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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 **9401 - 9425** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
50831	taste 2 receptor member 3	TAS2R3	Homo sapiens (human)
149095	DC-STAMP domain containing 1	DCST1	Homo sapiens (human)
3998	lectin, mannose binding 1	LMAN1 Aliases: ERGIC-53 ERGIC53 FMFD1 MCFD1 MR60 endoplasmic reticulum-golgi intermediate compartment protein 53 gp58	Homo sapiens (human)	IgA glomerulonephritis adenocarcinoma adenoma allergic disease arteriosclerotic cardiovascular disease atherosclerosis blood coagulation disease cancer carcinoma colorectal cancer congenital afibrinogenemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia coronary artery disease factor V deficiency factor VII deficiency factor VIII deficiency factor XIII deficiency follicular adenoma hematopoietic system disease large intestine cancer malaria microcystic adenoma nutmeg liver obsolete inherited blood coagulation disease papillary adenoma sarcomatoid carcinoma thanatophoric dysplasia vitamin K deficiency bleeding
1605	dystroglycan 1	DAG1 Aliases: 156DAG A3a AGRNR DAG alpha-dystroglycan beta-dystroglycan dystrophin-associated glycoprotein-1	Homo sapiens (human)	Alzheimer's disease Becker muscular dystrophy Bethlem myopathy Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Dandy-Walker syndrome Dubowitz syndrome Duchenne muscular dystrophy Ebola hemorrhagic fever Fukuyama congenital muscular dystrophy Joubert syndrome Lassa fever Lyme disease Marfan syndrome Miller-Dieker lissencephaly 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 Peters anomaly Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Walker-Warburg syndrome X-linked Aarskog syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult medulloblastoma agnosia allergic asthma ameloblastoma ankylosing spondylitis anterior horn cell disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 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 Robinow syndrome 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 brain cancer breast cancer breast carcinoma bronchopulmonary dysplasia buphthalmos campomelic dysplasia cancer carcinoma cardiomyopathy cataract celiac disease central nervous system cancer childhood leukemia childhood medulloblastoma childhood type dermatomyositis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer common variable immunodeficiency communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy-dystroglycanopathy type A9 congenital muscular dystrophy congestive heart failure cornea plana coronary artery disease coronary thrombosis cortical dysplasia-focal epilepsy syndrome craniometaphyseal dysplasia cribriform carcinoma cryptorchidism dental caries dentin caries depressive disorder dermatomyositis developmental coordination disorder diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy embryoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma essential hypertension facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy giant cell glioblastoma glaucoma glioblastoma gliosarcoma granular cell carcinoma heart septal defect high grade glioma hydranencephaly hydrocephalus hydrophthalmos hypertension hypertrophic cardiomyopathy immune system disease inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated elevated serum creatine phosphokinase levels juvenile rheumatoid arthritis large intestine cancer learning disability leukemia leukodystrophy limb-girdle muscular dystrophy lissencephaly lymphocytic choriomeningitis major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly microphthalmia mixed glioma muscular atrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia myositis myotonic dystrophy type 1 myotonic dystrophy type 2 neurodegenerative disease neuromuscular disease neuropathy nonpapillary renal cell carcinoma obesity 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 obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma parapsoriasis partial motor epilepsy peripheral nervous system disease polyneuropathy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary biliary cholangitis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole recurrent corneal erosion renal carcinoma renal cell carcinoma retinal detachment rhabdomyosarcoma rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction situs inversus squamous cell carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type systemic lupus erythematosus tongue cancer tongue squamous cell carcinoma tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uterine corpus cancer visual epilepsy
4012	leucyl and cystinyl aminopeptidase	LNPEP	Homo sapiens (human)
790	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	CAD Aliases: GATD4	Homo sapiens (human)
