GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

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

Displaying entries **76 - 100** of **362** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
851848	glucan exo-1,3-beta-glucosidase	EXG2
851902	putative dolichyl-phosphate-mannose--protein mannosyltransferase	PMT7
851956	anthranilate phosphoribosyltransferase	TRP4
851974	trifunctional aldehyde reductase/carbonyl reductase (NADPH)/glucose 1-dehydrogenase (NADP(+)) YPR1	YPR1	46,XY sex reversal 8 B-lymphoblastic leukemia/lymphoma T-cell acute lymphoblastic leukemia allergic disease arteriosclerosis breast cancer castration-resistant prostate carcinoma cataract congenital bile acid synthesis defect 2 diabetic neuropathy diabetic retinopathy ductal carcinoma in situ galactosemia hepatocellular carcinoma hyperglycemia hypokalemia leukemia lung adenocarcinoma obesity polycystic ovary syndrome pre-eclampsia prostate cancer stomach cancer type 2 diabetes mellitus
851977	putative chitinase	CTS2	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease cryptococcosis endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia silicosis sinusitis small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
852008	hypoxanthine phosphoribosyltransferase	HPT1
852009	trifunctional uridine nucleosidase/nicotinamide riboside hydrolase/nicotinic acid riboside hydrolase	URH1
852030	Hkr1p	HKR1
852047	phosphatidylinositol N-acetylglucosaminyltransferase GPI19	GPI19	developmental and epileptic encephalopathy 55
852051	adenine phosphoribosyltransferase APT2	APT2	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
852080	Sdc1p	SDC1
852094	alpha-1,2-mannosyltransferase KRE2	KRE2
852128	putative glucokinase	EMI2	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 obesity permanent neonatal diabetes mellitus retinitis pigmentosa steatotic liver disease type 2 diabetes mellitus
852196	dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase	ALG3	congenital disorder of glycosylation Id congenital disorder of glycosylation
852222	protein phosphatase regulator SHP1	SHP1
852261	glycolipid translocation protein	RFT1	cancer congenital disorder of glycosylation In congenital disorder of glycosylation type I
852286	alpha,alpha-trehalase NTH2	NTH2
852289	GPI-anchor transamidase GPI18	GPI18	hyperphosphatasia with impaired intellectual development syndrome 1
852303	alpha-1,2-mannosyltransferase MNN2	MNN2
852306	UDP-glucose:hexose-1-phosphate uridylyltransferase	GAL7	classic galactosemia galactosemia
852307	bifunctional UDP-glucose 4-epimerase/aldose 1-epimerase	GAL10	galactose epimerase deficiency galactosemia thrombocytopenia
852308	galactokinase	GAL1
852310	ADP-ribose 1''-phosphate phosphatase	POA1
852311	chitin synthase CHS3	CHS3
852317	phosphatidate cytidylyltransferase	CDS1	cancer

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