell carcinoma obsolete constipation obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea osteoarthritis papillary carcinoma papillary renal cell carcinoma papilloma periapical granuloma peripheral nervous system disease phobic disorder pilocytic astrocytoma plasma cell neoplasm pleomorphic adenoma plexiform schwannoma polyarteritis nodosa polyneuropathy polyradiculoneuropathy post-traumatic stress disorder postinflammatory pulmonary fibrosis primary biliary cholangitis primary sclerosing cholangitis prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder pulmonary fibrosis renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder sclerosing cholangitis severe congenital neutropenia skin melanoma speech-language disorder-1 spindle cell sarcoma squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer subependymal giant cell astrocytoma sudden infant death syndrome tongue squamous cell carcinoma tuberculosis 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 ulcerative colitis uveal melanoma viral infectious disease
54658	UDP glucuronosyltransferase family 1 member A1	UGT1A1 Aliases: UGT1A	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 Carney complex Crigler-Najjar syndrome Crohn's colitis Crohn's disease Fabry disease Gaucher's disease Gilbert syndrome Graves' disease 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 Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute kidney failure acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute pyelonephritis adenocarcinoma adenoma adult respiratory distress syndrome agranulocytosis allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia amnestic disorder anemia arteriosclerotic cardiovascular disease asthma atherosclerosis autism spectrum disorder autistic disorder bacterial sepsis beta thalassemia biliary tract cancer bilirubin metabolic disorder bladder carcinoma brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease cervical squamous cell carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chromophobe renal cell carcinoma chronic myeloid leukemia chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diarrhea 6 congenital hemolytic anemia congestive heart failure contact dermatitis coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis cystinuria denture stomatitis diabetes mellitus diabetic ketoacidosis diarrhea differentiated thyroid gland carcinoma duodenum cancer embryoma endometrial cancer endometrial carcinoma epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension female reproductive organ cancer follicular adenoma galactosemia gallbladder disease gastrointestinal system cancer glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematopoietic system disease hemiplegia hemochromatosis type 1 hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobin H disease hemoglobinopathy hemolytic anemia hepatitis A hepatitis B hepatitis C hepatitis D hepatitis hepatocellular carcinoma hereditary spherocytosis human immunodeficiency virus infectious disease hyperinsulinism hypertension hyperthyroidism hypertrophic pyloric stenosis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kernicterus due to isoimmunization kernicterus kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer leukopenia lipid storage disease liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoblastic lymphoma macrocytic anemia microcystic adenoma myeloid leukemia myocardial infarction neonatal jaundice nephrolithiasis neutropenia newborn respiratory distress syndrome nodular prostate nonpapillary renal cell carcinoma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 occupational dermatitis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma peripheral artery disease prostate cancer prostate carcinoma prostatic adenoma rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retrograde amnesia sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seminoma sensorineural hearing loss severe congenital neutropenia sickle cell anemia silent myocardial infarction small intestine adenocarcinoma small intestine cancer small intestine carcinoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma stomatitis testicular cancer testis seminoma thalassemia thrombocytopenia thyrotoxicosis tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ulcerative stomatitis uric acid nephrolithiasis urinary bladder cancer uterine corpus cancer visual epilepsy xeroderma pigmentosum group D
2131	exostosin glycosyltransferase 1	EXT1 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase ttv	Homo sapiens (human)	Alzheimer's disease Cenani-Lenz syndactyly syndrome Cornelia de Lange syndrome 4 Cornelia de Lange syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Legg-Calve-Perthes disease Lennox-Gastaut syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Ollier disease Pick's disease Reye syndrome Ritter's disease Werner syndrome achondroplasia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia anaplastic astrocytoma antisocial personality disorder arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chondroblastoma chondroma chondrosarcoma cleidocranial dysplasia clubfoot conduct disorder connective tissue disease cranial nerve disease cranial nerve palsy cribriform carcinoma cryoglobulinemia diabetes mellitus disease of mental health embryoma endometrial cancer endometrial carcinoma epilepsy exostosis familial hypercholesterolemia