GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

Genes (1020) Glycoproteins (765) Lectins (34)

Displaying entries **26 - 50** of **1020** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
852342	uncharacterized protein	YBR053C	familial hyperlipidemia hepatocellular carcinoma stomach cancer
856353	glycerol kinase	GUT1	familial hypercholesterolemia glycerol kinase deficiency
853705	phosphoglycerate mutase GPM1	GPM1	familial erythrocytosis 8 myoglobinuria
851218	bifunctional N-glycosylase/AP lyase NTG1	NTG1	familial adenomatous polyposis 3
854114	bifunctional N-glycosylase/AP lyase NTG2	NTG2	familial adenomatous polyposis 3
850990	dodecenoyl-CoA isomerase	ECI1	epilepsy
855691	isocitrate dehydrogenase (NAD(+)) IDH1	IDH1	early infantile epileptic encephalopathy retinitis pigmentosa 46
854303	isocitrate dehydrogenase (NAD(+)) IDH2	IDH2	early infantile epileptic encephalopathy neuromuscular junction disease retinitis pigmentosa 90
854987	uracil-DNA glycosylase	UNG1	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
853418	Hsp70 family ATPase KAR2	KAR2	dopamine beta-hydroxylase deficiency high grade glioma inflammatory bowel disease post-traumatic stress disorder rheumatoid arthritis steatotic liver disease transient cerebral ischemia ureteral obstruction visual epilepsy
851193	pyruvate kinase CDC19	CDC19	disease of metabolism hyperglycemia hypertension metabolic dysfunction-associated steatotic liver disease
855245	6-phosphofructokinase subunit beta	PFK2	disease of metabolism glycogen storage disease VII glycogen storage disease
853155	6-phosphofructokinase subunit alpha	PFK1	disease of metabolism glycogen storage disease VII glycogen storage disease
852735	putative glycosylphosphatidylinositol-alpha 1,2 mannosyltransferase	GPI10	developmental and epileptic encephalopathy 80 sleeping sickness
852047	phosphatidylinositol N-acetylglucosaminyltransferase GPI19	GPI19	developmental and epileptic encephalopathy 55
852835	N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase catalytic subunit ALG13	ALG13	developmental and epileptic encephalopathy 36
852602	alpha-glucosidase MAL32	MAL32	cystinuria
853214	oligo-1,6-glucosidase IMA5	IMA5	cystinuria
853235	oligo-1,6-glucosidase IMA4	IMA4	cystinuria
854008	oligo-1,6-glucosidase IMA2	IMA2	cystinuria
854635	oligo-1,6-glucosidase IMA3	IMA3	cystinuria
853209	alpha-glucosidase MAL12	MAL12	cystinuria
853204	oligo-1,6-glucosidase IMA1	IMA1	cystinuria
856611	alpha-1,2-mannosidase MNL1	MNL1	cystic fibrosis
850317	glucokinase	GLK1	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young obesity permanent neonatal diabetes mellitus retinitis pigmentosa steatotic liver disease type 2 diabetes mellitus

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