GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

Genes (362) Glycoproteins (891) Lectins (34)

Displaying entries **26 - 50** of **362** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
850759	D-xylulose reductase XYL2	XYL2	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
850770	galactose permease GAL2	GAL2
850777	GPI-anchor transamidase subunit GAA1	GAA1
850825	indolepyruvate decarboxylase 5	PDC5
850836	endo-1,3(4)-beta-glucanase	ACF2
850871	isocitrate dehydrogenase (NADP(+)) IDP2	IDP2	D-2-hydroxyglutaric aciduria 2 D-2-hydroxyglutaric aciduria acute myeloid leukemia autoimmune disease bone remodeling disease cancer esophagus squamous cell carcinoma glioblastoma hepatocellular carcinoma hepatocellular clear cell carcinoma high grade glioma intrahepatic cholangiocarcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma lung squamous cell carcinoma myelodysplastic syndrome status epilepticus stomach cancer
850886	sterol 3-beta-glucosyltransferase	ATG26	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
850906	purine-nucleoside phosphorylase	PNP1	purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder
850910	putative glycosylase	CRR1
850962	glycogen (starch) synthase GSY2	GSY2	Lafora disease cardiovascular system disease glycogen storage disease
850979	protein phosphatase regulator PIG1	PIG1	alcohol use disorder type 2 diabetes mellitus
850990	dodecenoyl-CoA isomerase	ECI1	epilepsy
850992	chitinase	CTS1
851007	glucan 1,3-beta-glucosidase	EXG1
851013	aconitate hydratase ACO1	ACO1	Parkinson's disease central nervous system disease infantile cerebellar-retinal degeneration neurodegenerative disease optic atrophy 9 optic nerve disease
851016	chitin deacetylase CDA1	CDA1
851017	chitin deacetylase CDA2	CDA2
851055	1,3-beta-D-glucan synthase	FKS1
851056	1,3-beta-glucanosyltransferase	GAS2
851059	bifunctional fructose-2,6-bisphosphate 2-phosphatase/6-phosphofructo-2-kinase	YLR345W
851068	sedoheptulose-7-phosphate:D-glyceraldehyde-3-phosphate transaldolase TAL1	TAL1	carbohydrate metabolic disorder
851092	fructose 1,6-bisphosphate 1-phosphatase	FBP1	fructose-1,6-bisphosphatase deficiency
851167	hexokinase	NGK1
851193	pyruvate kinase CDC19	CDC19	disease of metabolism hyperglycemia hypertension metabolic dysfunction-associated steatotic liver disease
851210	dolichyl-phosphate-mannose-protein mannosyltransferase PMT2	PMT2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy

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