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 ▲
850962	glycogen (starch) synthase GSY2	GSY2	Lafora disease cardiovascular system disease glycogen storage disease
850569	glycogen (starch) synthase GSY1	GSY1	Lafora disease cardiovascular system disease glycogen storage disease
856870	type 1 serine/threonine-protein phosphatase catalytic subunit GLC7	GLC7	Noonan syndrome-like disorder with loose anagen hair 2 cancer congestive heart failure type 2 diabetes mellitus
852495	glucose-6-phosphate isomerase	PGI1	Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia congenital hemolytic anemia congenital nonspherocytic hemolytic anemia heart disease intellectual disability neuromuscular disease
850370	phosphoglycerate kinase	PGK1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
851013	aconitate hydratase ACO1	ACO1	Parkinson's disease central nervous system disease infantile cerebellar-retinal degeneration neurodegenerative disease optic atrophy 9 optic nerve disease
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
853595	mannosyl-oligosaccharide 1,2-alpha-mannosidase	MNS1	Rafiq syndrome
856220	Golgi transport complex subunit COG4	COG4	Saul-Wilson syndrome congenital disorder of glycosylation type IIj
853608	dolichyl-phosphate-mannose-protein mannosyltransferase	PMT4	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
854499	dolichyl-phosphate-mannose-protein mannosyltransferase PMT3	PMT3	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
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
853113	dolichyl-phosphate-mannose-protein mannosyltransferase PMT6	PMT6	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
854252	dolichyl-diphosphooligosaccharide--protein glycotransferase OST3	OST3	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia autosomal recessive intellectual developmental disorder 7 bacterial infectious disease congenital disorder of glycosylation Icc primary immunodeficiency disease prostate cancer
852546	glutathione peroxidase GPX2	GPX2	acute kidney failure colon cancer colorectal adenocarcinoma colorectal cancer gastric adenocarcinoma nephrotic syndrome pre-eclampsia spondylometaphyseal dysplasia Sedaghatian type
853842	glutathione peroxidase GPX1	GPX1	acute kidney failure colon cancer colorectal adenocarcinoma colorectal cancer gastric adenocarcinoma nephrotic syndrome pre-eclampsia spondylometaphyseal dysplasia Sedaghatian type
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
856294	Rho family GTPase RHO1	RHO1	acute myocardial infarction asthma breast cancer breast carcinoma colorectal cancer fetal alcohol syndrome hypertension melanoma membranous glomerulonephritis multiple sclerosis neurodegenerative disease obesity ovarian carcinoma peroxisomal biogenesis disorder pulmonary hypertension ulcerative colitis urinary bladder cancer
852051	adenine phosphoribosyltransferase APT2	APT2	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
854986	adenine phosphoribosyltransferase APT1	APT1	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
856781	Gip2p	GIP2	alcohol use disorder hypoglycemia type 2 diabetes mellitus
854350	protein phosphatase regulator GAC1	GAC1	alcohol use disorder hypoglycemia type 2 diabetes mellitus
850979	protein phosphatase regulator PIG1	PIG1	alcohol use disorder type 2 diabetes mellitus
855009	lactoylglutathione lyase GLO1	GLO1	autistic disorder diabetic retinopathy end stage renal disease type 2 diabetes mellitus vascular disease
855928	phosphatidylinositol N-acetylglucosaminyltransferase SPT14	SPT14	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria

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