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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 **51 - 75** of **186** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
176077	Uridine and thymidine phosphorylase	upp-1	Caenorhabditis elegans	middle cerebral artery infarction
176112	Polypeptide N-acetylgalactosaminyltransferase 3	gly-3	Caenorhabditis elegans	heart valve disease
176149	Phosphorylase b kinase regulatory subunit;putative phosphorylase b kinase regulatory subunit alpha	C14B9.8	Caenorhabditis elegans	glycogen storage disease IXa glycogen storage disease IXd glycogen storage disease hypothyroidism visceral heterotaxy
176231	Chondroitin sulfate synthase mig-22	mig-22	Caenorhabditis elegans
176332	Beta-1,4-mannosyltransferase bre-3	bre-3	Caenorhabditis elegans
176366	Putative UDP-glucuronosyltransferase ugt-60	ugt-60	Caenorhabditis elegans
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Caenorhabditis elegans	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
176388	putative mannose-6-phosphate isomerase	ZK632.4	Caenorhabditis elegans	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
176399	Glycerol-3-phosphate dehydrogenase [NAD(+)];putative glycerol-3-phosphate dehydrogenase 2	gpdh-2	Caenorhabditis elegans	Brugada syndrome 2
176437	putative citrate synthase, mitochondrial	cts-1	Caenorhabditis elegans	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
176453	Orotidine 5'-phosphate decarboxylase	umps-1	Caenorhabditis elegans	orotic aciduria purine-pyrimidine metabolic disorder
176455	Glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	C38H2.2	Caenorhabditis elegans	autoimmune disease of blood
176502	Exostosin-2 homolog	rib-2	Caenorhabditis elegans	hereditary multiple exostoses
176557	putative N-acetylgalactosaminyltransferase 9	gly-9	Caenorhabditis elegans
176633	Uracil-DNA glycosylase	ung-1	Caenorhabditis elegans	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
176647	Putative polypeptide N-acetylgalactosaminyltransferase 11	gly-11	Caenorhabditis elegans
176736	Polypeptide N-acetylgalactosaminyltransferase 5	gly-5	Caenorhabditis elegans	colorectal cancer
176760	putative glucosamine-6-phosphate isomerase	T03F6.3	Caenorhabditis elegans
176788	Fructose-bisphosphate aldolase 1	aldo-1	Caenorhabditis elegans	autoimmune disease of the nervous system borna disease hepatocellular carcinoma hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
176874	Dolichol-phosphate mannosyltransferase subunit 1	dpm-1	Caenorhabditis elegans	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
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
177033	Invertebrate-type lysozyme 3	ilys-3	Caenorhabditis elegans
177164	Invertebrate-type lysozyme 6	ilys-6	Caenorhabditis elegans
177235	2-oxoglutarate dehydrogenase, mitochondrial;Transketolase-like pyrimidine-binding domain-containing protein	ogdh-1	Caenorhabditis elegans	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
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

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