GlyCosmos Portal

Caenorhabditis elegans

Summary

Taxonomy ID: 6239
PubChem Taxonomy: 6239

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

Displaying entries **1 - 25** of **186** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
179674	Transketolase-like pyrimidine-binding domain-containing protein;putative 2-oxoglutarate dehydrogenase E1 component DHKTD1 homolog, mitochondrial	ogdh-2	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
179990	EGF domain-specific O-linked N-acetylglucosamine transferase;Heparan N-sulfatase	H12D21.10	Adams-Oliver syndrome
266823	Poly [ADP-ribose] polymerase;Poly [ADP-ribose] polymerase 1	parp-1	Alzheimer's disease Huntington's disease Parkinson's disease arthritis asthma autoimmune disease bacterial meningitis borna disease congestive heart failure idiopathic pulmonary fibrosis kidney failure leiomyoma liver cirrhosis middle cerebral artery infarction nephritis perinatal necrotizing enterocolitis stomach cancer stomach carcinoma transient cerebral ischemia type 2 diabetes mellitus ureteral obstruction
183000	Glutathione transferase omega-1	gsto-1	Alzheimer's disease Parkinson's disease asthma
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
180601	Glyceraldehyde-3-phosphate dehydrogenase 3	gpd-3	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
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
174517	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase sqv-8	sqv-8	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia
176399	Glycerol-3-phosphate dehydrogenase [NAD(+)];putative glycerol-3-phosphate dehydrogenase 2	gpdh-2	Brugada syndrome 2
183002	Putative galactocerebrosidase	C29E4.10	Creutzfeldt-Jakob disease Krabbe disease Mycoplasma pneumoniae pneumonia melanoma
185500	UDP-glucuronosyltransferase	ugt-61	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer
175591	UDP-glucuronosyltransferase	ugt-62	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
190099	Xylosyltransferase sqv-6;protein xylosyltransferase	sqv-6	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
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
180607	GDP-fucose protein O-fucosyltransferase 1	pfut-1	Dowling-Degos disease
259529	GDP-fucose protein O-fucosyltransferase 2	pad-2	Down syndrome
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
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
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
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
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

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