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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 "carbohydrate metabolic process"

Displaying entries **276 - 300** of **78965** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
10317	beta-1,3-galactosyltransferase 5	B3GALT5 Aliases: B3GalT-V B3T5 GLCT5 GlcNAc-beta-1,3-galactosyltransferase 5 beta3Gal-T5 homolog of C. elegans Bt toxin resistance gene bre-5	Homo sapiens (human)	acute myeloid leukemia adenocarcinoma adenoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cribriform carcinoma granular cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer pancreatic cancer pancreatic carcinoma tubular adenocarcinoma
10327	aldo-keto reductase family 1 member A1	AKR1A1 Aliases: ALR DD3 aldehyde reductase dihydrodiol dehydrogenase 3	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 Barrett's esophagus Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prinzmetal angina Reye syndrome Stargardt disease Wernicke-Korsakoff syndrome acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adrenoleukodystrophy adult fibrosarcoma age related macular degeneration alcohol dependence alcohol use disorder alcoholic hepatitis alcoholic liver cirrhosis alcoholic pancreatitis amnestic disorder anaplastic astrocytoma anorectal stricture arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation atrophy of testis autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome background diabetic retinopathy benign ependymoma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone osteosarcoma brain cancer brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis cardiovascular system disease cellular ependymoma cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood cerebral astrocytoma childhood ependymoma childhood osteosarcoma cholangiocarcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy dysthymic disorder embryoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential tremor exudative vitreoretinopathy familial periodic paralysis fibrillary astrocytoma fibrosarcoma gallbladder disease gastric cardia adenocarcinoma gemistocytic astrocytoma glucocorticoid-remediable aldosteronism glycogen storage disease II granular cell carcinoma granuloma annulare head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hypopharynx cancer immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease intrahepatic cholangiocarcinoma juvenile pilocytic astrocytoma kwashiorkor large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal disease larynx cancer liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macular degeneration major depressive disorder malaria malignant astrocytoma marasmus melancholic depression migraine myocardial infarction myopathy myxopapillary ependymoma neurodegenerative disease neuropathy neurotic disorder nicotine dependence non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete constipation obsolete eye and adnexa disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oral candidiasis osteoporosis osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary ependymoma papillary renal cell carcinoma perinatal necrotizing enterocolitis peripheral nervous system disease pharynx cancer pilocytic astrocytoma placental insufficiency polyneuropathy proliferative diabetic retinopathy prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma renal carcinoma renal cell carcinoma reticulosarcoma sarcomatoid renal cell carcinoma schizophrenia scurvy sensorineural hearing loss silent myocardial infarction squamous cell carcinoma squamous cell neoplasm steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma substance abuse substance-related disorder tanycytic ependymoma tongue squamous cell carcinoma tracheal disease 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 viral infectious disease vulvovaginal candidiasis
10402	ST3 beta-galactoside alpha-2,3-sialyltransferase 6	ST3GAL6 Aliases: ST3GALVI	Homo sapiens (human)	cancer carcinoma colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer multiple myeloma sarcomatoid carcinoma stomach cancer
10559	solute carrier family 35 member A1	SLC35A1 Aliases: CMP-Sia-Tr CMP-sialic acid transporter CMPST hCST	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 Behcet's disease Marfan syndrome Papillon-Lefevre disease Pick's disease Reye syndrome acute myocardial infarction agranulocytosis amyotrophic lateral sclerosis anhidrosis anterior horn cell disease aortic valve insufficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain disease brain stem infarction cancer cardiovascular system disease cellulitis central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cone-rod dystrophy 2 cone-rod dystrophy congenital disorder of glycosylation Iq congenital disorder of glycosylation type II congenital disorder of glycosylation type IIf congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diabetic macular edema dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma glucose intolerance heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability lateral sclerosis learning disability lingual-facial-buccal dyskinesia liver cancer microcephaly mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 neutropenia obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pathologic nystagmus placental insufficiency pneumonia prediabetes syndrome progressive bulbar palsy progressive muscular atrophy proteinuria severe congenital neutropenia silent myocardial infarction situs inversus spontaneous ocular nystagmus substance abuse substance-related disorder thrombocytopenia tuberous sclerosis 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 ulcerative colitis viral infectious disease visual epilepsy
