GlyCosmos Portal

Caenorhabditis elegans

Summary

Taxonomy ID: 6239
PubChem Taxonomy: 6239

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

Displaying entries **76 - 100** of **186** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
177363	Fructose-2,6-bisphosphatase	pfkb-1.2	hyperinsulinism
177464	Chitinase-like protein C25A8.4	cht-3
177675	Heparan sulfate N-sulfotransferase 1	hst-1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
177683	Poly(ADP-ribose) glycohydrolase 1;poly(ADP-ribose) glycohydrolase	parg-1	borna disease brain infarction stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
177971	6-phosphogluconate dehydrogenase, decarboxylating	T25B9.9
177998	Mannosyl-oligosaccharide glucosidase	mogs-1	congenital disorder of glycosylation type IIb
178046	Glucose-6-phosphate 1-dehydrogenase	gspd-1	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
178080	Exostosin-1 homolog	rib-1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
178131	Queuine tRNA-ribosyltransferase catalytic subunit	tgt-1
178142	Beta-1,3-galactosyltransferase bre-5;Hexosyltransferase	bre-5	pancreatic cancer
178343	Putative polypeptide N-acetylgalactosaminyltransferase 10;Ricin B lectin domain-containing protein	gly-10
178364	putative phosphomannomutase	F52B11.2	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congenital disorder of glycosylation
178535	Putative glucosylceramidase 3	gba-3	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Netherton syndrome Parkinson's disease Parkinsonism late onset Parkinson's disease psoriasis
178583	Malate synthase	icl-1
178623	Poly [ADP-ribose] polymerase tankyrase	tank-1
178661	Polypeptide N-acetylgalactosaminyltransferase;Ricin B lectin domain-containing protein;putative N-acetylgalactosaminyltransferase 7	gly-7
178772	Lysozyme-like protein 7	lys-7
178822	Dolichyl-phosphate beta-glucosyltransferase;dolichyl-phosphate beta-glucosyltransferase	algn-5	congenital disorder of glycosylation type I polycystic kidney disease
178832	TPR_REGION domain-containing protein;dolichyl-phosphate-mannose--protein mannosyltransferase	F32D1.3
178940	Putative UDP-glucuronosyltransferase ugt-48	ugt-48
178968	N-acetylgalactosaminide beta-1,3-galactosyltransferase	ZC250.2	Peters plus syndrome
178982	GDP-D-glucose phosphorylase 1	mcp-1
178985	Alpha-(1,6)-fucosyltransferase	fut-8	pulmonary emphysema
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

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