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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 "glycosyltransferase activity"

Displaying entries **51 - 75** of **140293** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
4249	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	MGAT5 Aliases: GNT-V MGAT5A alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A	Homo sapiens (human)	Henoch-Schoenlein purpura Richter's syndrome Zollinger-Ellison syndrome adenocarcinoma adenoma bile duct adenocarcinoma bile duct cancer bile duct carcinoma breast cancer breast carcinoma cancer carcinoma central nervous system cancer cholangiocarcinoma chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colonic benign neoplasm depressive disorder diabetic ketoacidosis embryoma follicular adenoma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma hyperinsulinism hypersensitivity vasculitis inflammatory bowel disease 1 inflammatory bowel disease invasive ductal carcinoma liver cancer lung benign neoplasm melanoma microcystic adenoma mixed glioma multiple sclerosis neuroblastoma nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 papillary adenoma papillary renal cell carcinoma parapsoriasis prostate cancer prostate carcinoma proteinuria psoriasis pustulosis of palm and sole renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma stomach cancer stomach carcinoma systemic lupus erythematosus 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 urinary bladder cancer
4507	methylthioadenosine phosphorylase	MTAP Aliases: MSAP S-methyl-5'-thioadenosine phosphorylase c86fus	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Ehlers-Danlos syndrome Ewing sarcoma Langerhans-cell histiocytosis Q fever Sezary's disease T-cell acute lymphoblastic leukemia X-linked ichthyosis acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult fibrosarcoma adult lymphoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis benign deep fibrous histiocytoma benign mesothelioma benign pleural mesothelioma biliary tract benign neoplasm biliary tract cancer bone cancer bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral infarction cerebrovascular disease childhood T-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia childhood lymphoma childhood osteosarcoma chondrosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer common bile duct neoplasm coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma diaphyseal medullary stenosis with malignant fibrous histiocytoma diffuse large B-cell lymphoma dysplastic nevus syndrome embryoma endometrial cancer endometrial carcinoma epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma familial retinoblastoma fibrosarcoma follicular adenoma gallbladder disease gastric adenocarcinoma gastrointestinal stromal tumor giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma hidradenoma high grade glioma histiocytoma laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoma malignant mesothelioma malignant pleural mesothelioma mantle cell lymphoma melanoma microcystic adenoma mixed glioma mycosis fungoides myeloid leukemia myocardial infarction nasopharynx carcinoma neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurofibromatosis nodular malignant melanoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma oropharynx cancer osteogenesis imperfecta osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma papillary renal cell carcinoma periampullary adenocarcinoma peripheral T-cell lymphoma pleurisy primary cutaneous T-cell non-Hodgkin lymphoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulohistiocytic granuloma reticulosarcoma retinoblastoma sarcoma sarcomatoid carcinoma sarcomatoid mesothelioma sarcomatoid renal cell carcinoma sclerosing hemangioma sensorineural hearing loss silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag sleeping sickness spindle cell sarcoma squamous cell carcinoma stomach cancer stomach carcinoma syringoma tongue squamous cell carcinoma trilateral retinoblastoma trypanosomiasis tubular adenocarcinoma typhus uterine corpus cancer vestibular schwannomatosis
4860	purine nucleoside phosphorylase	PNP Aliases: PUNP	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 Chagas disease Evans' syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Lesch-Nyhan syndrome MELAS syndrome MHC class II deficiency Nezelof syndrome Omenn syndrome Pick's disease Reye syndrome Richter's syndrome T cell deficiency acute lymphoblastic leukemia adenosine deaminase deficiency adult lymphoma agammaglobulinemia agnosia alternating hemiplegia of childhood anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autonomic neuropathy bladder carcinoma breast cancer breast carcinoma cancer carcinoma carotid artery disease central nervous system disease central nervous system lymphoma central nervous system vasculitis central retinal vein occlusion cerebral degeneration cerebral malaria cerebral palsy childhood acute lymphocytic leukemia childhood lymphoma chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer combined T cell and B cell immunodeficiency coronary artery disease critical illness polyneuropathy cutaneous leishmaniasis cyclic hematopoiesis developmental