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

Displaying entries **8851 - 8875** of **9988** in total

« First

‹ Prev

…

351

352

353

354

355

356

357

358

359

…

Next ›

Last »
Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
2567	gamma-aminobutyric acid type A receptor subunit gamma3	GABRG3	Homo sapiens (human)
2566	gamma-aminobutyric acid type A receptor subunit gamma2	GABRG2	Homo sapiens (human)
2565	gamma-aminobutyric acid type A receptor subunit gamma1	GABRG1	Homo sapiens (human)
2564	gamma-aminobutyric acid type A receptor subunit epsilon	GABRE	Homo sapiens (human)
2563	gamma-aminobutyric acid type A receptor subunit delta	GABRD	Homo sapiens (human)
2562	gamma-aminobutyric acid type A receptor subunit beta3	GABRB3	Homo sapiens (human)
2561	gamma-aminobutyric acid type A receptor subunit beta2	GABRB2	Homo sapiens (human)
2560	gamma-aminobutyric acid type A receptor subunit beta1	GABRB1	Homo sapiens (human)
2559	gamma-aminobutyric acid type A receptor subunit alpha6	GABRA6	Homo sapiens (human)
2558	gamma-aminobutyric acid type A receptor subunit alpha5	GABRA5	Homo sapiens (human)
2557	gamma-aminobutyric acid type A receptor subunit alpha4	GABRA4	Homo sapiens (human)
2556	gamma-aminobutyric acid type A receptor subunit alpha3	GABRA3	Homo sapiens (human)
2555	gamma-aminobutyric acid type A receptor subunit alpha2	GABRA2	Homo sapiens (human)
2554	gamma-aminobutyric acid type A receptor subunit alpha1	GABRA1	Homo sapiens (human)
2553	GA binding protein transcription factor subunit beta 1	GABPB1	Homo sapiens (human)
2551	GA binding protein transcription factor subunit alpha	GABPA	Homo sapiens (human)
2550	gamma-aminobutyric acid type B receptor subunit 1	GABBR1	Homo sapiens (human)
2549	GRB2 associated binding protein 1	GAB1	Homo sapiens (human)
2548	alpha glucosidase	GAA Aliases: Pompe disease glycogen storage disease type II	Homo sapiens (human)	Becker muscular dystrophy Clouston syndrome Duchenne muscular dystrophy Fabry disease Friedreich ataxia 1 Friedreich ataxia aortic aneurysm ataxia telangiectasia 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 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 cancer cardiomyopathy cerebellar ataxia cerebellar disease chylomicron retention disease cystinuria cytochrome-c oxidase deficiency disease diaphragm disease disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III 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 VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease membranous glomerulonephritis mitochondrial metabolism disease mitochondrial myopathy muscular dystrophy myopathy neurodegenerative disease neuromuscular disease 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 patent foramen ovale peroxisome biogenesis disorder 7A primary immunodeficiency disease sensorineural hearing loss thyroid gland anaplastic carcinoma
2547	X-ray repair cross complementing 6	XRCC6	Homo sapiens (human)
2542	solute carrier family 37 member 4	SLC37A4 Aliases: G6PT GSD1b GSD1c GSD1d Glucose-6-phosphate exchanger SLC37A4 SPX4 glucose-6-phosphatase transporter sugar-phosphate exchange protein 4	Homo sapiens (human)	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome achondroplasia acute pancreatitis agranulocytosis aphthous stomatitis autoimmune disease autoimmune lymphoproliferative syndrome brain cancer cancer central nervous system cancer congenital disorder of glycosylation type II cystinuria diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma essential hypertension eyelid disease familial hyperlipidemia focal segmental glomerulosclerosis galactosemia giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease Ib glycogen storage disease Ic glycogen storage disease gout hepatoblastoma hepatocellular carcinoma high grade glioma hypertension hyperuricemia hypoglycemia immune system disease inherited metabolic disorder kidney disease kidney failure kwashiorkor lactic acidosis leukopenia liver cancer marasmus mixed glioma nephritis nephrolithiasis nephrosis neutropenia nutrition disease obesity obsolete type 1 diabetes mellitus 9 osteoporosis pancreatitis polycystic ovary syndrome primary pulmonary hypertension protein-energy malnutrition proteinuria pyoureter severe congenital neutropenia sudden infant death syndrome 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 uric acid nephrolithiasis xanthomatosis
