GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

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

Displaying entries **326 - 350** of **362** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
850990	dodecenoyl-CoA isomerase	ECI1	epilepsy
850979	protein phosphatase regulator PIG1	PIG1	alcohol use disorder type 2 diabetes mellitus
850962	glycogen (starch) synthase GSY2	GSY2	Lafora disease cardiovascular system disease glycogen storage disease
850910	putative glycosylase	CRR1
850906	purine-nucleoside phosphorylase	PNP1	purine nucleoside phosphorylase deficiency purine-pyrimidine metabolic disorder
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
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
850836	endo-1,3(4)-beta-glucanase	ACF2
850825	indolepyruvate decarboxylase 5	PDC5
850777	GPI-anchor transamidase subunit GAA1	GAA1
850770	galactose permease GAL2	GAL2
850759	D-xylulose reductase XYL2	XYL2	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
850746	putative mannosidase MNL2	MNL2
850733	indolepyruvate decarboxylase 1	PDC1
850704	S-methyl-5-thioadenosine phosphorylase	MEU1	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
850683	Fps1p	FPS1	brain edema
850666	glutathione transferase GTT2	GTT2	Alzheimer's disease Parkinson's disease asthma
850633	chaperone ATPase HSP104	HSP104	3-methylglutaconic aciduria type 7a 3-methylglutaconic aciduria type 7b severe congenital neutropenia
850614	hexokinase 1	HXK1	Charcot-Marie-Tooth disease type 4G acute lymphoblastic leukemia anemia colorectal cancer congenital nonspherocytic hemolytic anemia coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes glucose metabolism disease hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 multiple myeloma obesity permanent neonatal diabetes mellitus pulmonary hypertension retinitis pigmentosa sickle cell anemia steatotic liver disease type 2 diabetes mellitus urinary bladder cancer
850608	nicotinate-nucleotide diphosphorylase (carboxylating)	BNA6	Huntington's disease
850603	Keg1p	KEG1
850572	Igd1p	IGD1
850569	glycogen (starch) synthase GSY1	GSY1	Lafora disease cardiovascular system disease glycogen storage disease
850553	type 1 protein phosphatase-activating protein YPI1	YPI1
850519	Bst1p	BST1	holoprosencephaly

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