10690	fucosyltransferase 9	FUT9 Aliases: Fuc-TIX alpha (1,3) fucosyltransferase	Homo sapiens (human)	bronchus cancer bronchus carcinoma cancer candidiasis colorectal cancer colorectal carcinoma embryoma hepatocellular carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma malaria
10728	prostaglandin E synthase 3	PTGES3 Aliases: TEBP cPGES p23	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 Creutzfeldt-Jakob disease Lyme disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adult fibrosarcoma alexia aortic valve insufficiency atherosclerosis autism spectrum disorder autistic disorder bone osteosarcoma breast cancer breast carcinoma cancer carcinoma cerebral degeneration childhood acute lymphocytic leukemia childhood osteosarcoma cribriform carcinoma cryptosporidiosis cystic fibrosis diarrhea dyslexia embryoma esophageal cancer esophageal carcinoma familial retinoblastoma fibrosarcoma granular cell carcinoma hepatitis C intrahepatic cholestasis of pregnancy lung adenocarcinoma lung cancer lung non-small cell carcinoma neurodegenerative disease oligodendroglioma osteosarcoma papillary adenocarcinoma papillary renal cell carcinoma periodontitis prostate cancer prostate carcinoma retinoblastoma sarcomatoid carcinoma schizophrenia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma thyroid gland papillary carcinoma toxic encephalopathy trilateral retinoblastoma tubular adenocarcinoma
10825	neuraminidase 3	NEU3	Homo sapiens (human)	Tay-Sachs disease alternating hemiplegia of childhood amnestic disorder autonomic neuropathy cancer carcinoma central nervous system disease chromophobe renal cell carcinoma clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dissociative amnesia embryoma giant cell glioblastoma glioblastoma high grade glioma idiopathic interstitial pneumonia large intestine cancer lung cancer lung non-small cell carcinoma nervous system disease ovarian cancer ovarian carcinoma ovarian clear cell adenocarcinoma ovary adenocarcinoma papillary renal cell carcinoma postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pulmonary fibrosis renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma
10891	PPARG coactivator 1 alpha	PPARGC1A	Homo sapiens (human)	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome age related macular degeneration amblyopia amyotrophic lateral sclerosis cardiovascular system disease chronic obstructive pulmonary disease colitis congenital hypothyroidism diabetic retinopathy dilated cardiomyopathy heart disease hyperglycemia hyperthyroidism kidney cancer kidney failure macular degeneration malignant fibrous histiocytoma melanoma metabolic dysfunction-associated steatotic liver disease myocardial infarction nephrotic syndrome obesity placental insufficiency prediabetes syndrome primary biliary cholangitis renal fibrosis sciatic neuropathy steatotic liver disease type 2 diabetes mellitus
10905	mannosidase alpha class 1A member 2	MAN1A2 Aliases: MAN1B	Homo sapiens (human)	hepatocellular carcinoma liver cancer
10993	serine dehydratase	SDS	Homo sapiens (human)
11091	WD repeat domain 5	WDR5	Homo sapiens (human)	congenital heart disease
11164	nudix hydrolase 5	NUDT5 Aliases: YSA1H hYSAH1	Homo sapiens (human)	breast cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
11181	trehalase	TREH Aliases: MGC129621 TRE TREA alpha,alpha-trehalase alpha,alpha-trehalose glucohydrolase	Homo sapiens (human)	adult medulloblastoma autosomal dominant cerebellar ataxia bronchus cancer bronchus carcinoma cancer central nervous system cancer childhood medulloblastoma diabetes mellitus diabetic ketoacidosis diarrhea embryoma familial nephrotic syndrome giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma herpes simplex high grade glioma kidney disease lipoid nephrosis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma medulloblastoma medullomyoblastoma melanotic medulloblastoma mixed glioma nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome optic atrophy 1 optic atrophy pyoureter rheumatoid arthritis spinal cancer steatotic liver disease type 2 diabetes mellitus
11253	mannosidase alpha class 1B member 1	MAN1B1 Aliases: ER alpha 1,2-mannosidase ERMan1 ERManI MANA-ER MRT15 Man9GlcNAc2-specific processing alpha-mannosidase alpha 1,2-mannosidase endoplasmic Reticulum Class I alpha-mannosidase endoplasmic reticulum alpha-mannosidase 1 endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase 1	Homo sapiens (human)	Hailey-Hailey disease Rafiq syndrome Rothmund-Thomson syndrome agnosia alpha 1-antitrypsin deficiency autistic disorder autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bladder carcinoma bulimia nervosa cancer cerebral degeneration choreatic disease congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation cutis laxa depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease hepatocellular carcinoma hyperopia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver disease major depressive disorder mal de Meleda melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia oophoritis parametritis partial motor epilepsy pelvic inflammatory disease periventricular nodular heterotopia pyosalpinx restrictive dermopathy salpingitis stereotypic movement disorder syndactyly syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 urinary bladder cancer visual epilepsy
