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 ▲
183155	Putative glucosylceramidase 2	gba-2	Gaucher's disease type I Gaucher's disease type II Gaucher's disease Lewy body dementia Parkinson's disease
190668	Beta-1,4-N-acetylgalactosaminyltransferase bre-4	bre-4	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease multiple sclerosis
174924	Glycogen [starch] synthase	gsy-1	Lafora disease cardiovascular system disease glycogen storage disease
174131	Sphingomyelin phosphodiesterase 1	asm-1	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
176879	Putative sphingomyelin phosphodiesterase asm-3;Sphingomyelin phosphodiesterase	asm-3	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
181323	Sphingomyelin phosphodiesterase 2	asm-2	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
171965	putative phosphoglycerate kinase	pgk-1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
178968	N-acetylgalactosaminide beta-1,3-galactosyltransferase	ZC250.2	Peters plus syndrome
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
180533	Beta-hexosaminidase A	hex-1	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
177235	2-oxoglutarate dehydrogenase, mitochondrial;Transketolase-like pyrimidine-binding domain-containing protein	ogdh-1	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
180628	putative endochitinase	cht-1	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease cryptococcosis endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia silicosis sinusitis small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
172232	Adenine phosphoribosyltransferase;adenine phosphoribosyltransferase	aprt-1	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
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
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
178080	Exostosin-1 homolog	rib-1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
176455	Glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	C38H2.2	autoimmune disease of blood
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
175827	Fructose-bisphosphate aldolase 2	aldo-2	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
185454	Protein O-mannosyl-transferase F38B6.6	F38B6.6	autosomal recessive nonsyndromic deafness
181517	putative beta-mannosidase	C33G3.4	beta-mannosidosis
176437	putative citrate synthase, mitochondrial	cts-1	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
186765	Poly(ADP-ribose) glycohydrolase 2	parg-2	borna disease brain infarction stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
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

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