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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

Search results for "response to monosaccharide"

Displaying entries **126 - 150** of **733** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
19225	prostaglandin-endoperoxide synthase 2	Ptgs2	Mus musculus (house mouse)
20296	C-C motif chemokine ligand 2	Ccl2	Mus musculus (house mouse)
20317	serine (or cysteine) peptidase inhibitor, clade F, member 1	Serpinf1	Mus musculus (house mouse)
20466	transcriptional regulator, SIN3A (yeast)	Sin3a	Mus musculus (house mouse)
20499	solute carrier family 12, member 7	Slc12a7	Mus musculus (house mouse)
20656	superoxide dismutase 2, mitochondrial	Sod2	Mus musculus (house mouse)
20787	sterol regulatory element binding transcription factor 1	Srebf1	Mus musculus (house mouse)
20807	serum response factor	Srf	Mus musculus (house mouse)
21416	transcription factor 7 like 2, T cell specific, HMG box	Tcf7l2	Mus musculus (house mouse)	breast cancer colorectal cancer diabetes mellitus gestational diabetes obesity pancreatic cancer prostate cancer type 2 diabetes mellitus
21803	transforming growth factor, beta 1	Tgfb1	Mus musculus (house mouse)
21823	tyrosine hydroxylase	Th	Mus musculus (house mouse)
21825	thrombospondin 1	Thbs1	Mus musculus (house mouse)
21872	tight junction protein 1	Tjp1	Mus musculus (house mouse)
21926	tumor necrosis factor	Tnf	Mus musculus (house mouse)	Alzheimer's disease Behcet's disease COVID-19 Cor pulmonale Crohn's disease Fanconi anemia Gaucher's disease Graves ophthalmopathy Graves' disease IgA glomerulonephritis Kawasaki disease Mycobacterium avium complex disease Mycoplasma pneumoniae pneumonia Plasmodium falciparum malaria Sjogren's syndrome Stevens-Johnson syndrome Vogt-Koyanagi-Harada disease Weill-Marchesani syndrome acne acquired immunodeficiency syndrome acute myocardial infarction adult respiratory distress syndrome alcoholic hepatitis amyloidosis anemia anogenital venereal wart anterior uveitis anti-basement membrane glomerulonephritis aortic valve stenosis aplastic anemia aspiration pneumonia asthma atopic dermatitis atrial fibrillation autistic disorder autoimmune hepatitis bacterial pneumonia beta thalassemia brain infarction breast adenocarcinoma breast cancer bronchiectasis bronchopulmonary dysplasia cardiac arrest cardiomyopathy cerebral infarction cervical cancer cholesteatoma of middle ear chorioamnionitis chronic obstructive pulmonary disease cicatricial pemphigoid cochlear disease congenital diaphragmatic hernia congestive heart failure corneal ulcer coronary artery disease coronary restenosis cryoglobulinemia cystic fibrosis cystitis dermatitis herpetiformis dermatitis diabetic angiopathy diabetic neuropathy diabetic retinopathy dilated cardiomyopathy 1H dilated cardiomyopathy disseminated intravascular coagulation encephalitis end stage renal disease endometriosis endophthalmitis epididymitis epilepsy erythema nodosum esophagitis extrinsic allergic alveolitis eye disease farmer's lung gastritis glaucoma heart valve disease hemochromatosis hepatitis A hepatitis B hepatocellular carcinoma hepatopulmonary syndrome hepatorenal syndrome hereditary hemorrhagic telangiectasia herpes zoster hidradenitis suppurativa high grade glioma human immunodeficiency virus infectious disease hypertension hypochromic microcytic anemia impotence inclusion body myopathy with Paget disease of bone and frontotemporal dementia inflammatory bowel disease intermediate uveitis intracranial aneurysm iron deficiency anemia keratoconjunctivitis sicca kidney disease leprosy liver cirrhosis liver disease low tension glaucoma lung disease lung non-small cell carcinoma lupus nephritis lymphopenia malaria metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease mevalonic aciduria middle cerebral artery infarction migraine without aura migraine mixed connective tissue disease mucocutaneous leishmaniasis mucopolysaccharidosis VI multiple myeloma multiple sclerosis muscular dystrophy myelodysplastic syndrome myocardial infarction myositis neutropenia obesity obstructive sleep apnea open-angle glaucoma oral squamous cell carcinoma otitis media ovarian cancer paracoccidioidomycosis peptic esophagitis perinatal necrotizing enterocolitis periodontitis peritonitis periventricular leukomalacia pleurisy portal hypertension pre-eclampsia