coordination disorder diabetic cataract diabetic retinopathy disease of metabolism embryoma esophageal cancer esophageal carcinoma fetal erythroblastosis gangliosidosis giant cell glioblastoma glioblastoma granulomatous angiitis head and neck squamous cell carcinoma hematologic cancer hepatocellular carcinoma herpes simplex high grade glioma hyperuricemia immune system disease inflammatory and toxic neuropathy intellectual disability large intestine cancer learning disability liver cancer locked-in syndrome lupus erythematosus lymphoblastic lymphoma lymphoma lymphopenia macrocytic anemia malaria maxillary sinus squamous cell carcinoma melanoma meningoencephalitis molybdenum cofactor deficiency type A monoclonal gammopathy of uncertain significance nervous system disease neuroblastoma neurodegenerative disease neuropathy obsolete T lymphocyte deficiency obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma periodontal disease periodontitis peripheral T-cell lymphoma peripheral nervous system disease phosphoribosylpyrophosphate synthetase superactivity pneumonia polyneuropathy primary immunodeficiency disease prostate cancer prostate carcinoma purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder quadriplegia reflex sympathetic dystrophy retinal vein occlusion sarcomatoid carcinoma severe combined immunodeficiency sinusitis skin melanoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy substance abuse substance-related disorder systemic lupus erythematosus thyroid gland medullary carcinoma trypanosomiasis tuberculosis urinary bladder cancer urinary tract obstruction vascular disease
5277	phosphatidylinositol glycan anchor biosynthesis class A	PIGA Aliases: GPI3 GPI3 (SPT14) homolog (S. cerevisiae) PIG-A Phosphatidylinositol N-acetylglucosaminyltransferase subunit A paroxysmal nocturnal hemoglobinuria	Homo sapiens (human)	Barrett's esophagus Burkitt lymphoma Hirschsprung's disease Marfan syndrome Miller-Dieker lissencephaly syndrome Simpson-Golabi-Behmel syndrome type 1 Simpson-Golabi-Behmel syndrome type 2 Unverricht-Lundborg syndrome West syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency aplastic anemia 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 atypical hemolytic-uremic syndrome autoimmune disease autoimmune lymphoproliferative syndrome autosomal recessive congenital ichthyosis 4B blepharospasm blood coagulation disease bone marrow cancer brain disease cancer chondroma chromosome 17p13.1 deletion syndrome coronary thrombosis dental caries dentin caries developmental and epileptic encephalopathy 3 early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy esophagitis esophagus adenocarcinoma essential thrombocythemia extramedullary plasmacytoma fetal erythroblastosis focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth hematopoietic system disease hemoglobinuria hemolytic anemia hemolytic-uremic syndrome immune system disease inflammatory bowel disease intellectual disability learning disability lissencephaly multiple congenital anomalies-hypotonia-seizures syndrome 2 multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm myocardial infarction obsolete congenital ichthyosiform erythroderma obsolete infantile epileptic encephalopathy paroxysmal nocturnal hemoglobinuria patent foramen ovale peptic esophagitis plasma cell neoplasm plasmacytoma polycythemia vera primary pulmonary hypertension protein C deficiency protein S deficiency pulmonary embolism sensorineural hearing loss silent myocardial infarction situs inversus thrombophilia thrombotic thrombocytopenic purpura transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis vertebrobasilar insufficiency visual epilepsy
5471	phosphoribosyl pyrophosphate amidotransferase	PPAT Aliases: GPAT PRAT	Homo sapiens (human)	alcohol dependence alcohol use disorder breast cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatoblastoma hepatocellular carcinoma liver cancer ovarian cancer ovarian carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma
5716	proteasome 26S subunit, non-ATPase 10	PSMD10	Homo sapiens (human)	B-cell lymphoma T-cell acute lymphoblastic leukemia West Nile fever acute myocardial infarction adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult cystic teratoma adult teratoma autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma brain cancer breast cancer breast carcinoma cancer carcinoma central nervous system cancer childhood osteosarcoma childhood testicular germ cell tumor cholangiocarcinoma cholesteatoma of middle ear cholesteatoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary thrombosis cystic teratoma dedifferentiated liposarcoma diabetes mellitus diabetic ketoacidosis distal arthrogryposis ehrlichiosis embryoma embryonal cancer embryonal carcinoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometriosis of ovary endometriosis of uterus endometriosis epilepsy esophageal cancer esophageal carcinoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial adenomatous polyposis 1 familial adenomatous polyposis familial retinoblastoma follicular adenoma gastroenteritis germ cell and embryonal cancer germ cell cancer germinoma gliosarcoma head and neck squamous cell carcinoma hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma high grade glioma ileitis ileocolitis immune system disease inflammatory bowel disease influenza intrahepatic cholangiocarcinoma invasive ductal carcinoma islet cell tumor large intestine cancer liposarcoma liver cancer liver carcinoma liver cirrhosis lung cancer lung non-small cell carcinoma malignant teratoma mature teratoma melanoma microcystic adenoma mixed glioma multiple myeloma multiple sclerosis myelitis myocardial infarction myopia nonpapillary renal cell carcinoma normal pressure hydrocephalus obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma pleomorphic liposarcoma polyp of middle ear prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma retinoblastoma retinopathy of prematurity sarcomatoid renal cell carcinoma schizophrenia seminoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma teratoma testicular cancer testicular germ cell cancer testicular malignant germ cell cancer testis seminoma thymic carcinoma thymoma tongue squamous cell carcinoma trilateral retinoblastoma type 2 diabetes mellitus uterine corpus cancer viral infectious disease visual epilepsy
5834	glycogen phosphorylase B	PYGB Aliases: glycogen phosphorylase, brain form	Homo sapiens (human)	acute myocardial infarction adenoid cystic carcinoma breast cancer cancer coronary artery disease coronary thrombosis diabetes mellitus embryoma lung cancer lung non-small cell carcinoma myocardial infarction salivary gland adenoid cystic carcinoma salivary gland cancer silent myocardial infarction type 2 diabetes mellitus
5836	glycogen phosphorylase L	PYGL Aliases: GSD6 Hers disease glycogen phosphorylase, liver form glycogen storage disease type VI	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia cystinuria galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IV glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease hepatocellular carcinoma hypoglycemia lactic acidosis liver cancer
5837	glycogen phosphorylase, muscle associated	PYGM Aliases: GSD5 McArdle syndrome glycogen phosphorylase, muscle form glycogen storage disease type V myophosphorylase	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Peutz-Jeghers syndrome X-linked myopathy with excessive autophagy 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 bacterial sepsis breast cancer breast carcinoma cancer carcinoma cholestasis coronary artery disease cystinuria disease of metabolism distal myopathy facioscapulohumeral muscular dystrophy familial adenomatous polyposis familial periodic paralysis galactosemia gastrinoma glucosephosphate dehydrogenase deficiency glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease gout head and neck squamous cell carcinoma insulinoma invasive lobular carcinoma islet cell tumor isolated elevated serum creatine phosphokinase levels kidney failure limb-girdle muscular dystrophy lipoma melanoma multiple endocrine neoplasia type 1 multiple symmetric lipomatosis muscular dystrophy myoglobinuria 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 oculopharyngeal muscular dystrophy pleomorphic lipoma pre-eclampsia pseudosarcomatous fibromatosis sarcomatoid carcinoma skin melanoma vitelliform macular dystrophy von Hippel-Lindau disease
5986	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	RFNG	Homo sapiens (human)
6184	ribophorin I	RPN1 Aliases: OST1 oligosaccharyltransferase 1 homolog (S. cerevisiae) oligosaccharyltransferase complex subunit (non-catalytic)	Homo sapiens (human)	Burkitt lymphoma acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis childhood leukemia chronic kidney disease coronary artery disease leukemia nutmeg liver
6185	ribophorin II	RPN2 Aliases: RIBIIR RPN-II RPNII SWP1 oligosaccharyltransferase complex subunit (non-catalytic)	Homo sapiens (human)	bipolar disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer colon carcinoma colorectal cancer colorectal carcinoma diabetes mellitus embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nasopharynx carcinoma prostate cancer prostate carcinoma schizoaffective disorder schizophrenia schizophreniform disorder stomach cancer stomach carcinoma type 2 diabetes mellitus
6480	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	ST6GAL1 Aliases: CDw75 ST6Gal I	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 Graves' disease IgA glomerulonephritis Kawasaki disease Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia adenocarcinoma adenoma adult hepatocellular carcinoma alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis allergic asthma allergic contact dermatitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bladder carcinoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma childhood hepatocellular carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma diabetes mellitus diabetic ketoacidosis embryoma esophageal cancer esophageal carcinoma gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatitis hepatocellular carcinoma high grade glioma hyperthyroidism influenza intrinsic asthma large intestine cancer liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microphthalmia mixed glioma obesity obsolete Matthew-Wood syndrome ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma parapsoriasis primary immunodeficiency disease prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole rheumatoid arthritis sarcomatoid carcinoma scleroderma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma systemic scleroderma thyrotoxicosis tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer
