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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 **6726 - 6750** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
7384	ubiquinol-cytochrome c reductase core protein 1	UQCRC1	Homo sapiens (human)
7380	uroplakin 3A	UPK3A	Homo sapiens (human)
7379	uroplakin 2	UPK2	Homo sapiens (human)
7378	uridine phosphorylase 1	UPP1 Aliases: UDRPASE UPASE UPP	Homo sapiens (human)	Stevens-Johnson syndrome allergic contact dermatitis breast cancer cancer colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy embryoma esophagus squamous cell carcinoma giardiasis large intestine cancer lung adenoma middle cerebral artery infarction placental insufficiency stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tuberculosis type 2 diabetes mellitus
7375	ubiquitin specific peptidase 4	USP4	Homo sapiens (human)
7374	uracil DNA glycosylase	UNG Aliases: HIGM4 UDG UNG1 UNG2 uracil-DNA glycosylase 1, uracil-DNA glycosylase 2	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 Bloom syndrome CD40 ligand deficiency Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia X-linked hyper IgM syndrome acquired immunodeficiency syndrome acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute myeloid leukemia adult acute lymphocytic leukemia age related macular degeneration bronchus cancer bronchus carcinoma cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cryptosporidiosis degeneration of macula and posterior pole denture stomatitis distal arthrogryposis dysgammaglobulinemia embryoma epididymitis esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma giant cell glioblastoma glioblastoma hepatitis B hepatocellular carcinoma herpes simplex high grade glioma human immunodeficiency virus infectious disease hyper IgM syndrome immunodeficiency with hyper IgM type 3 immunodeficiency with hyper IgM type 5 immunodeficiency with hyper-IgM type 2 large intestine cancer leishmaniasis leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macular degeneration neurodegenerative disease obsolete ymphosarcoma primary immunodeficiency disease prostate cancer prostate carcinoma rheumatoid arthritis squamous cell carcinoma stomatitis tongue squamous cell carcinoma ulcerative stomatitis visceral leishmaniasis
7373	collagen type XIV alpha 1 chain	COL14A1	Homo sapiens (human)
7372	uridine monophosphate synthetase	UMPS Aliases: orotate phosphoribosyl transferase and orotidine-5'-decarboxylase	Homo sapiens (human)	Diamond-Blackfan anemia Gilbert syndrome agranulocytosis anemia basal cell carcinoma beta thalassemia bile duct adenocarcinoma bile duct carcinoma bilirubin metabolic disorder bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carbamoyl phosphate synthetase I deficiency disease carcinoma carpal tunnel syndrome cholangiocarcinoma colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypoplastic anemia coronary artery disease diarrhea disease of metabolism embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma gastrointestinal system cancer gonorrhea hepatocellular carcinoma hereditary spherocytosis intellectual disability intrahepatic cholangiocarcinoma large intestine cancer learning disability leukopenia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia malaria megaloblastic anemia neutropenia orotic aciduria pancreatic cancer pancreatic carcinoma patent ductus arteriosus prostate cancer prostate carcinoma prostatic adenoma purine-pyrimidine metabolic disorder rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma sebaceous carcinoma severe congenital neutropenia sickle cell anemia squamous cell carcinoma stomach cancer stomach carcinoma sweat gland cancer thalassemia tongue squamous cell carcinoma tuberculosis urinary bladder cancer
7371	uridine-cytidine kinase 2	UCK2	Homo sapiens (human)
7369	uromodulin	UMOD Aliases: Tamm-Horsfall glycoprotein uromucoid	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 IgA glomerulonephritis Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Senior-Loken syndrome Van der Woude syndrome abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute myeloid leukemia acute pancreatitis adenine phosphoribosyltransferase deficiency adult acute lymphocytic leukemia alcohol dependence alcohol use disorder anxiety disorder aortic aneurysm arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autoimmune hepatitis autosomal dominant polycystic kidney disease autosomal recessive polycystic kidney disease babesiosis bladder carcinoma breast cancer breast carcinoma cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia chronic interstitial cystitis chronic kidney disease chronic pyelonephritis chylomicron retention disease cleidocranial dysplasia cocaine abuse cocaine dependence congestive heart failure coronary artery disease cystic kidney disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diffuse large B-cell lymphoma esophageal cancer esophageal carcinoma essential hypertension familial juvenile hyperuricemic nephropathy gallbladder disease generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance gout heart disease hepatitis A hepatitis humeroradial