1271	ciliary neurotrophic factor receptor	CNTFR	Homo sapiens (human)	acute lymphoblastic leukemia adult acute lymphocytic leukemia amyotrophic lateral sclerosis attention deficit hyperactivity disorder cancer central nervous system cancer childhood acute lymphocytic leukemia childhood acute myeloid leukemia cold-induced sweating syndrome 1 cold-induced sweating syndrome gliosarcoma high grade glioma idiopathic scoliosis mixed glioma myasthenia gravis progressive muscular atrophy rheumatoid arthritis
283726	stabilizer of axonemal microtubules 2	SAXO2	Homo sapiens (human)
2589	polypeptide N-acetylgalactosaminyltransferase 1	GALNT1 Aliases: GalNAc-T1 polypeptide GalNAc transferase 1 protein-UDP acetylgalactosaminyltransferase 1	Homo sapiens (human)	colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure heart valve disease hepatocellular carcinoma large intestine cancer liver cancer ovarian cancer ovarian carcinoma pulmonary valve stenosis stomach cancer stomach carcinoma
57514	Rho GTPase activating protein 31	ARHGAP31	Homo sapiens (human)
3595	interleukin 12 receptor subunit beta 2	IL12RB2	Homo sapiens (human)
64175	prolyl 3-hydroxylase 1	P3H1	Homo sapiens (human)
39	acetyl-CoA acetyltransferase 2	ACAT2 Aliases: Acetyl-CoA acetyltransferase, cytosolic acetoacetyl Coenzyme A thiolase	Homo sapiens (human)	amyotrophic lateral sclerosis androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis beta-ketothiolase deficiency breast cancer cholecystolithiasis choledocholithiasis cholelithiasis choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease hepatitis C hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease liver cancer nutmeg liver papillary renal cell carcinoma premature menopause progressive muscular atrophy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma syndromic X-linked intellectual disability type 10 ulcerative colitis
1109	aldo-keto reductase family 1 member C4	AKR1C4 Aliases: 3-alpha hydroxysteroid dehydrogenase, type I 3-alpha-HSD C11 CDR DD4 HAKRA MGC22581 chlordecone reductase dihydrodiol dehydrogenase 4	Homo sapiens (human)	46,XY sex reversal 8 46,XY sex reversal 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Marfan syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Pick's disease Reye syndrome Richter's syndrome Sakati-Nyhan syndrome Smith-McCort dysplasia Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome acute myeloid leukemia alcohol dependence alcohol use disorder alopecia amyloidosis androgenic alopecia anemia angle-closure glaucoma bacterial infectious disease bipolar disorder bladder carcinoma branchiootic syndrome breast cancer breast carcinoma cancer cerebral degeneration chikungunya childhood leukemia chronic closed-angle glaucoma chronic lymphocytic leukemia cryptorchidism delusional disorder dementia dengue hemorrhagic fever depressive disorder disorder of sexual development dysthymic disorder embryoma essential hypertension essential thrombocythemia follicular lymphoma glaucoma hepatocellular carcinoma hermaphroditism hypertension hypogonadotropic hypogonadism 23 with or without anosmia influenza leukemia liver cancer liver carcinoma lupus erythematosus macrocytic anemia major depressive disorder melancholic depression myelofibrosis neurotic disorder obsolete melancholia orofaciodigital syndrome I orofaciodigital syndrome X osteoporosis paranoid schizophrenia plasmacytoma polycythemia vera polycythemia primary angle-closure glaucoma primary ciliary dyskinesia 1 primary ciliary dyskinesia pseudohermaphroditism secondary Parkinson disease situs inversus systemic lupus erythematosus tuberous sclerosis urinary bladder cancer viral infectious disease
64218	semaphorin 4A	SEMA4A	Homo sapiens (human)
2039	dematin actin binding protein	DMTN	Homo sapiens (human)
7544	zinc finger protein Y-linked	ZFY	Homo sapiens (human)
57153	solute carrier family 44 member 2 (CTL2 blood group)	SLC44A2	Homo sapiens (human)
25802	leiomodin 1	LMOD1	Homo sapiens (human)
5426	DNA polymerase epsilon, catalytic subunit	POLE Aliases: DNA polymerase epsilon catalytic subunit A POLE1	Homo sapiens (human)
80741	lymphocyte antigen 6 family member G5C	LY6G5C	Homo sapiens (human)
146664	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	MGAT5B Aliases: FLJ25132 GnT-IX GnT-VB	Homo sapiens (human)	brain cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatocellular carcinoma liver cancer neuroblastoma nonpapillary renal cell carcinoma papillary renal cell carcinoma polycystic ovary syndrome renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
23070	cap methyltransferase 1	CMTR1	Homo sapiens (human)
25981	dynein axonemal heavy chain 1	DNAH1	Homo sapiens (human)
5894	Raf-1 proto-oncogene, serine/threonine kinase	RAF1	Homo sapiens (human)

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