GlyCosmos Portal

Caenorhabditis elegans

Summary

Taxonomy ID: 6239
PubChem Taxonomy: 6239

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

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

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
187770	Endonuclease III homolog	nth-1	familial adenomatous polyposis 3
176633	Uracil-DNA glycosylase	ung-1	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
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
189173	Putative alpha-L-fucosidase	W03G11.3	diabetes mellitus diabetic retinopathy fucosidosis type 1 diabetes mellitus type 2 diabetes mellitus
13184808	Mannosyltransferase	pigb-1	developmental and epileptic encephalopathy 80 sleeping sickness
179890	N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase	algn-13	developmental and epileptic encephalopathy 36
187398	UDP-N-acetylglucosamine transferase subunit ALG14 homolog	algn-14	congenital myasthenic syndrome 15
187206	Glycosyltransferase-like protein LARGE	lge-1	congenital muscular dystrophy-dystroglycanopathy type A6 facioscapulohumeral muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B6
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
177998	Mannosyl-oligosaccharide glucosidase	mogs-1	congenital disorder of glycosylation type IIb
180302	Polypeptide N-acetylgalactosaminyltransferase 4;polypeptide N-acetylgalactosaminyltransferase	gly-4	congenital disorder of glycosylation type II
178822	Dolichyl-phosphate beta-glucosyltransferase;dolichyl-phosphate beta-glucosyltransferase	algn-5	congenital disorder of glycosylation type I polycystic kidney disease
175886	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit stt-3	stt-3	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
176032	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	algn-11	congenital disorder of glycosylation Ip
174633	Alpha-1,2-mannosyltransferase algn-9	algn-9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
175920	Chitobiosyldiphosphodolichol beta-mannosyltransferase	algn-1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
190436	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	algn-7	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
173912	Alpha-1,3/1,6-mannosyltransferase ALG2	algn-2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
174542	putative dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
179185	putative Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase	algn-12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
179218	Mannose-P-dolichol utilization defect 1 protein homolog	mpdu-1	congenital disorder of glycosylation If
176874	Dolichol-phosphate mannosyltransferase subunit 1	dpm-1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
175065	Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	algn-3	congenital disorder of glycosylation Id congenital disorder of glycosylation

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