GlyCosmos Portal

Displaying entries **126 - 150** of **186** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
176453	Orotidine 5'-phosphate decarboxylase	umps-1	orotic aciduria purine-pyrimidine metabolic disorder
176437	putative citrate synthase, mitochondrial	cts-1	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
176399	Glycerol-3-phosphate dehydrogenase [NAD(+)];putative glycerol-3-phosphate dehydrogenase 2	gpdh-2	Brugada syndrome 2
176388	putative mannose-6-phosphate isomerase	ZK632.4	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
176366	Putative UDP-glucuronosyltransferase ugt-60	ugt-60
176332	Beta-1,4-mannosyltransferase bre-3	bre-3
176231	Chondroitin sulfate synthase mig-22	mig-22
176149	Phosphorylase b kinase regulatory subunit;putative phosphorylase b kinase regulatory subunit alpha	C14B9.8	glycogen storage disease IXa glycogen storage disease IXd glycogen storage disease hypothyroidism visceral heterotaxy
176112	Polypeptide N-acetylgalactosaminyltransferase 3	gly-3	heart valve disease
176077	Uridine and thymidine phosphorylase	upp-1	middle cerebral artery infarction
176032	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	algn-11	congenital disorder of glycosylation Ip
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
175995	Probable-ribose 5-phosphate isomerase	rpia-1
175920	Chitobiosyldiphosphodolichol beta-mannosyltransferase	algn-1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
175886	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit stt-3	stt-3	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
175827	Fructose-bisphosphate aldolase 2	aldo-2	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
175591	UDP-glucuronosyltransferase	ugt-62	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
175558	Ricin B lectin domain-containing protein;putative N-acetylgalactosaminyltransferase 6	gly-6
175506	putative galactose-1-phosphate uridylyltransferase	ZK1058.3	classic galactosemia galactosemia
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
175453	Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-14
175065	Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	algn-3	congenital disorder of glycosylation Id congenital disorder of glycosylation
174924	Glycogen [starch] synthase	gsy-1	Lafora disease cardiovascular system disease glycogen storage disease
174736	GPI mannosyltransferase 1	pigm-1

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