GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

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

Displaying entries **51 - 75** of **362** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
853624	L-iditol 2-dehydrogenase SOR1	SOR1	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
851351	L-iditol 2-dehydrogenase SOR2	SOR2	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
850759	D-xylulose reductase XYL2	XYL2	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
850704	S-methyl-5-thioadenosine phosphorylase	MEU1	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
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
850361	citrate (Si)-synthase CIT2	CIT2	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
855732	citrate (Si)-synthase CIT1	CIT1	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
856107	citrate (Si)-synthase CIT3	CIT3	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
850683	Fps1p	FPS1	brain edema
853994	malate dehydrogenase MDH2	MDH2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
853777	malate dehydrogenase MDH1	MDH1	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
851481	malate dehydrogenase MDH3	MDH3	brain ischemia congestive heart failure myocardial infarction
856313	dolichyl-phosphate beta-D-mannosyltransferase	DPM1	breast cancer congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
854768	cytochrome-b5 reductase	CBR1	breast cancer estrogen-receptor negative breast cancer methemoglobinemia
851620	triose-phosphate isomerase TPI1	TPI1	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
856652	phosphoacetylglucosamine mutase PCM1	PCM1	cancer cervical cancer immunodeficiency 23 teratoma
852261	glycolipid translocation protein	RFT1	cancer congenital disorder of glycosylation In congenital disorder of glycosylation type I
853830	UTP glucose-1-phosphate uridylyltransferase	UGP1	cancer developmental and epileptic encephalopathy 83
854320	glycosylphosphatidylinositol-alpha 1,2 mannosyltransferase	SMP3	cancer
856439	2-deoxyglucose-6-phosphatase	DOG2	cancer
852317	phosphatidate cytidylyltransferase	CDS1	cancer
856720	mannose-6-phosphate isomerase PMI40	PMI40	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
852934	sedoheptulose-7-phosphate:D-glyceraldehyde-3-phosphate transaldolase NQM1	NQM1	carbohydrate metabolic disorder
851068	sedoheptulose-7-phosphate:D-glyceraldehyde-3-phosphate transaldolase TAL1	TAL1	carbohydrate metabolic disorder
856289	glycogen phosphorylase	GPH1	cholestasis glycogen storage disease V glycogen storage disease VI glycogen storage disease lactic acidosis

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