familial nephrotic syndrome fibrillary astrocytoma fibromyalgia frontotemporal dementia gallbladder disease gemistocytic astrocytoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydrocephalus hyperostosis hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease intellectual disability juvenile myoclonic epilepsy juvenile pilocytic astrocytoma learning disability leukemia lipoid nephrosis liver cancer liver disease lupus nephritis malignant astrocytoma membranous glomerulonephritis metachondromatosis microcephaly mixed glioma mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple myeloma myositis nephrotic syndrome osteoarthritis osteonecrosis osteopoikilosis osteoporosis osteosarcoma periarthritis personality disorder pilocytic astrocytoma progeria protoplasmic astrocytoma psychotic disorder radioulnar synostosis rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis schizophrenia scoliosis spinal cord disease subependymal giant cell astrocytoma tendinitis thrombophilia trichorhinophalangeal syndrome type II tubular adenocarcinoma type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer vasculitis vesicoureteral reflux visual epilepsy
2132	exostosin glycosyltransferase 2	EXT2 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase SOTV	Homo sapiens (human)	Alzheimer's disease Cenani-Lenz syndactyly syndrome Dent disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Marfan syndrome Ollier disease Pick's disease Reye syndrome achondroplasia adenosarcoma agnosia anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease cerebral degeneration cherubism chondrosarcoma cleidocranial dysplasia clubfoot congenital hypothyroidism congenital nystagmus connective tissue disease cranial nerve disease cranial nerve palsy craniosynostosis cryptorchidism developmental and epileptic encephalopathy 36 developmental coordination disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus epilepsy esophagitis essential hypertension exostosis familial hypercholesterolemia frontotemporal dementia gastroesophageal reflux disease hereditary multiple exostoses humeroradial synostosis hyperostosis hypertension hypertropia hypothyroidism immune system disease intellectual disability large intestine cancer learning disability lupus nephritis macrocytic anemia mechanical strabismus membranous glomerulonephritis metachondromatosis microcephaly mucopolysaccharidosis III mucopolysaccharidosis type IIIA myxedema nephroblastoma nonsyndromic congenital nail disorder 9 obsolete constipation ophthalmoplegia osteoarthritis osteonecrosis osteosarcoma parietal foramina pathologic nystagmus peptic esophagitis periarthritis radioulnar synostosis scoliosis situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus tendinitis tuberous sclerosis type 2 diabetes mellitus ventricular septal defect visual epilepsy
9215	LARGE xylosyl- and glucuronyltransferase 1	LARGE1 Aliases: KIAA0609 like-acetylglucosaminyltransferase	Homo sapiens (human)	Axenfeld-Rieger syndrome Becker muscular dystrophy Bell's palsy Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome achondroplasia acoustic neuroma agnosia amphetamine abuse angiomatous meningioma atypical chronic myeloid leukemia, BCR-ABL1 negative 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 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 benign meningioma bilateral optic nerve hypoplasia blindness buphthalmos cancer cataract centronuclear myopathy cerebral convexity meningioma chronic monocytic leukemia clear cell meningioma cleft lip cleft palate coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cone-rod dystrophy 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-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A6 congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder diabetes mellitus dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial periodic paralysis fibrous meningioma fundus albipunctatus fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hydrophthalmos hypertropia idiopathic scoliosis imperforate anus intellectual disability intraorbital meningioma intraventricular meningioma isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly liver cancer lymphoid leukemia lymphoplasmacyte-rich meningioma major depressive disorder mechanical strabismus megaconial type congenital muscular dystrophy megalocornea melancholic depression meningioma meningocele meningothelial meningioma microcephaly microcystic meningioma microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myeloid leukemia myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia nemaline myopathy 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 melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy olfactory groove meningioma ophthalmoplegia optic atrophy parasagittal meningioma pathologic nystagmus peripheral retinal degeneration pituitary adenoma pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 psammomatous meningioma recurrent corneal erosion renal agenesis retinal detachment retinitis pigmentosa rhabdomyosarcoma rigid spine muscular dystrophy 1 rippling muscle disease 2 scoliosis secretory meningioma senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder spinal meningioma spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type transitional meningioma type 2 diabetes mellitus visual epilepsy
