GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

Genes (1020) Glycoproteins (765) Lectins (34)

Displaying entries **401 - 425** of **1020** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
852063	endopolyphosphatase	PPN1
853618	endo-polygalacturonase	PGU1
850836	endo-1,3(4)-beta-glucanase	ACF2
855804	endo-1,3(4)-beta-glucanase	DSE4
855491	elongin A	ELA1
853870	dynamin-like GTPase VPS1	VPS1
854336	dynamin-like GTPase SEY1	SEY1
851932	double-stranded DNA-dependent ATPase	IRC3
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
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
851462	dolichyl-phosphate-mannose-protein mannosyltransferase PMT1	PMT1
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
855874	dolichyl-phosphate beta-glucosyltransferase	ALG5	congenital disorder of glycosylation type I polycystic kidney disease
856313	dolichyl-phosphate beta-D-mannosyltransferase	DPM1	breast cancer congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
856716	dolichyl-diphosphooligosaccharide-protein glycotransferase	WBP1	congenital disorder of glycosylation Ir
853455	dolichyl-diphosphooligosaccharide--protein glycotransferase subunit OST1	OST1
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
852862	dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3	STT3	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
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
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
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
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
853142	dolichyl-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-dolichol alpha-1,2- glucosyltransferase	DIE2	long QT syndrome 2 nonsyndromic deafness

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