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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

Displaying entries **76 - 100** of **186** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▼
172232	Adenine phosphoribosyltransferase;adenine phosphoribosyltransferase	aprt-1	Caenorhabditis elegans	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
180628	putative endochitinase	cht-1	Caenorhabditis elegans	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease cryptococcosis endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia silicosis sinusitis small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
177235	2-oxoglutarate dehydrogenase, mitochondrial;Transketolase-like pyrimidine-binding domain-containing protein	ogdh-1	Caenorhabditis elegans	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
180533	Beta-hexosaminidase A	hex-1	Caenorhabditis elegans	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
178046	Glucose-6-phosphate 1-dehydrogenase	gspd-1	Caenorhabditis elegans	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
178968	N-acetylgalactosaminide beta-1,3-galactosyltransferase	ZC250.2	Caenorhabditis elegans	Peters plus syndrome
171965	putative phosphoglycerate kinase	pgk-1	Caenorhabditis elegans	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
174131	Sphingomyelin phosphodiesterase 1	asm-1	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
176879	Putative sphingomyelin phosphodiesterase asm-3;Sphingomyelin phosphodiesterase	asm-3	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
181323	Sphingomyelin phosphodiesterase 2	asm-2	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
174924	Glycogen [starch] synthase	gsy-1	Caenorhabditis elegans	Lafora disease cardiovascular system disease glycogen storage disease
190668	Beta-1,4-N-acetylgalactosaminyltransferase bre-4	bre-4	Caenorhabditis elegans	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease multiple sclerosis
173574	Putative glucosylceramidase 1	gba-1	Caenorhabditis elegans	Gaucher's disease type I Gaucher's disease type II Gaucher's disease Lewy body dementia Parkinson's disease
183155	Putative glucosylceramidase 2	gba-2	Caenorhabditis elegans	Gaucher's disease type I Gaucher's disease type II Gaucher's disease Lewy body dementia Parkinson's disease
178535	Putative glucosylceramidase 3	gba-3	Caenorhabditis elegans	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Netherton syndrome Parkinson's disease Parkinsonism late onset Parkinson's disease psoriasis
177314	Putative glucosylceramidase 4	gba-4	Caenorhabditis elegans	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Netherton syndrome Parkinson's disease Parkinsonism late onset Parkinson's disease psoriasis
189104	Uncharacterized protein	W02B3.4	Caenorhabditis elegans	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
173469	Fukutin;Nucleotidyltransferase family protein	T07D3.4	Caenorhabditis elegans	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
188207	Uncharacterized protein	T07A5.1	Caenorhabditis elegans	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
173635	Beta-1,3-galactosyltransferase sqv-2	sqv-2	Caenorhabditis elegans	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Caenorhabditis elegans	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
259529	GDP-fucose protein O-fucosyltransferase 2	pad-2	Caenorhabditis elegans	Down syndrome
180607	GDP-fucose protein O-fucosyltransferase 1	pfut-1	Caenorhabditis elegans	Dowling-Degos disease
177675	Heparan sulfate N-sulfotransferase 1	hst-1	Caenorhabditis elegans	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
190099	Xylosyltransferase sqv-6;protein xylosyltransferase	sqv-6	Caenorhabditis elegans	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus

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