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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	July 8, 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 "glycosyltransferase activity"

Displaying entries **426 - 450** of **140293** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
57704	glucosylceramidase beta 2	GBA2 Aliases: AD035 DKFZp762K054 KIAA1605 bile acid beta-glucosidase glucocerebrosidase 2 non-lysosomal glucosylceramidase	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 Gaucher's disease Henoch-Schoenlein purpura Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease MASA syndrome Mast syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease SPOAN syndrome Troyer syndrome alternating hemiplegia of childhood autonomic neuropathy cancer cataract central nervous system disease cerebellar ataxia cerebellar disease cerebral degeneration congenital nystagmus cystic fibrosis dementia dissociated nystagmus glaucoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis infertility intellectual disability learning disability male infertility nervous system disease paraplegia pathologic nystagmus scoliosis sensorineural hearing loss spontaneous ocular nystagmus trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
58193	exostosin-like glycosyltransferase 2	Extl2	Mus musculus (house mouse)
58924	fucosyltransferase 2	Fut2	Rattus norvegicus (Norway rat)	vitamin B12 deficiency
59027	nicotinamide phosphoribosyltransferase	Nampt	Mus musculus (house mouse)	carotid artery disease coronary artery disease kidney failure metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction obesity periodontitis psoriasis pulmonary hypertension transient cerebral ischemia type 2 diabetes mellitus
59048	C1GALT1-specific chaperone 1	C1galt1c1	Mus musculus (house mouse)	Tn polyagglutination syndrome hemolytic-uremic syndrome
60433	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Rfng	Rattus norvegicus (Norway rat)
60507	queuine tRNA-ribosyltransferase catalytic subunit 1	Qtrt1	Mus musculus (house mouse)
60670	fucosyltransferase 4	Fut4	Rattus norvegicus (Norway rat)	candidiasis
63867	UDP glucuronosyltransferase family 2 member A1	Ugt2a1	Rattus norvegicus (Norway rat)
63888	alpha 1,4-galactosyltransferase	A4galt	Rattus norvegicus (Norway rat)
63917	polypeptide N-acetylgalactosaminyltransferase 11	GALNT11 Aliases: GalNAc-T11 polypeptide GalNAc transferase 11	Homo sapiens (human)	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
64016	queuine tRNA-ribosyltransferase catalytic subunit 1	Qtrt1	Rattus norvegicus (Norway rat)
64035	glycogen phosphorylase L	Pygl	Rattus norvegicus (Norway rat)	glycogen storage disease VI glycogen storage disease lactic acidosis
64043	glucosaminyl (N-acetyl) transferase 1	Gcnt1	Rattus norvegicus (Norway rat)
64131	xylosyltransferase 1	XYLT1 Aliases: PXYLT1 XT-I protein xylosyltransferase 1	Homo sapiens (human)	Barber-Say syndrome Bernard-Soulier syndrome Brooke-Spiegler syndrome Desbuquois dysplasia Duchenne muscular dystrophy Ehlers-Danlos syndrome Laron syndrome abdominal aortic aneurysm achondroplasia acne acute myeloid leukemia age related macular degeneration anaplastic astrocytoma angioid streaks anodontia arthritis arthropathy cerebral infarction cerebrovascular disease childhood cerebral astrocytoma chondrodysplasia punctata cleft palate cleidocranial dysplasia clubfoot congestive heart failure degeneration of macula and posterior pole degenerative disc disease diabetes mellitus diabetic ketoacidosis enophthalmos essential hypertension fibrillary astrocytoma gemistocytic astrocytoma glaucoma glomerulonephritis high grade glioma humeroradial synostosis hypertension hypertrichosis hypotrichosis intellectual disability intermittent claudication isolated cleft palate isolated growth hormone deficiency juvenile pilocytic astrocytoma keratosis follicularis kidney disease kidney failure learning disability macular degeneration malignant astrocytoma microcephaly mitral valve insufficiency mitral valve prolapse mitral valve stenosis mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia muscular dystrophy myopia nephritis nephrosis obsolete exophthalmos obsolete type 1 diabetes mellitus 9 orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pilocytic astrocytoma placental insufficiency pleomorphic adenoma postural orthostatic tachycardia syndrome protoplasmic astrocytoma pseudoxanthoma elasticum pyoureter qualitative platelet defect radioulnar synostosis restrictive cardiomyopathy scoliosis subependymal giant cell astrocytoma substance abuse substance-related disorder tooth agenesis 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 ventricular septal defect