2539	glucose-6-phosphate dehydrogenase	G6PD Aliases: G6PD1	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 B-cell lymphoma Baraitser-Winter syndrome Bartter disease Bloch-Sulzberger syndrome Burkitt lymphoma Chagas disease Conn's syndrome Creutzfeldt-Jakob disease Duchenne muscular dystrophy Emery-Dreifuss muscular dystrophy Fabry disease Fraser syndrome Gilbert syndrome Goldenhar syndrome IGSF1 deficiency syndrome Japanese encephalitis Langerhans-cell histiocytosis Moebius syndrome Muenke Syndrome Nance-Horan syndrome Native American myopathy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium ovale malaria Plasmodium vivax malaria Renpenning syndrome Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Waterhouse-Friderichsen syndrome Weissenbacher-Zweymuller syndrome Werner syndrome Wilson disease Wiskott-Aldrich syndrome X-linked chronic granulomatous disease abdominal obesity-metabolic syndrome 1 achromatopsia acoustic neuroma acquired color blindness acquired immunodeficiency syndrome acquired polycythemia acute chest syndrome acute kidney failure acute lymphoblastic leukemia acute megakaryocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal adenoma adrenal cortex cancer adrenal gland cancer adrenoleukodystrophy adult acute lymphocytic leukemia adult hepatocellular carcinoma adult lymphoma age related macular degeneration allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia amyloidosis anaplastic astrocytoma anemia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anogenital venereal wart asthma ataxia telangiectasia atypical chronic myeloid leukemia, BCR-ABL1 negative atypical hemolytic-uremic syndrome autistic disorder bacterial sepsis beta thalassemia bilirubin metabolic disorder bipolar disorder bladder carcinoma blastomycosis blood group incompatibility blue color blindness bone marrow cancer borderline personality disorder brain cancer brain ischemia brain stem infarction branchiootic syndrome breast adenocarcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cardiovascular system disease cataract central nervous system cancer central nervous system lymphoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood leukemia childhood lymphoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chromophobe renal cell carcinoma chronic granulomatous disease chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chylomicron retention disease classic galactosemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma common cold common wart conduct disorder cone-rod dystrophy congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia congenital hemolytic anemia congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 congenital nonspherocytic hemolytic anemia congestive heart failure contact dermatitis coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma cutaneous leishmaniasis cystinuria degeneration of macula and posterior pole dementia dengue disease dengue hemorrhagic fever diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism duodenum cancer embryoma endocarditis endomyocardial fibrosis epilepsy epithelioid malignant peripheral nerve sheath tumor erythropoietin polycythemia esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia factor VIII deficiency familial adenomatous polyposis 1 familial adenomatous polyposis familial erythrocytosis 2 familial hyperlipidemia familial periodic paralysis favism fetal erythroblastosis fibrillary astrocytoma fragile X syndrome fundus albipunctatus galactokinase deficiency galactosemia gemistocytic astrocytoma gliosarcoma glomerulonephritis glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart cancer heart disease hematologic cancer hematopoietic system disease hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobin H disease hemoglobinopathy hemoglobinuria hemolytic anemia hemolytic-uremic syndrome hemophilia B hepatic coma hepatic encephalopathy hepatitis A hepatitis B hepatitis hepatoblastoma hepatocellular carcinoma hereditary elliptocytosis hereditary spherocytosis hidradenoma high grade glioma human immunodeficiency virus infectious disease hyperhomocysteinemia hyperparathyroidism hypertension hypertrophic cardiomyopathy hypohidrotic ectodermal dysplasia hypomelanosis of Ito hypothyroidism inherited metabolic disorder intellectual disability intermittent explosive disorder intrinsic asthma iron metabolism disease juvenile pilocytic astrocytoma kernicterus due to isoimmunization kernicterus kidney cancer kidney disease large intestine cancer learning disability leishmaniasis leukemia lingual-facial-buccal dyskinesia lipid storage disease liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macrocytic anemia macular degeneration malaria malignant