11285	beta-1,4-galactosyltransferase 7	B4GALT7 Aliases: XGALT-1 beta4Gal-T7 galactosyltransferase I	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Laron syndrome Larsen-like syndrome B3GAT3 type 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 Prader-Willi syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome achondroplasia aortic valve disease 2 aortic valve stenosis arthritis arthropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive Robinow syndrome autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bone disease cartilage disease chondrodysplasia-pseudohermaphroditism syndrome cleidocranial dysplasia clubfoot colitis collagen disease coloboma congenital disorder of glycosylation type IId congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease cryptorchidism cutis laxa enophthalmos gastroenteritis gingivitis hepatocellular carcinoma humeroradial synostosis ileitis ileocolitis lipoatrophic diabetes mellitus lipodystrophy liver cancer mal de Meleda microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mucopolysaccharidosis IV multiple epiphyseal dysplasia obsolete exophthalmos orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis scoliosis skin disease spermatic cord torsion trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
11364	acyl-Coenzyme A dehydrogenase, medium chain	Acadm	Mus musculus (house mouse)	medium chain acyl-CoA dehydrogenase deficiency metabolic dysfunction-associated steatotic liver disease
11450	adiponectin, C1Q and collagen domain containing	Adipoq	Mus musculus (house mouse)	Alzheimer's disease Behcet's disease Crohn's disease Graves' disease Kawasaki disease Mycobacterium avium complex disease Rett syndrome amyloidosis ankylosing spondylitis atherosclerosis autoimmune hepatitis biliary atresia bipolar disorder brain infarction breast cancer cardiomyopathy cardiovascular system disease chronic obstructive pulmonary disease colitis congestive heart failure coronary aneurysm coronary artery disease dementia diabetic retinopathy diffuse scleroderma end stage renal disease familial hyperlipidemia familial mediterranean fever gestational diabetes graft-versus-host disease hepatocellular carcinoma hyperinsulinism hyperthyroidism inflammatory bowel disease liver cirrhosis metabolic dysfunction-associated steatotic liver disease multiple sclerosis myocardial infarction obesity peripheral artery disease polycystic ovary syndrome primary open angle glaucoma proliferative diabetic retinopathy prostate adenocarcinoma pulmonary tuberculosis rheumatoid arthritis sleep apnea steatotic liver disease tongue squamous cell carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vascular disease
11548	adrenergic receptor, alpha 1b	Adra1b	Mus musculus (house mouse)
11554	adrenergic receptor, beta 1	Adrb1	Mus musculus (house mouse)	aortic valve stenosis chronic obstructive pulmonary disease congestive heart failure cystic fibrosis dilated cardiomyopathy hyperglycemia hypertension low tension glaucoma myocardial infarction nephrosclerosis obstructive sleep apnea periodontitis renovascular hypertension type 1 diabetes mellitus
11605	galactosidase, alpha	Gla	Mus musculus (house mouse)
11651	thymoma viral proto-oncogene 1	Akt1	Mus musculus (house mouse)	Cowden syndrome 6 Parkinson's disease Proteus syndrome alcohol use disorder autosomal recessive polycystic kidney disease bipolar disorder brain ischemia breast cancer cancer chronic myeloid leukemia colon cancer colorectal cancer diabetic retinopathy esophageal cancer esophagus squamous cell carcinoma hepatocellular carcinoma hypertension idiopathic pulmonary fibrosis impotence in situ carcinoma intermediate coronary syndrome invasive ductal carcinoma lung non-small cell carcinoma malignant astrocytoma myocardial infarction ovarian cancer pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paraplegia prostate adenocarcinoma prostate cancer pulmonary tuberculosis renal cell carcinoma schizophrenia type 2 diabetes mellitus ureteral obstruction urinary bladder cancer vulva cancer
11652	thymoma viral proto-oncogene 2	Akt2	Mus musculus (house mouse)	Parkinson's disease alcohol use disorder cancer colorectal cancer endometrial cancer hepatocellular carcinoma high grade glioma hypertension hypoglycemia hypoinsulinemic hypoglycemia with hemihypertrophy ischemia malignant astrocytoma obesity ovarian carcinoma polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma type 2 diabetes mellitus
11668	aldehyde dehydrogenase family 1, subfamily A1	Aldh1a1	Mus musculus (house mouse)	obesity pancreatic cancer
11674	aldolase A, fructose-bisphosphate	Aldoa	Mus musculus (house mouse)
11676	aldolase C, fructose-bisphosphate	Aldoc	Mus musculus (house mouse)	autoimmune disease of the nervous system borna disease hepatocellular carcinoma

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