GlyCosmos Portal

Caenorhabditis elegans

Summary

Taxonomy ID: 6239
PubChem Taxonomy: 6239

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

Displaying entries **151 - 175** of **186** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
174705	Zinc finger transcription factor pqm-1	pqm-1
174633	Alpha-1,2-mannosyltransferase algn-9	algn-9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
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
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
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
174517	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase sqv-8	sqv-8	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia
174507	Putative UDP-glucuronosyltransferase ugt-58	ugt-58
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
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
174243	Uncharacterized protein	B0495.5	oligoasthenoteratozoospermia
174145	UDP-sugar transporter sqv-7	sqv-7	schneckenbecken dysplasia
174131	Sphingomyelin phosphodiesterase 1	asm-1	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
174001	Ceramide glucosyltransferase 3	cgt-3	hypertension
173958	Alpha-(1,3)-fucosyltransferase fut-3	fut-3
173912	Alpha-1,3/1,6-mannosyltransferase ALG2	algn-2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
173911	Putative deoxyribose-phosphate aldolase	F09E5.3
173747	putative glycerol kinase	R11F4.1	familial hypercholesterolemia glycerol kinase deficiency
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
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
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
173405	Chitin synthase chs-2;chitin synthase	chs-2
173393	putative ADP-dependent glucokinase	C50D2.7
173171	UDP-glucose 4-epimerase	gale-1	galactose epimerase deficiency galactosemia thrombocytopenia
173114	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3	gly-15	cataract 13 with adult i phenotype cataract
173109	GLYcosylation related	gly-16	cataract 13 with adult i phenotype cataract

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