GlyCosmos Portal

Caenorhabditis elegans

Summary

Taxonomy ID: 6239
PubChem Taxonomy: 6239

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

Displaying entries **126 - 150** of **186** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
172305	GPI mannosyltransferase pigv-1	pigv-1	hyperphosphatasia with impaired intellectual development syndrome 1
174736	GPI mannosyltransferase 1	pigm-1
173109	GLYcosylation related	gly-16	cataract 13 with adult i phenotype cataract
259529	GDP-fucose protein O-fucosyltransferase 2	pad-2	Down syndrome
180607	GDP-fucose protein O-fucosyltransferase 1	pfut-1	Dowling-Degos disease
176032	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	algn-11	congenital disorder of glycosylation Ip
178982	GDP-D-glucose phosphorylase 1	mcp-1
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
187342	Fucosyltransferase	fut-4	candidiasis
175827	Fructose-bisphosphate aldolase 2	aldo-2	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
176788	Fructose-bisphosphate aldolase 1	aldo-1	autoimmune disease of the nervous system borna disease hepatocellular carcinoma hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
177363	Fructose-2,6-bisphosphatase	pfkb-1.2	hyperinsulinism
176502	Exostosin-2 homolog	rib-2	hereditary multiple exostoses
178080	Exostosin-1 homolog	rib-1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
174423	Enolase	enol-1	Alzheimer's disease Parkinsonism aortic valve stenosis brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy
187770	Endonuclease III homolog	nth-1	familial adenomatous polyposis 3
179990	EGF domain-specific O-linked N-acetylglucosamine transferase;Heparan N-sulfatase	H12D21.10	Adams-Oliver syndrome
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
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
172855	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	algn-10	long QT syndrome 2 nonsyndromic deafness
172851	Chondroitin sulfate synthase sqv-5;Hexosyltransferase	sqv-5	temtamy preaxial brachydactyly syndrome
176231	Chondroitin sulfate synthase mig-22	mig-22
175920	Chitobiosyldiphosphodolichol beta-mannosyltransferase	algn-1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation

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