GlyCosmos Portal

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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 ▼
182392	putative dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-6	Caenorhabditis elegans	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
178364	putative phosphomannomutase	F52B11.2	Caenorhabditis elegans	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congenital disorder of glycosylation
176736	Polypeptide N-acetylgalactosaminyltransferase 5	gly-5	Caenorhabditis elegans	colorectal cancer
3564879	Sulfotransferase domain-containing protein	hst-3.2	Caenorhabditis elegans	colon cancer hereditary angioedema lung cancer lung non-small cell carcinoma pancreatic cancer
175506	putative galactose-1-phosphate uridylyltransferase	ZK1058.3	Caenorhabditis elegans	classic galactosemia galactosemia
173114	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3	gly-15	Caenorhabditis elegans	cataract 13 with adult i phenotype cataract
173109	GLYcosylation related	gly-16	Caenorhabditis elegans	cataract 13 with adult i phenotype cataract
179562	Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-20	Caenorhabditis elegans	carbohydrate metabolic disorder congenital disorder of glycosylation type IIa
176388	putative mannose-6-phosphate isomerase	ZK632.4	Caenorhabditis elegans	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
3565968	Alpha-(1,3)-fucosyltransferase fut-5	fut-5	Caenorhabditis elegans	candidiasis
187342	Fucosyltransferase	fut-4	Caenorhabditis elegans	candidiasis
188084	Alpha-(1,3)-fucosyltransferase fut-6	fut-6	Caenorhabditis elegans	candidiasis
3565069	Glycosyltransferase 25 family member	D2045.9	Caenorhabditis elegans	brain small vessel disease 3
186765	Poly(ADP-ribose) glycohydrolase 2	parg-2	Caenorhabditis elegans	borna disease brain infarction stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
177683	Poly(ADP-ribose) glycohydrolase 1;poly(ADP-ribose) glycohydrolase	parg-1	Caenorhabditis elegans	borna disease brain infarction stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
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
181517	putative beta-mannosidase	C33G3.4	Caenorhabditis elegans	beta-mannosidosis
185454	Protein O-mannosyl-transferase F38B6.6	F38B6.6	Caenorhabditis elegans	autosomal recessive nonsyndromic deafness
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	Caenorhabditis elegans	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
175827	Fructose-bisphosphate aldolase 2	aldo-2	Caenorhabditis elegans	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
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
176455	Glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	C38H2.2	Caenorhabditis elegans	autoimmune disease of blood
178080	Exostosin-1 homolog	rib-1	Caenorhabditis elegans	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
176000	UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase;protein O-GlcNAc transferase	ogt-1	Caenorhabditis elegans	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
175502	ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase;NAD(+) hydrolase tir-1;Sterile alpha and TIR motif-containing protein 1	tir-1	Caenorhabditis elegans	amyotrophic lateral sclerosis neurodegenerative disease

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