64132	xylosyltransferase 2	XYLT2 Aliases: PXYLT2 XT-II protein xylosyltransferase 2	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Desbuquois dysplasia Dubowitz syndrome Ewing sarcoma Gilbert syndrome Meckel syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome T-cell acute lymphoblastic leukemia X-linked Aarskog syndrome acute biphenotypic leukemia acute leukemia acute myocardial infarction age related macular degeneration amblyopia angioid streaks 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 Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome bacterial infectious disease bilirubin metabolic disorder bladder carcinoma blindness brain stem infarction cancer cannabis abuse cannabis dependence cataract cerebral artery occlusion cerebral infarction cerebrovascular disease cholera chondrodysplasia-pseudohermaphroditism syndrome chronic kidney disease chronic monocytic leukemia chronic myelomonocytic leukemia clubfoot congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congestive heart failure coronary thrombosis degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dysthymic disorder embryoma essential hypertension gallbladder disease glomerulonephritis hepatic veno-occlusive disease hepatitis B herpes simplex hypertension intellectual disability intermittent claudication juvenile myelomonocytic leukemia keratosis follicularis kidney disease kidney failure learning disability lichen disease lipoatrophic diabetes mellitus lipodystrophy liver disease localized scleroderma macular degeneration major depressive disorder melancholic depression microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microphthalmia mitral valve insufficiency mitral valve prolapse mitral valve stenosis mongolian spot myocardial infarction myopia nephritis nephrosis neurotic disorder obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 osteoporosis papilloma patent foramen ovale pathologic nystagmus pleomorphic adenoma pneumocystosis polycystic kidney disease postural orthostatic tachycardia syndrome pseudoxanthoma elasticum psoriatic arthritis pyoureter restrictive cardiomyopathy retinal detachment scleroderma sensorineural hearing loss silent myocardial infarction skin benign neoplasm skin cancer spontaneous ocular nystagmus squamous cell papilloma steatotic liver disease strabismic amblyopia systemic scleroderma thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric 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 urinary bladder cancer ventricular septal defect viral infectious disease xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
64133	xylosyltransferase 1	Xylt1	Rattus norvegicus (Norway rat)	Desbuquois dysplasia kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
64134	xylosyltransferase 2	Xylt2	Rattus norvegicus (Norway rat)	polycystic kidney disease pseudoxanthoma elasticum
64383	sirtuin 2	Sirt2	Mus musculus (house mouse)	cocaine dependence high grade glioma intermittent claudication metabolic dysfunction-associated steatotic liver disease
64409	polypeptide N-acetylgalactosaminyltransferase 17	GALNT17 Aliases: GALNTL3 GalNAc-T17 GalNAc-T19 GalNAc-T5L polypeptide GalNAc transferase 3 polypeptide N-acetylgalactosaminyltransferase-like 3 ppGalNAc-T17	Homo sapiens (human)	allergic asthma asthma autism spectrum disorder autistic disorder intrinsic asthma
64442	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	St3gal2	Rattus norvegicus (Norway rat)
64445	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	Rattus norvegicus (Norway rat)	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
64544	beta-1,3-glucuronyltransferase 2	B3gat2	Rattus norvegicus (Norway rat)	Barrett's esophagus schizophrenia
64761	poly(ADP-ribose) polymerase family member 12	PARP12 Aliases: ARTD12 FLJ22693 PARP-12 ZC3H1	Homo sapiens (human)	Zika fever age related macular degeneration cancer coronary artery disease degeneration of macula and posterior pole hepatocellular carcinoma influenza liver cancer macular degeneration viral infectious disease vitiligo
64828	beta-1,4-N-acetyl-galactosaminyl transferase 1	B4galnt1	Rattus norvegicus (Norway rat)	hereditary spastic paraplegia 26

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