astrocytoma malignant peripheral nerve sheath tumor melanoma metabolic dysfunction-associated steatotic liver disease methemoglobinemia middle cerebral artery infarction mixed glioma movement disease mucocutaneous leishmaniasis multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myocardial infarction myopathy myxedema neonatal jaundice nephritis nephrogenic diabetes insipidus nephrosis neurilemmoma neuroblastoma neurodegenerative disease neurofibromatosis 1 neurofibromatosis neurofibrosarcoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete subacute myeloid leukemia obsolete ymphosarcoma occupational dermatitis oculocerebrorenal syndrome orofaciodigital syndrome I orofaciodigital syndrome X osteitis fibrosa pancytopenia papillary adenocarcinoma papillary renal cell carcinoma paracoccidioidomycosis parathyroid adenoma parathyroid carcinoma paroxysmal nocturnal hemoglobinuria peroxisome biogenesis disorder 8A phagocyte bactericidal dysfunction phenylketonuria pheochromocytoma pilocytic astrocytoma plasmacytoma pneumocystosis polycythemia vera polycythemia prediabetes syndrome priapism primary hyperaldosteronism primary immunodeficiency disease primary pulmonary hypertension progeria prostate cancer prostate carcinoma protoplasmic astrocytoma psychotic disorder pterygium pyoureter pyruvate kinase deficiency of red cells red color blindness red-green color blindness renal carcinoma renal cell carcinoma renovascular hypertension reticulosarcoma retinitis pigmentosa rhabdomyosarcoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder senile cataract sickle cell anemia silent myocardial infarction skin melanoma skin papilloma skin tag small intestine cancer spondylocarpotarsal synostosis syndrome steatotic liver disease stress polycythemia subependymal giant cell astrocytoma sulfhemoglobinemia syringoma thalassemia thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma transient cerebral ischemia trypanosomiasis tubular adenocarcinoma 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 urinary bladder cancer vascular dementia vascular disease vertebrobasilar insufficiency viral infectious disease visceral leishmaniasis visual epilepsy vitiligo yellow fever
2538	glucose-6-phosphatase catalytic subunit 1	G6PC1 Aliases: GSD1a glycogen storage disease type I, von Gierke disease	Homo sapiens (human)	Fabry disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Laron syndrome Zollinger-Ellison syndrome achondroplasia acute pancreatitis adenocarcinoma adenoma agranulocytosis anemia blood coagulation disease bone marrow cancer breast cancer cancer carcinoma chromophobe renal cell carcinoma chronic kidney disease chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma cystinuria diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma epilepsy essential hypertension eyelid disease familial hyperlipidemia familial periodic paralysis focal segmental glomerulosclerosis follicular adenoma galactosemia gallbladder disease gastrointestinal system disease gestational diabetes giant cell glioblastoma glioblastoma glomerulonephritis glucose intolerance glucose metabolism disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III 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 VI glycogen storage disease VII glycogen storage disease VIII glycogen storage disease gout hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertension hyperuricemia hypoglycemia insulinoma intestinal disease kidney disease kidney failure kwashiorkor lactic acidosis leukopenia lipid storage disease liver cancer liver disease macrocytic anemia marasmus methemoglobinemia microcystic adenoma myeloproliferative neoplasm myopathy nephritis nephrolithiasis nephrosis neuroblastoma neutropenia nonpapillary renal cell carcinoma nutrition disease obesity obsolete type 1 diabetes mellitus 9 osteoporosis ovarian cancer ovarian carcinoma pancreatitis papillary adenoma papillary renal cell carcinoma placental insufficiency polycystic ovary syndrome prediabetes syndrome protein-energy malnutrition proteinuria pyoureter renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma severe congenital neutropenia steatotic liver disease sudden infant death syndrome sulfhemoglobinemia 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 uterine corpus cancer visual epilepsy xanthomatosis
2537	interferon alpha inducible protein 6	IFI6	Homo sapiens (human)
2535	frizzled class receptor 2	FZD2	Homo sapiens (human)

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

International Collaboration

Acknowledgements