synostosis hypertension hyperuricemia interstitial cystitis interstitial nephritis kidney disease kidney failure leukemia lipid storage disease liver cirrhosis liver disease lupus erythematosus maple syrup urine disease middle cerebral artery infarction morphine dependence nephritis nephrolithiasis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis normal pressure hydrocephalus nutmeg liver obsolete type 1 diabetes mellitus 9 osteoporosis ovarian cancer ovarian carcinoma pancreatitis pertussis phobic disorder polycystic kidney disease 1 polycystic kidney disease 4 polydactyly prediabetes syndrome pyelitis pyelonephritis pyoureter radioulnar synostosis renal hypertension renal infectious disease secondary hyperparathyroidism systemic lupus erythematosus 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 uremia uric acid nephrolithiasis urinary bladder cancer urinary tract obstruction
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
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
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
7365	UDP glucuronosyltransferase family 2 member B10	UGT2B10	Homo sapiens (human)	cancer embryoma prostate cancer prostate carcinoma
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
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
7360	UDP-glucose pyrophosphorylase 2	UGP2 Aliases: SVUGP2 UGPP1 UTP--glucose-1-phosphate uridylyltransferase	Homo sapiens (human)	cancer central nervous system cancer classic galactosemia cystinuria developmental and epileptic encephalopathy 83 galactokinase deficiency galactosemia giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma paroxysmal nonkinesigenic dyskinesia 1
7358	UDP-glucose 6-dehydrogenase	UGDH Aliases: GDH UDP-GlcDH UDPGDH UGD uridine-diphospho glucose dehydrogenase	Homo sapiens (human)	Graves' disease Laron syndrome Zollinger-Ellison syndrome achondroplasia beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cholangiocarcinoma developmental and epileptic encephalopathy 84 diarrhea enophthalmos giant cell glioblastoma giardiasis glioblastoma hepatocellular carcinoma high grade glioma hyperinsulinism hyperthyroidism hypoglycemia intrahepatic cholangiocarcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma obsolete exophthalmos orbital disease peripheral artery disease placental insufficiency primary hyperoxaluria thalassemia thyrotoxicosis
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
7355	solute carrier family 35 member A2	SLC35A2 Aliases: UDP-Gal-Tr UDP-galactose translocator UGAT UGT UGT1 UGT2 UGTL	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 Barrett's esophagus Crigler-Najjar syndrome Dandy-Walker syndrome Gilbert syndrome Laron syndrome Pick's disease Reye syndrome West syndrome abdominal obesity-metabolic syndrome 1 achondroplasia adult lymphoma agranulocytosis alternating exotropia anisometropia aromatase excess syndrome autosomal recessive chronic granulomatous disease 1 bacterial infectious disease beta thalassemia bilirubin metabolic disorder bladder carcinoma brain disease breast cancer breast carcinoma cancer carcinoma central nervous system lymphoma central sleep apnea cerebral degeneration childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis chronic granulomatous disease clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIm congenital disorder of glycosylation congenital nystagmus craniosynostosis cryptococcosis cyclic hematopoiesis cystinuria developmental and epileptic encephalopathy 36 diarrhea dissociated nystagmus embryoma epilepsy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esotropia exotropia galactosemia gallbladder disease gastroesophageal reflux disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatitis B hepatitis C hepatitis D hyperopia hypertropia hypoglycemia intellectual disability large intestine cancer learning disability leukopenia liver disease lymphoma macular corneal dystrophy mechanical strabismus microcephaly monocular esotropia monocular exotropia neonatal jaundice neutropenia obsolete constipation obsolete infantile epileptic encephalopathy obsolete ymphosarcoma obstructive sleep apnea ophthalmoplegia ovarian cancer ovarian carcinoma pathologic nystagmus peptic esophagitis placental insufficiency primary cutaneous amyloidosis prostate cancer prostate carcinoma pyloric stenosis sarcomatoid carcinoma scoliosis sensorineural hearing loss severe congenital neutropenia sickle cell anemia spontaneous ocular nystagmus steatotic liver disease strabismus syndromic X-linked intellectual disability 94 tetralogy of Fallot thalassemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome urinary bladder cancer visual epilepsy xeroderma pigmentosum group D
7353	ubiquitin recognition factor in ER associated degradation 1	UFD1	Homo sapiens (human)
7352	uncoupling protein 3	UCP3	Homo sapiens (human)
7351	uncoupling protein 2	UCP2	Homo sapiens (human)	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
7348	uroplakin 1B	UPK1B	Homo sapiens (human)
7343	upstream binding transcription factor	UBTF	Homo sapiens (human)

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