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 ▼
172232	Adenine phosphoribosyltransferase;adenine phosphoribosyltransferase	aprt-1	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
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
177235	2-oxoglutarate dehydrogenase, mitochondrial;Transketolase-like pyrimidine-binding domain-containing protein	ogdh-1	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
180533	Beta-hexosaminidase A	hex-1	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
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
178968	N-acetylgalactosaminide beta-1,3-galactosyltransferase	ZC250.2	Peters plus syndrome
171965	putative phosphoglycerate kinase	pgk-1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
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
174924	Glycogen [starch] synthase	gsy-1	Lafora disease cardiovascular system disease glycogen storage 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
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
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
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
177314	Putative glucosylceramidase 4	gba-4	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
189104	Uncharacterized protein	W02B3.4	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
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
188207	Uncharacterized protein	T07A5.1	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
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
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
259529	GDP-fucose protein O-fucosyltransferase 2	pad-2	Down syndrome
180607	GDP-fucose protein O-fucosyltransferase 1	pfut-1	Dowling-Degos disease
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
190099	Xylosyltransferase sqv-6;protein xylosyltransferase	sqv-6	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus

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