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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 **421451 - 421475** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
2571	glutamate decarboxylase 1	GAD1	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 Down syndrome Graves' disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Raynaud disease Reye syndrome Stiff-Person syndrome Sveinsson chorioretinal atrophy Wernicke-Korsakoff syndrome acquired immunodeficiency syndrome acute lymphoblastic leukemia adamantinous craniopharyngioma adult acute lymphocytic leukemia adult respiratory distress syndrome agoraphobia alcohol dependence alcohol use disorder alternating hemiplegia of childhood amnestic disorder amphetamine abuse androgen insensitivity syndrome anthracosilicosis antisocial personality disorder anxiety disorder arteriosclerotic cardiovascular disease asbestosis atherosclerosis atrophic gastritis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autonomic neuropathy basal ganglia disease bipolar disorder borderline personality disorder bronchus cancer bronchus carcinoma cancer cardiovascular system disease celiac disease central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration cerebral palsy childhood acute lymphocytic leukemia chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft lip cleft palate cocaine abuse cocaine dependence collecting duct carcinoma colorectal cancer complex partial epilepsy congenital nystagmus congestive heart failure coronary artery disease craniopharyngioma delusional disorder depressive disorder developmental and epileptic encephalopathy 89 diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of mental health dissociated nystagmus dissociative amnesia drug psychosis dysthymic disorder dystonia embryoma encephalitis encephalomyelitis endocrine system disease epilepsy focal epilepsy focal hand dystonia gastric adenocarcinoma generalized anxiety disorder generalized dystonia gestational diabetes gliosarcoma glomerulonephritis glucose intolerance glutaric acidemia I goiter heart disease hemiplegia hemophilia B heroin dependence herpes simplex high grade glioma human immunodeficiency virus infectious disease hyperglycemia hyperlysinemia hyperprolactinemia hyperthyroidism hypochondriasis immune system disease influenza insulinoma intellectual disability intermittent explosive disorder isolated cleft palate kidney disease learning disability lingual-facial-buccal dyskinesia locked-in syndrome lung adenocarcinoma lung cancer lung carcinoma major depressive disorder maturity-onset diabetes of the young melancholic depression microcephaly microphthalmia middle cerebral artery infarction migraine mixed glioma mood disorder morphine dependence multiple sclerosis myelitis nephritis nephrosis nervous system disease neuroblastoma neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neuropathy neurotic disorder newborn respiratory distress syndrome nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete constipation obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea opiate dependence pancreatic cancer pancreatic carcinoma panic disorder papillary craniopharyngioma papillary renal cell carcinoma partial motor epilepsy pathologic nystagmus periodontitis peripheral nervous system disease personality disorder phobic disorder pityriasis rubra pilaris pneumoconiosis pneumocystosis polyneuropathy post-traumatic stress disorder prediabetes syndrome primary cerebellar degeneration progressive multifocal leukoencephalopathy prostate adenocarcinoma prostate cancer prostate carcinoma psychotic disorder pyoureter quadriplegia renal carcinoma renal cell carcinoma retrograde amnesia sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scoliosis seasonal affective disorder sickle cell anemia siderosis social phobia spastic cerebral palsy spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus stereotypic movement disorder substance abuse substance-related disorder temporal lobe epilepsy thyroid gland disease thyrotoxicosis transient cerebral ischemia trypanosomiasis 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 visual epilepsy withdrawal disorder
2570	gamma-aminobutyric acid type A receptor subunit rho2	GABRR2	Homo sapiens (human)
2569	gamma-aminobutyric acid type A receptor subunit rho1	GABRR1	Homo sapiens (human)
2568	gamma-aminobutyric acid type A receptor subunit pi	GABRP	Homo sapiens (human)
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

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