7367	UDP glucuronosyltransferase family 2 member B17	UGT2B17	Homo sapiens (human)	Barrett's esophagus Graves' disease Richter's syndrome adenocarcinoma adenoma age related macular degeneration ankylosing spondylitis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cribriform carcinoma degeneration of macula and posterior pole embryoma endometrial cancer endometrial carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma glomerulonephritis granular cell carcinoma head and neck squamous cell carcinoma hematologic cancer hyperthyroidism kidney disease kidney failure large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma macular degeneration nasopharynx carcinoma nephritis nephrosis nodular prostate osteoporosis primary cutaneous amyloidosis prostate cancer prostate carcinoma prostatic adenoma pyoureter substance abuse substance-related disorder thyrotoxicosis tubular adenocarcinoma uterine corpus cancer
174517	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase sqv-8	sqv-8	Caenorhabditis elegans	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia
251900	Glucuronyltransferase I	GlcAT-I	Drosophila melanogaster (fruit fly)	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia
135152	beta-1,3-glucuronyltransferase 2	B3GAT2 Aliases: GlcAT-S galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 glucuronosyltransferase S	Homo sapiens (human)	Barrett's esophagus schizophrenia thrombophilia
280645	beta-1,3-glucuronyltransferase 2	B3gat2	Mus musculus (house mouse)	Barrett's esophagus schizophrenia
733177	beta-1,3-glucuronyltransferase 2 S homeolog	b3gat2.S	Xenopus laevis (African clawed frog)	Barrett's esophagus schizophrenia
108716933	beta-1,3-glucuronyltransferase 2 L homeolog	b3gat2.L	Xenopus laevis (African clawed frog)	Barrett's esophagus schizophrenia
445060	beta-1,3-glucuronyltransferase 2 (glucuronosyltransferase S)	b3gat2	Danio rerio (zebrafish)	Barrett's esophagus schizophrenia
64544	beta-1,3-glucuronyltransferase 2	B3gat2	Rattus norvegicus (Norway rat)	Barrett's esophagus schizophrenia
594928	beta-1,3-glucuronyltransferase 2	b3gat2	Xenopus tropicalis (tropical clawed frog)	Barrett's esophagus schizophrenia
54577	UDP glucuronosyltransferase family 1 member A7	UGT1A7 Aliases: UGT1G	Homo sapiens (human)	Crigler-Najjar syndrome Crohn's colitis Crohn's disease Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 acute pancreatitis adult hepatocellular carcinoma agranulocytosis alcoholic pancreatitis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder bladder carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest childhood hepatocellular carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease gastrointestinal system cancer glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma hemoglobin H disease hepatitis B hepatitis C hepatitis D hepatocellular carcinoma hereditary spherocytosis inflammatory bowel disease 1 inflammatory bowel disease influenza kernicterus due to isoimmunization kernicterus large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer leukopenia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma neonatal jaundice neutropenia nodular prostate obesity pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma thalassemia tongue squamous cell carcinoma tracheal disease type 2 diabetes mellitus ulcerative colitis urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
406731	UDP glucuronosyltransferase 1 family a, b	ugt1ab	Danio rerio (zebrafish)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
100384891	UDP glucuronosyltransferase 1 family, polypeptide A7	ugt1a7	Danio rerio (zebrafish)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
100489505	UDP glucuronosyltransferase 1 family, polypeptide A1	ugt1a1	Xenopus tropicalis (tropical clawed frog)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
185500	UDP-glucuronosyltransferase	ugt-61	Caenorhabditis elegans	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer
394436	UDP glucuronosyltransferase 1 family, polypeptide A1	Ugt1a1	Mus musculus (house mouse)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome bilirubin metabolic disorder breast cancer cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer type 1 diabetes mellitus type 2 diabetes mellitus
100135191	UDP glucuronosyltransferase 1 family, polypeptide A6	ugt1a6	Xenopus tropicalis (tropical clawed frog)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome bilirubin metabolic disorder breast cancer cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer type 1 diabetes mellitus type 2 diabetes mellitus
24861	UDP glucuronosyltransferase family 1 member A1	Ugt1a1	Rattus norvegicus (Norway rat)	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome bilirubin metabolic disorder breast cancer cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer type 1 diabetes mellitus type 2 diabetes mellitus
54657	UDP glucuronosyltransferase family 1 member A4	UGT1A4 Aliases: HUG-BR2 UGT1D	Homo sapiens (human)	Crigler-Najjar syndrome Fleck corneal dystrophy Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia beta thalassemia bilirubin metabolic disorder breast cancer breast carcinoma cancer carcinoma cardiac arrest celiac disease cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hematologic cancer hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver disease neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D

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