GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

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

Displaying entries **276 - 300** of **362** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
855335	ATP-dependent RNA helicase HAS1	HAS1
855346	amidophosphoribosyltransferase	ADE4	hepatocellular carcinoma renal cell carcinoma
855352	putative family 17 glucosidase	SCW10
855353	putative 1,3-beta-D-glucan synthase	FKS3
855355	1,3-beta-glucanosyltransferase GAS1	GAS1
855359	Glc8p	GLC8
855368	NADP-dependent alcohol dehydrogenase	ADH6
855373	phosphopyruvate hydratase ERR3	ERR3	Alzheimer's disease Parkinsonism aortic valve stenosis hypertension toxic shock syndrome visual epilepsy
855389	Egt2p	EGT2
855392	phosphatidylinositol-3,5-bisphosphate 5-phosphatase	FIG4	Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease Yunis-Varon syndrome amyotrophic lateral sclerosis type 11 bilateral parasagittal parieto-occipital polymicrogyria neurodegenerative disease
855472	Mpa43p	MPA43
855480	glucose-6-phosphate dehydrogenase	ZWF1	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
855502	dolichyl-P-Man:Man(6)GlcNAc(2)-PP-dolichol alpha-1,2-mannosyltransferase	ALG9	bipolar disorder congenital disorder of glycosylation Il congenital disorder of glycosylation type I
855529	chitin synthase CHS1	CHS1
855530	glutamine amidotransferase subunit DUG3	DUG3
855564	Pga1p	PGA1
855606	malate synthase MLS1	MLS1
855659	putative glucosidase SUN4	SUN4
855676	Golgi transport complex subunit COG5	COG5	congenital disorder of glycosylation type IIi
855679	alpha-1,2-mannosyltransferase ALG11	ALG11	congenital disorder of glycosylation Ip
855687	Golgi transport complex subunit COG6	COG6	congenital disorder of glycosylation type IIl
855690	phosphatidylinositol N-acetylglucosaminyltransferase GPI15	GPI15
855691	isocitrate dehydrogenase (NAD(+)) IDH1	IDH1	early infantile epileptic encephalopathy retinitis pigmentosa 46
855703	putative mannosyltransferase	KTR5
855723	isocitrate dehydrogenase (NADP(+)) IDP3	IDP3	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

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