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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **251 - 275** of **1582** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
54575	UDP glucuronosyltransferase family 1 member A10	UGT1A10 Aliases: UGT1J	Homo sapiens (human)	Crigler-Najjar syndrome 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 bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholangiocarcinoma 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 hemoglobin H disease hepatitis D hepatocellular carcinoma hereditary spherocytosis influenza intrahepatic cholangiocarcinoma kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver cancer liver disease lung benign neoplasm lung carcinoma lung small cell carcinoma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma thalassemia tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
54659	UDP glucuronosyltransferase family 1 member A3	UGT1A3 Aliases: UGT1C	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis allergic asthma asthma beta thalassemia bilirubin metabolic disorder breast cancer breast carcinoma cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis cryptococcosis diabetes mellitus differentiated thyroid gland carcinoma embryoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis gallbladder disease glycogen storage disease II hepatitis D influenza intrinsic asthma islet cell tumor leukopenia liver disease lung adenocarcinoma lung cancer neonatal jaundice neutropenia obesity pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
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
54579	UDP glucuronosyltransferase family 1 member A5	UGT1A5 Aliases: UGT1E	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 agranulocytosis beta thalassemia bilirubin metabolic disorder cancer carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cryptococcosis diabetes mellitus embryoma epilepsy gallbladder disease glycogen storage disease II hepatitis D influenza leukopenia liver disease neonatal jaundice neutropenia obesity prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia thalassemia type 2 diabetes mellitus visual epilepsy xeroderma pigmentosum group D
54578	UDP glucuronosyltransferase family 1 member A6	UGT1A6 Aliases: GNT1 HLUGP UGT1F	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome abdominal obesity-metabolic syndrome 1 adenocarcinoma adenoma agranulocytosis allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia arteriosclerotic cardiovascular disease asthma atherosclerosis beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease childhood acute lymphocytic leukemia cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma contact dermatitis coronary artery disease cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy female reproductive organ cancer follicular adenoma galactosemia gallbladder disease gastritis 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 disease hemoglobin H disease hepatitis B hepatitis D hepatocellular carcinoma hereditary spherocytosis influenza intrinsic asthma kernicterus due to isoimmunization kernicterus large intestine cancer leukopenia liver cancer liver disease lung benign neoplasm lung cancer lung carcinoma microcystic adenoma neonatal jaundice neutropenia nodular prostate nutmeg liver obesity occupational dermatitis papillary adenoma prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia status epilepticus steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
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
54576	UDP glucuronosyltransferase family 1 member A8	UGT1A8 Aliases: UGT1H	Homo sapiens (human)	Crigler-Najjar syndrome 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 bladder carcinoma breast cancer breast carcinoma cancer carcinoma cardiac arrest cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chronic myeloid leukemia colorectal cancer colorectal carcinoma cryptococcosis cystinuria diabetes mellitus diarrhea differentiated thyroid gland carcinoma embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma female reproductive organ cancer galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease hemoglobin H disease hepatitis D hereditary spherocytosis influenza kernicterus due to isoimmunization kernicterus large intestine cancer leiomyoma leukopenia liver disease myofibroma neonatal jaundice neutropenia nodular prostate obesity prostate cancer prostate carcinoma prostatic adenoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia severe congenital neutropenia sickle cell anemia steatotic liver disease stomach cancer stomach carcinoma thalassemia type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy xeroderma pigmentosum group D
54600	UDP glucuronosyltransferase family 1 member A9	UGT1A9 Aliases: HLUGP4 LUGP4 UGT1AI	Homo sapiens (human)	Crigler-Najjar syndrome Gaucher's disease Gilbert syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Plasmodium falciparum malaria abdominal obesity-metabolic syndrome 1 acute kidney failure adult hepatocellular carcinoma agranulocytosis atopic dermatitis beta thalassemia bilirubin metabolic disorder bladder carcinoma breast cancer cancer carcinoma childhood hepatocellular carcinoma cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptococcosis dermatitis diabetes mellitus diarrhea embryoma epilepsy gallbladder disease glycogen storage disease II hepatitis D hepatocellular carcinoma influenza kidney disease large intestine cancer leukopenia liver cancer liver disease lung cancer lung non-small cell carcinoma neonatal jaundice neutropenia obesity obsolete constipation obsolete dyspepsia prostate cancer prostate carcinoma sarcomatoid carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma stomach cancer thalassemia tongue squamous cell carcinoma type 2 diabetes mellitus urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
10941	UDP glucuronosyltransferase family 2 member A1 complex locus	UGT2A1	Homo sapiens (human)	cancer embryoma laryngeal disease ovarian cancer ovarian carcinoma tracheal disease
574537	UDP glucuronosyltransferase family 2 member A2	UGT2A2	Homo sapiens (human)	ovarian cancer ovarian carcinoma
79799	UDP glucuronosyltransferase family 2 member A3	UGT2A3 Aliases: FLJ21934	Homo sapiens (human)
7365	UDP glucuronosyltransferase family 2 member B10	UGT2B10	Homo sapiens (human)	cancer embryoma prostate cancer prostate carcinoma
10720	UDP glucuronosyltransferase family 2 member B11	UGT2B11	Homo sapiens (human)	cholangiocarcinoma intrahepatic cholangiocarcinoma 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
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
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
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
133688	UDP glycosyltransferase family 3 member A1	UGT3A1 Aliases: FLJ34658	Homo sapiens (human)
167127	UDP glycosyltransferase family 3 member A2	UGT3A2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
10678	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	B3GNT2 Aliases: B3GN-T1 B3GN-T2 B3GNT-2 BETA3GNT	Homo sapiens (human)	Graves' disease Walker-Warburg syndrome acute myocardial infarction cancer congenital muscular dystrophy-dystroglycanopathy type A1 coronary thrombosis hyperthyroidism myocardial infarction parapsoriasis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole schizophrenia silent myocardial infarction thyrotoxicosis transitional cell carcinoma
10331	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3	B3GNT3 Aliases: B3GN-T3 B3GNT-3 HP10328 beta-1,3-N-acetylglucosaminyltransferase bGnT-3 beta3Gn-T3 putative type II membrane protein transmembrane protein 3	Homo sapiens (human)	cancer cervical adenocarcinoma cervical cancer cervix carcinoma common wart embryoma influenza lung cancer lung non-small cell carcinoma neuroblastoma
79369	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4	B3GNT4 Aliases: B3GN-T4 beta3Gn-T4	Homo sapiens (human)
84002	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5	B3GNT5 Aliases: B3GN-T5 beta3Gn-T5 lactosylceramide 1,3-N-acetyl-beta-D-glucosaminyltransferase	Homo sapiens (human)	breast cancer breast carcinoma giant cell glioblastoma glioblastoma

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