GlyCosmos Portal

Caenorhabditis elegans

Summary

Taxonomy ID: 6239
PubChem Taxonomy: 6239

Genes (186) Glycans (3) Glycoproteins (1454) Lectins (39) Pathways (499)

Displaying entries **1 - 25** of **186** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
172376	2,3-bisphosphoglycerate-independent phosphoglycerate mutase	ipgm-1
177235	2-oxoglutarate dehydrogenase, mitochondrial;Transketolase-like pyrimidine-binding domain-containing protein	ogdh-1	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
177971	6-phosphogluconate dehydrogenase, decarboxylating	T25B9.9
175502	ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase;NAD(+) hydrolase tir-1;Sterile alpha and TIR motif-containing protein 1	tir-1	amyotrophic lateral sclerosis neurodegenerative disease
180583	ATP-dependent 6-phosphofructokinase 1	pfk-1.1	disease of metabolism glycogen storage disease VII glycogen storage disease
179335	ATP-dependent 6-phosphofructokinase 2	pfk-1.2	disease of metabolism glycogen storage disease VII glycogen storage disease
172232	Adenine phosphoribosyltransferase;adenine phosphoribosyltransferase	aprt-1	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
181778	Alpha,alpha-trehalose-phosphate synthase [UDP-forming] 1	tps-1
3565050	Alpha,alpha-trehalose-phosphate synthase [UDP-forming] 2;Trehalose-6-phosphate phosphatase C-terminal domain-containing protein	tps-2
173958	Alpha-(1,3)-fucosyltransferase fut-3	fut-3
3565968	Alpha-(1,3)-fucosyltransferase fut-5	fut-5	candidiasis
188084	Alpha-(1,3)-fucosyltransferase fut-6	fut-6	candidiasis
178985	Alpha-(1,6)-fucosyltransferase	fut-8	pulmonary emphysema
174633	Alpha-1,2-mannosyltransferase algn-9	algn-9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
175453	Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-14
181005	Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-12
173912	Alpha-1,3/1,6-mannosyltransferase ALG2	algn-2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
179562	Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-20	carbohydrate metabolic disorder congenital disorder of glycosylation type IIa
172360	Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	gly-2	proteinuria
3565692	B3GNT1, Beta-1,3-N-acetylGucosamiNylTransferase 1, homolog	bgnt-1.5	congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
182795	B3GNT1, Beta-1,3-N-acetylGucosamiNylTransferase 1, homolog;Glyco_trans_2-like domain-containing protein	bgnt-1.4	congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
173114	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3	gly-15	cataract 13 with adult i phenotype cataract
189753	Beta-1,3-galactosyltransferase bre-2;Hexosyltransferase	bre-2
178142	Beta-1,3-galactosyltransferase bre-5;Hexosyltransferase	bre-5	pancreatic cancer
173635	Beta-1,3-galactosyltransferase sqv-2	sqv-2	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1

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