6482	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	ST3GAL1 Aliases: CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase SIATFL ST3Gal I ST3GalA.1 ST3O	Homo sapiens (human)	Graves' disease bipolar disorder bladder carcinoma breast cancer breast carcinoma cancer cervical squamous cell carcinoma chronic myeloid leukemia embryoma hyperthyroidism mucopolysaccharidosis IV mucopolysaccharidosis IVA ovarian cancer ovarian carcinoma ovary serous adenocarcinoma prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder scleroderma skin squamous cell carcinoma systemic scleroderma thyrotoxicosis urinary bladder cancer
6483	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	ST3GAL2 Aliases: ST3GALII ST3GalA.2	Homo sapiens (human)	Parkinson's disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma late onset Parkinson's disease mucopolysaccharidosis IV mucopolysaccharidosis IVA nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
6484	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	ST3GAL4 Aliases: FLJ11867 SAT3 ST3Gal IV STZ	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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenoid cystic carcinoma alopecia amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant intellectual developmental disorder 4 autosomal dominant intellectual developmental disorder 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 brain stem infarction campomelic dysplasia cancer carcinoma cardiomyopathy cataract cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma chromophobe renal cell carcinoma chronic fatigue syndrome clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis craniometaphyseal dysplasia dementia depressive disorder diabetes mellitus diabetic autonomic neuropathy diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy diabetic retinopathy dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal myopathy dysthymic disorder embryoma encephalitis encephalomyelitis endomyocardial fibrosis essential hypertension facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy familial hyperlipidemia frontotemporal dementia gallbladder disease gestational diabetes granuloma annulare hepatocellular carcinoma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypoglycemia large intestine cancer limb-girdle muscular dystrophy liver cancer liver disease major depressive disorder melancholic depression melanoma mucopolysaccharidosis IV mucopolysaccharidosis IVA muscular dystrophy myelitis myocardial infarction neuropathy neurotic disorder nonpapillary renal cell carcinoma 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 obsolete type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoporosis pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis retrograde amnesia salivary gland adenoid cystic carcinoma salivary gland cancer sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma steatotic liver disease thrombophilia tongue squamous cell carcinoma 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
6487	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	ST3GAL3 Aliases: N-acetyllactosaminide alpha-2,3-sialyltransferase ST3Gal III	Homo sapiens (human)	Unverricht-Lundborg syndrome West syndrome agnosia amyotrophic lateral sclerosis attention deficit hyperactivity disorder autosomal recessive intellectual developmental disorder 12 autosomal recessive intellectual developmental disorder bipolar disorder blepharospasm brain cancer breast cancer breast carcinoma cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma choreatic disease congenital disorder of glycosylation depressive disorder developmental and epileptic encephalopathy 15 developmental coordination disorder diabetes mellitus dysthymic disorder dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy embryoma epilepsy focal epilepsy focal hand dystonia hepatocellular carcinoma influenza intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer major depressive disorder melancholic depression microcephaly neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia pancreatic adenocarcinoma partial motor epilepsy progressive muscular atrophy prostate cancer prostate carcinoma pterygium schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
6489	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1	ST8SIA1 Aliases: ST8Sia I	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma cancer central nervous system cancer cerebral degeneration chronic myeloid leukemia colorectal cancer colorectal carcinoma coronary artery disease endocrine exophthalmos gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma high grade glioma invasive ductal carcinoma large intestine cancer liver disease lung benign neoplasm lung carcinoma melanoma mixed glioma multiple sclerosis neuroblastoma primary immunodeficiency disease secondary Parkinson disease skin melanoma thromboangiitis obliterans toxic encephalopathy