primary biliary cholangitis primary open angle glaucoma primary sclerosing cholangitis prostate cancer psoriasis psoriatic arthritis pulmonary edema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole radiculopathy renal cell carcinoma renal hypertension retinal detachment rheumatoid arthritis rhinitis root resorption schizophrenia sciatic neuropathy scleritis sensorineural hearing loss severe acute respiratory syndrome sickle cell anemia silicosis skin disease small cell carcinoma spondyloarthropathy status epilepticus systemic lupus erythematosus thalassemia thrombocytopenia toxic shock syndrome trachoma transient cerebral ischemia tuberculosis type 1 diabetes mellitus type 2 diabetes mellitus typhoid fever ulcerative colitis ureteral obstruction uveitis vascular dementia visceral leishmaniasis visual epilepsy vitiligo
22228	uncoupling protein 2 (mitochondrial, proton carrier)	Ucp2	Mus musculus (house mouse)	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
22278	upstream transcription factor 1	Usf1	Mus musculus (house mouse)	cardiovascular system disease type 2 diabetes mellitus
22318	vesicle-associated membrane protein 2	Vamp2	Mus musculus (house mouse)
22329	vascular cell adhesion molecule 1	Vcam1	Mus musculus (house mouse)
23098	sterile alpha and TIR motif containing 1	SARM1 Aliases: KIAA0524 SAMD2 SARM	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis type 6 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 bacterial sepsis central nervous system disease chronic obstructive pulmonary disease disease of metabolism frontotemporal dementia late onset Parkinson's disease lateral sclerosis motor neuron disease nervous system disease neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder
23236	phospholipase C beta 1	PLCB1 Aliases: KIAA0581 PLC-I PLC154 phosphoinositide phospholipase C	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 Hirschsprung's disease Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome West syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult oligodendroglioma amyotrophic lateral sclerosis anaplastic astrocytoma autism spectrum disorder autistic disorder benign epilepsy with centrotemporal spikes bipolar disorder blepharospasm brain disease breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood oligodendroglioma chromosome 17p13.1 deletion syndrome colon adenocarcinoma colon cancer colonic benign neoplasm colorectal cancer coronary aneurysm coronary thrombosis cribriform carcinoma depressive disorder developmental and epileptic encephalopathy 12 developmental and epileptic encephalopathy 1 diabetes mellitus diabetic ketoacidosis early infantile epileptic encephalopathy early myoclonic encephalopathy endometriosis of uterus endometriosis epilepsy essential thrombocythemia fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma infertility juvenile pilocytic astrocytoma large intestine cancer lissencephaly liver cancer major depressive disorder malignant astrocytoma melancholic depression mixed glioma mixed oligodendroglioma-astrocytoma mood disorder myelodysplastic syndrome myocardial infarction myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neuroblastoma neurotic disorder nicotine dependence obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive sleep apnea oligodendroglioma partial motor epilepsy pilocytic astrocytoma poikiloderma with neutropenia prediabetes syndrome primary biliary cholangitis progressive muscular atrophy protoplasmic astrocytoma schizophrenia silent myocardial infarction subependymal giant cell astrocytoma substance abuse substance-related disorder trypanosomiasis tubular adenocarcinoma visual epilepsy
23516	solute carrier family 39 member 14	SLC39A14	Homo sapiens (human)	hypermanganesemia with dystonia 2
24051	sarcoglycan, beta (dystrophin-associated glycoprotein)	Sgcb	Mus musculus (house mouse)
24247	calcium-sensing receptor	Casr	Rattus norvegicus (Norway rat)
24310	angiotensin I converting enzyme	Ace	Rattus norvegicus (Norway rat)
24385	glucokinase	Gck	Rattus norvegicus (Norway rat)	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes glucose metabolism disease hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young obesity permanent neonatal diabetes mellitus steatotic liver disease type 2 diabetes mellitus

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