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 ▼
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
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
852362	N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase anchoring subunit ALG14	ALG14	congenital myasthenic syndrome 15
855687	Golgi transport complex subunit COG6	COG6	congenital disorder of glycosylation type IIl
855676	Golgi transport complex subunit COG5	COG5	congenital disorder of glycosylation type IIi
854904	Golgi transport complex subunit COG8	COG8	congenital disorder of glycosylation type IIh
852857	mannosyl-oligosaccharide glucosidase	CWH41	congenital disorder of glycosylation type IIb
856901	Golgi transport complex subunit COG3	COG3	congenital disorder of glycosylation type II
855874	dolichyl-phosphate beta-glucosyltransferase	ALG5	congenital disorder of glycosylation type I polycystic kidney disease
852862	dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3	STT3	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
853732	phosphoglucomutase PGM1	PGM1	congenital disorder of glycosylation It endometrial cancer teratoma
855131	phosphoglucomutase PGM2	PGM2	congenital disorder of glycosylation It endometrial cancer teratoma
856716	dolichyl-diphosphooligosaccharide-protein glycotransferase	WBP1	congenital disorder of glycosylation Ir
855679	alpha-1,2-mannosyltransferase ALG11	ALG11	congenital disorder of glycosylation Ip
852407	chitobiosyldiphosphodolichol beta-1,4 mannosyltransferase	ALG1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
852545	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	ALG7	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
852815	GDP-Man:Man(1)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase	ALG2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
854233	dolichyl-P-Glc:Glc1Man(9)GlcNAc(2)-PP-dolichol alpha-1,3-glucosyltransferase	ALG8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
855764	dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichol alpha-1,6-mannosyltransferase	ALG12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
852196	dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase	ALG3	congenital disorder of glycosylation Id congenital disorder of glycosylation
854163	dolichyl-P-Glc:Man(9)GlcNAc(2)-PP-dolichol alpha-1,3-glucosyltransferase	ALG6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
850499	phosphomannomutase SEC53	SEC53	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congenital disorder of glycosylation
852306	UDP-glucose:hexose-1-phosphate uridylyltransferase	GAL7	classic galactosemia galactosemia
854419	diacylglycerol O-acyltransferase	DGA1	chronic kidney disease dry eye syndrome metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease
852796	O-acyltransferase	GUP1	chondrodysplasia-pseudohermaphroditism syndrome

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