GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **1 - 25** of **750** in total

1

2

3

4

5

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
1285	collagen type IV alpha 3 chain	COL4A3	Homo sapiens (human)	Alport syndrome autosomal dominant Alport syndrome autosomal recessive Alport syndrome benign familial hematuria end stage renal disease
54209	triggering receptor expressed on myeloid cells 2	TREM2	Homo sapiens (human)	Alzheimer's disease 17
29527	prostaglandin-endoperoxide synthase 2	Ptgs2	Rattus norvegicus (Norway rat)	Alzheimer's disease Barrett's esophagus Huntington's disease Parkinsonism Wernicke encephalopathy acute kidney failure adenocarcinoma brain ischemia cystitis diabetic neuropathy endometriosis gastric ulcer gastritis hypertension lung cancer nephrotic syndrome pleurisy polycystic kidney disease portal hypertension pulmonary emphysema pulmonary hypertension retrograde amnesia secondary hyperparathyroidism status epilepticus steatotic liver disease ulcerative colitis
3383	intercellular adhesion molecule 1	ICAM1 Aliases: BB2 CD54 human rhinovirus receptor	Homo sapiens (human)	Alzheimer's disease Behcet's disease Crohn's disease Graves ophthalmopathy Graves' disease biliary atresia diabetic retinopathy inflammatory bowel disease iridocyclitis liver cirrhosis malaria multiple myeloma prostate cancer psoriasis skin melanoma type 1 diabetes mellitus
7124	tumor necrosis factor	TNF	Homo sapiens (human)	Alzheimer's disease Behcet's disease Gaucher's disease Graves ophthalmopathy Graves' disease Kawasaki disease Sjogren's syndrome acne adult respiratory distress syndrome anterior uveitis aplastic anemia asthma atopic dermatitis bacterial pneumonia beta thalassemia breast adenocarcinoma breast cancer bronchopulmonary dysplasia cerebral infarction cervical cancer chorioamnionitis chronic obstructive pulmonary disease coronary artery disease coronary restenosis cystic fibrosis dermatitis herpetiformis dermatitis diabetic angiopathy diabetic retinopathy erythema nodosum esophagitis extrinsic allergic alveolitis farmer's lung hemochromatosis hepatitis B hepatocellular carcinoma hidradenitis suppurativa high grade glioma hypertension hypochromic microcytic anemia intermediate uveitis iron deficiency anemia leprosy liver disease low tension glaucoma lung non-small cell carcinoma malaria metabolic dysfunction and alcohol associated liver disease migraine without aura migraine mucocutaneous leishmaniasis multiple myeloma multiple sclerosis neutropenia obstructive sleep apnea open-angle glaucoma paracoccidioidomycosis pre-eclampsia primary open angle glaucoma prostate cancer psoriasis psoriatic arthritis pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis pustulosis of palm and sole renal cell carcinoma rheumatoid arthritis rhinitis schizophrenia scleritis sensorineural hearing loss silicosis skin disease systemic lupus erythematosus thrombocytopenia trachoma type 1 diabetes mellitus typhoid fever uveitis vascular dementia visceral leishmaniasis visual epilepsy
3552	interleukin 1 alpha	IL1A	Homo sapiens (human)	Alzheimer's disease Fabry disease Schnitzler syndrome acute myeloid leukemia asthma autoimmune thrombocytopenic purpura end stage renal disease graft-versus-host disease interstitial lung disease iridocyclitis juvenile rheumatoid arthritis keratoconus lung non-small cell carcinoma multiple myeloma osteoporosis pulmonary fibrosis rheumatoid arthritis type 1 diabetes mellitus
83516	PPARG coactivator 1 alpha	Ppargc1a	Rattus norvegicus (Norway rat)	Alzheimer's disease Huntington's disease colitis diabetic retinopathy dilated cardiomyopathy heart disease hyperglycemia kidney failure metabolic dysfunction-associated steatotic liver disease obesity sciatic neuropathy steatotic liver disease type 2 diabetes mellitus
2752	glutamate-ammonia ligase	GLUL Aliases: glutamine synthetase	Homo sapiens (human)	Alzheimer's disease Huntington's disease congenital glutamine deficiency developmental and epileptic encephalopathy 116 heart disease
6648	superoxide dismutase 2	SOD2	Homo sapiens (human)	Alzheimer's disease Kuhnt-Junius degeneration Leber hereditary optic neuropathy acute myeloid leukemia alcoholic liver cirrhosis asthma bilirubin metabolic disorder breast cancer cardiomyopathy carotid artery disease diabetic angiopathy dilated cardiomyopathy hepatocellular carcinoma hypertension inclusion body myositis infectious mononucleosis liver cirrhosis lung cancer metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease multiple myeloma neuronal ceroid lipofuscinosis optic neuritis osteoporosis ovarian cancer pancreatic cancer polyneuropathy primary open angle glaucoma pseudoxanthoma elasticum reactive arthritis stomach cancer systemic lupus erythematosus type 1 diabetes mellitus type 2 diabetes mellitus vitiligo
25608	leptin	Lep	Rattus norvegicus (Norway rat)	Alzheimer's disease Parkinson's disease alcohol dependence alcoholic liver cirrhosis glucose intolerance hepatocellular carcinoma hyperinsulinism hypertension hypogonadism obesity osteoporosis short bowel syndrome type 2 diabetes mellitus
