GlyCosmos Portal

Displaying entries **51 - 75** of **186** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
176077	Uridine and thymidine phosphorylase	upp-1	middle cerebral artery infarction
176112	Polypeptide N-acetylgalactosaminyltransferase 3	gly-3	heart valve disease
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
176231	Chondroitin sulfate synthase mig-22	mig-22
176332	Beta-1,4-mannosyltransferase bre-3	bre-3
176366	Putative UDP-glucuronosyltransferase ugt-60	ugt-60
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
176388	putative mannose-6-phosphate isomerase	ZK632.4	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
176399	Glycerol-3-phosphate dehydrogenase [NAD(+)];putative glycerol-3-phosphate dehydrogenase 2	gpdh-2	Brugada syndrome 2
176437	putative citrate synthase, mitochondrial	cts-1	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
176453	Orotidine 5'-phosphate decarboxylase	umps-1	orotic aciduria purine-pyrimidine metabolic disorder
176455	Glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	C38H2.2	autoimmune disease of blood
176502	Exostosin-2 homolog	rib-2	hereditary multiple exostoses
176557	putative N-acetylgalactosaminyltransferase 9	gly-9
176633	Uracil-DNA glycosylase	ung-1	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
176647	Putative polypeptide N-acetylgalactosaminyltransferase 11	gly-11
176736	Polypeptide N-acetylgalactosaminyltransferase 5	gly-5	colorectal cancer
176760	putative glucosamine-6-phosphate isomerase	T03F6.3
176788	Fructose-bisphosphate aldolase 1	aldo-1	autoimmune disease of the nervous system borna disease hepatocellular carcinoma hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
176874	Dolichol-phosphate mannosyltransferase subunit 1	dpm-1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
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
177033	Invertebrate-type lysozyme 3	ilys-3
177164	Invertebrate-type lysozyme 6	ilys-6
177235	2-oxoglutarate dehydrogenase, mitochondrial;Transketolase-like pyrimidine-binding domain-containing protein	ogdh-1	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
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

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