7357	UDP-glucose ceramide glucosyltransferase	UGCG Aliases: GCS ceramide glucosyltransferase glucosylceramide synthase	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 Fabry disease Gaucher's disease type I Gaucher's disease Niemann-Pick disease type C1 Niemann-Pick disease Pick's disease Reye syndrome Sandhoff disease acute myeloid leukemia aggressive NK-cell leukemia amyotrophic lateral sclerosis anemia brain stem infarction breast adenocarcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cerebral artery occlusion cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood leukemia chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus corneal disease coronary artery disease cystic kidney disease dementia depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma double outlet right ventricle dysthymic disorder embryoma epilepsy essential hypertension giant cell glioblastoma glioblastoma glycine encephalopathy head and neck cancer head and neck squamous cell carcinoma hematologic cancer hemolytic anemia hepatocellular carcinoma high grade glioma hydrocephalus hyperglycemia hypertension intellectual disability invasive ductal carcinoma keratoconus kidney disease learning disability leukemia lipid storage disease liver cancer lung cancer lung non-small cell carcinoma macrocytic anemia major depressive disorder medulloblastoma medulloepithelioma melancholic depression multiple myeloma myelomeningocele narcolepsy neuroectodermal tumor neurotic disorder non-congenital cyst of kidney obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete melancholia obstructive hydrocephalus ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary renal cell carcinoma pharyngitis pneumonia post-traumatic stress disorder progressive muscular atrophy psoriatic arthritis rheumatoid arthritis senile degeneration of brain sick sinus syndrome status epilepticus steatotic liver disease stomach cancer stomach carcinoma subacute delirium supratentorial primitive neuroectodermal tumor tethered spinal cord syndrome thyroid gland papillary carcinoma type 2 diabetes mellitus visual epilepsy
7363	UDP glucuronosyltransferase family 2 member B4	UGT2B4 Aliases: UGT2B11	Homo sapiens (human)	breast cancer cancer cerebral infarction cerebrovascular disease cholestasis embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma hepatocellular carcinoma liver cancer primary biliary cholangitis steatotic liver disease
7364	UDP glucuronosyltransferase family 2 member B7	UGT2B7 Aliases: UGT2B9	Homo sapiens (human)	agnosia bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardia cancer cardiovascular system disease clear cell renal cell carcinoma colorectal cancer colorectal carcinoma congestive heart failure diarrhea embryoma endometrial cancer endometrial carcinoma epilepsy gallbladder disease heart disease hepatitis hepatocellular carcinoma kidney cancer large intestine cancer leukopenia liver cancer liver carcinoma liver disease renal carcinoma renal cell carcinoma sarcomatoid carcinoma sickle cell anemia transitional cell carcinoma tuberculosis urinary bladder cancer uterine corpus cancer visual epilepsy
7365	UDP glucuronosyltransferase family 2 member B10	UGT2B10	Homo sapiens (human)	cancer embryoma prostate cancer prostate carcinoma
7366	UDP glucuronosyltransferase family 2 member B15	UGT2B15 Aliases: UGT2B8	Homo sapiens (human)	anxiety disorder breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma diabetes mellitus epilepsy generalized anxiety disorder hepatocellular carcinoma hyperandrogenism large intestine cancer liver cancer nodular prostate phobic disorder prostate adenocarcinoma prostate cancer prostate carcinoma prostatic adenoma stomach cancer stomach carcinoma type 2 diabetes mellitus
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
7368	UDP glycosyltransferase 8	UGT8 Aliases: 2-hydroxyacylsphingosine 1-beta-galactosyltransferase	Homo sapiens (human)	Barrett's esophagus GM2 gangliosidosis adenocarcinoma adenoma adult oligodendroglioma adult respiratory distress syndrome allergic rhinitis anthracosilicosis anthracosis asbestosis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer childhood oligodendroglioma classic galactosemia congenital hemolytic anemia cribriform carcinoma cystinuria dilated cardiomyopathy 1A dilated cardiomyopathy embryoma epilepsy esophagus adenocarcinoma favism galactokinase deficiency galactosemia gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma hepatocellular carcinoma hereditary elliptocytosis high grade glioma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma mixed glioma mixed oligodendroglioma-astrocytoma myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 newborn respiratory distress syndrome oligodendroglioma pancreatic cancer pancreatic carcinoma parapsoriasis parietal foramina prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole skin melanoma split hand-foot malformation 1 split hand-foot malformation 2 split hand-foot malformation 3 split hand-foot malformation 4 split hand-foot malformation 5 split hand-foot malformation 6 split hand-foot malformation tubular adenocarcinoma vasomotor rhinitis visual epilepsy

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