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
173171	UDP-glucose 4-epimerase	gale-1	galactose epimerase deficiency galactosemia thrombocytopenia
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
179755	UDP-glucuronosyltransferase	ugt-6
179759	UDP-glucuronosyltransferase	ugt-18
183462	UDP-glucuronosyltransferase	ugt-15
181205	UDP-glucuronosyltransferase	ugt-23
174145	UDP-sugar transporter sqv-7	sqv-7	schneckenbecken dysplasia
174243	Uncharacterized protein	B0495.5	oligoasthenoteratozoospermia
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
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
185403	Uncharacterized protein	F37A4.3
176633	Uracil-DNA glycosylase	ung-1	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
176077	Uridine and thymidine phosphorylase	upp-1	middle cerebral artery infarction
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
190099	Xylosyltransferase sqv-6;protein xylosyltransferase	sqv-6	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
174705	Zinc finger transcription factor pqm-1	pqm-1
187799	glucuronosyltransferase	ugt-59
180119	glycogenin glucosyltransferase	gyg-2	glycogen storage disease XV glycogen storage disease
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
173393	putative ADP-dependent glucokinase	C50D2.7
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
176557	putative N-acetylgalactosaminyltransferase 9	gly-9
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

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