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
171965	putative phosphoglycerate kinase	pgk-1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
172008	Orotate phosphoribosyltransferase	R12E2.11	orotic aciduria purine-pyrimidine metabolic disorder
172232	Adenine phosphoribosyltransferase;adenine phosphoribosyltransferase	aprt-1	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
172305	GPI mannosyltransferase pigv-1	pigv-1	hyperphosphatasia with impaired intellectual development syndrome 1
172360	Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	gly-2	proteinuria
172376	2,3-bisphosphoglycerate-independent phosphoglycerate mutase	ipgm-1
172475	Glycosyltransferase family 92 protein;Glycosyltransferase family 92 protein F13G3.3	F13G3.3
172508	Chitin synthase chs-1	chs-1
172509	putative glycerol-3-phosphate dehydrogenase, mitochondrial	gpdh-3	type 2 diabetes mellitus
172851	Chondroitin sulfate synthase sqv-5;Hexosyltransferase	sqv-5	temtamy preaxial brachydactyly syndrome
172855	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	algn-10	long QT syndrome 2 nonsyndromic deafness
173109	GLYcosylation related	gly-16	cataract 13 with adult i phenotype cataract
173114	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3	gly-15	cataract 13 with adult i phenotype cataract
173171	UDP-glucose 4-epimerase	gale-1	galactose epimerase deficiency galactosemia thrombocytopenia
173393	putative ADP-dependent glucokinase	C50D2.7
173405	Chitin synthase chs-2;chitin synthase	chs-2
173469	Fukutin;Nucleotidyltransferase family protein	T07D3.4	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
173574	Putative glucosylceramidase 1	gba-1	Gaucher's disease type I Gaucher's disease type II Gaucher's disease Lewy body dementia Parkinson's disease
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
173747	putative glycerol kinase	R11F4.1	familial hypercholesterolemia glycerol kinase deficiency
173911	Putative deoxyribose-phosphate aldolase	F09E5.3
173912	Alpha-1,3/1,6-mannosyltransferase ALG2	algn-2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
173958	Alpha-(1,3)-fucosyltransferase fut-3	fut-3
174001	Ceramide glucosyltransferase 3	cgt-3	hypertension
174131	Sphingomyelin phosphodiesterase 1	asm-1	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease

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