25718	insulin-like growth factor 1 receptor	Igf1r	Rattus norvegicus (Norway rat)	Alzheimer's disease Parkinson's disease prostate adenocarcinoma
24310	angiotensin I converting enzyme	Ace	Rattus norvegicus (Norway rat)	Alzheimer's disease abdominal aortic aneurysm acute kidney failure autosomal recessive polycystic kidney disease bronchiolitis obliterans congestive heart failure diastolic heart failure end stage renal disease focal segmental glomerulosclerosis 1 glomerulonephritis glomerulosclerosis hypertension leukostasis lung disease middle cerebral artery infarction myocardial infarction myocarditis nephrosis nephrotic syndrome ocular hypotension osteoporosis pre-malignant neoplasm proteinuria pulmonary fibrosis renal fibrosis renovascular hypertension ureteral obstruction
4023	lipoprotein lipase	LPL	Homo sapiens (human)	Alzheimer's disease coronary artery disease familial combined hyperlipidemia familial hyperlipidemia familial lipoprotein lipase deficiency hypertension muscular disease myocardial infarction type 2 diabetes mellitus
5465	peroxisome proliferator activated receptor alpha	PPARA	Homo sapiens (human)	Alzheimer's disease coronary artery disease hepatocellular carcinoma lipid metabolism disorder myocardial infarction
5105	phosphoenolpyruvate carboxykinase 1	PCK1 Aliases: PEPCK-C	Homo sapiens (human)	Alzheimer's disease type 2 diabetes mellitus
1636	angiotensin I converting enzyme	ACE Aliases: ACE1 CD143 peptidyl-dipeptidase A	Homo sapiens (human)	Behcet's disease COVID-19 Coronavirus infectious disease Fabry disease IgA glomerulonephritis IgA vasculitis allergic disease anemia ankylosing spondylitis aspiration pneumonia asthma atrial fibrillation breast cancer cerebral infarction chronic obstructive pulmonary disease coronary artery disease diabetic retinopathy diastolic heart failure end stage renal disease familial Mediterranean fever gallbladder adenocarcinoma heart valve disease hepatitis A hepatocellular carcinoma hypertension leukemia liver cirrhosis lung cancer mitral valve disease mitral valve prolapse multiple myeloma myocardial infarction nephritis non-arteritic anterior ischemic optic neuropathy obstructive sleep apnea pneumonia polycythemia pre-eclampsia proteinuria sarcoidosis stomach cancer subacute sclerosing panencephalitis toxic shock syndrome type 1 diabetes mellitus type 2 diabetes mellitus
7040	transforming growth factor beta 1	TGFB1	Homo sapiens (human)	Behcet's disease Camurati-Engelmann disease aphthous stomatitis aplastic anemia asthma atopic dermatitis berylliosis breast cancer chronic obstructive pulmonary disease colon adenocarcinoma cystic fibrosis eosinophilic esophagitis factor VIII deficiency inflammatory bowel disease lung disease multiple myeloma myocardial infarction osteochondrodysplasia pulmonary emphysema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis renal cell carcinoma tracheal stenosis uveitis
3673	integrin subunit alpha 2	ITGA2	Homo sapiens (human)	Behcet's disease Glanzmann's thrombasthenia arteriosclerosis diabetes mellitus diabetic retinopathy intermediate coronary syndrome iron deficiency anemia myocardial infarction retinal vein occlusion sensorineural hearing loss thrombocytopenia thrombosis type 2 diabetes mellitus von Willebrand's disease 1 von Willebrand's disease 2
1292	collagen type VI alpha 2 chain	COL6A2	Homo sapiens (human)	Bethlem myopathy Ullrich congenital muscular dystrophy 1B
1293	collagen type VI alpha 3 chain	COL6A3	Homo sapiens (human)	Bethlem myopathy Ullrich congenital muscular dystrophy 1C chronic kidney disease communication disorder dystonia 27 hypertension muscular dystrophy myocardial infarction primary open angle glaucoma uterine fibroid
5290	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	PIK3CA Aliases: PI3K	Homo sapiens (human)	CLOVES syndrome Cowden syndrome 5 breast angiosarcoma breast cancer cerebral cavernous malformation colon adenocarcinoma colorectal cancer colorectal carcinoma cutaneous Paget's disease epidermal nevus estrogen-receptor positive breast cancer hepatocellular carcinoma lung cancer ovarian cancer rectal benign neoplasm seborrheic keratosis stomach cancer
18706	phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha	Pik3ca	Mus musculus (house mouse)	CLOVES syndrome breast cancer
1277	collagen type I alpha 1 chain	COL1A1	Homo sapiens (human)	Caffey disease Ehlers-Danlos syndrome arthrochalasia type 1 aggressive periodontitis beta thalassemia cutaneous leishmaniasis degenerative disc disease dentinogenesis imperfecta dermatofibrosarcoma protuberans osteogenesis imperfecta type 1 osteogenesis imperfecta type 2 osteogenesis imperfecta type 3 osteogenesis imperfecta type 4 osteogenesis imperfecta osteoporosis otosclerosis
20656	superoxide dismutase 2, mitochondrial	Sod2	Mus musculus (house mouse)	Canavan disease Leigh disease amyotrophic lateral sclerosis type 1 congestive heart failure dilated cardiomyopathy
5165	pyruvate dehydrogenase kinase 3	PDK3	Homo sapiens (human)	Charcot-Marie-Tooth disease X-linked dominant 6

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

International Collaboration

Acknowledgements