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
174145	UDP-sugar transporter sqv-7	sqv-7	schneckenbecken dysplasia
174243	Uncharacterized protein	B0495.5	oligoasthenoteratozoospermia
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
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
174507	Putative UDP-glucuronosyltransferase ugt-58	ugt-58
174517	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase sqv-8	sqv-8	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia
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
174578	Glyceraldehyde-3-phosphate dehydrogenase 4	gpd-4	Alzheimer's disease brain glioma diabetic retinopathy epilepsy lymphangioleiomyomatosis middle cerebral artery infarction obesity oral squamous cell carcinoma rheumatic heart disease
174603	Glyceraldehyde-3-phosphate dehydrogenase 1	gpd-1	Alzheimer's disease brain glioma diabetic retinopathy epilepsy lymphangioleiomyomatosis middle cerebral artery infarction obesity oral squamous cell carcinoma rheumatic heart disease
174633	Alpha-1,2-mannosyltransferase algn-9	algn-9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
174705	Zinc finger transcription factor pqm-1	pqm-1
174736	GPI mannosyltransferase 1	pigm-1
174924	Glycogen [starch] synthase	gsy-1	Lafora disease cardiovascular system disease glycogen storage disease
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
175453	Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-14
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
175506	putative galactose-1-phosphate uridylyltransferase	ZK1058.3	classic galactosemia galactosemia
175558	Ricin B lectin domain-containing protein;putative N-acetylgalactosaminyltransferase 6	gly-6
175591	UDP-glucuronosyltransferase	ugt-62	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
175827	Fructose-bisphosphate aldolase 2	aldo-2	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
175886	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit stt-3	stt-3	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
175920	Chitobiosyldiphosphodolichol beta-mannosyltransferase	algn-1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
175995	Probable-ribose 5-phosphate isomerase	rpia-1
176000	UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase;protein O-GlcNAc transferase	ogt-1	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
176032	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	algn-11	congenital disorder of glycosylation Ip

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