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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 **26 - 50** of **186** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
176760	putative glucosamine-6-phosphate isomerase	T03F6.3	Caenorhabditis elegans
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
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
177971	6-phosphogluconate dehydrogenase, decarboxylating	T25B9.9	Caenorhabditis elegans
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
189173	Putative alpha-L-fucosidase	W03G11.3	Caenorhabditis elegans	diabetes mellitus diabetic retinopathy fucosidosis type 1 diabetes mellitus type 2 diabetes mellitus
180290	Nucleoside hydrolase	Y43F8C.13	Caenorhabditis elegans
178968	N-acetylgalactosaminide beta-1,3-galactosyltransferase	ZC250.2	Caenorhabditis elegans	Peters plus syndrome
175506	putative galactose-1-phosphate uridylyltransferase	ZK1058.3	Caenorhabditis elegans	classic galactosemia galactosemia
191306	Glycosyltransferase family 92 protein ZK381.2	ZK381.2	Caenorhabditis elegans
176388	putative mannose-6-phosphate isomerase	ZK632.4	Caenorhabditis elegans	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
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
175827	Fructose-bisphosphate aldolase 2	aldo-2	Caenorhabditis elegans	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
175920	Chitobiosyldiphosphodolichol beta-mannosyltransferase	algn-1	Caenorhabditis elegans	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
172855	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	algn-10	Caenorhabditis elegans	long QT syndrome 2 nonsyndromic deafness
176032	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	algn-11	Caenorhabditis elegans	congenital disorder of glycosylation Ip
179185	putative Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase	algn-12	Caenorhabditis elegans	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
179890	N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase	algn-13	Caenorhabditis elegans	developmental and epileptic encephalopathy 36
187398	UDP-N-acetylglucosamine transferase subunit ALG14 homolog	algn-14	Caenorhabditis elegans	congenital myasthenic syndrome 15
173912	Alpha-1,3/1,6-mannosyltransferase ALG2	algn-2	Caenorhabditis elegans	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
175065	Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	algn-3	Caenorhabditis elegans	congenital disorder of glycosylation Id congenital disorder of glycosylation
178822	Dolichyl-phosphate beta-glucosyltransferase;dolichyl-phosphate beta-glucosyltransferase	algn-5	Caenorhabditis elegans	congenital disorder of glycosylation type I polycystic kidney disease
182392	putative dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-6	Caenorhabditis elegans	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
190436	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	algn-7	Caenorhabditis elegans	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
174542	putative dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-8	Caenorhabditis elegans	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease

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