GlyCosmos Portal

Saccharomyces cerevisiae S288C

Summary

Taxonomy ID: 559292
PubChem Taxonomy: 559292

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

Displaying entries **301 - 325** of **362** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
853391	Log1p	LOG1
851351	L-iditol 2-dehydrogenase SOR2	SOR2	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
853624	L-iditol 2-dehydrogenase SOR1	SOR1	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
853265	Kre9p	KRE9
854514	Kre5p	KRE5
851511	Knh1p	KNH1
850603	Keg1p	KEG1
850572	Igd1p	IGD1
853295	Ids2p	IDS2
853418	Hsp70 family ATPase KAR2	KAR2	dopamine beta-hydroxylase deficiency high grade glioma inflammatory bowel disease post-traumatic stress disorder rheumatoid arthritis steatotic liver disease transient cerebral ischemia ureteral obstruction visual epilepsy
852030	Hkr1p	HKR1
851807	Gtb1p	GTB1	liver disease polycystic liver disease
854904	Golgi transport complex subunit COG8	COG8	congenital disorder of glycosylation type IIh
852879	Golgi transport complex subunit COG7	COG7
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
856220	Golgi transport complex subunit COG4	COG4	Saul-Wilson syndrome congenital disorder of glycosylation type IIj
856901	Golgi transport complex subunit COG3	COG3	congenital disorder of glycosylation type II
853017	Golgi transport complex subunit COG2	COG2
852649	Golgi transport complex subunit COG1	COG1
855359	Glc8p	GLC8
856781	Gip2p	GIP2	alcohol use disorder hypoglycemia type 2 diabetes mellitus
850777	GPI-anchor transamidase subunit GAA1	GAA1
852289	GPI-anchor transamidase GPI18	GPI18	hyperphosphatasia with impaired intellectual development syndrome 1
852815	GDP-Man:Man(1)GlcNAc(2)-PP-dolichol alpha-1,3-mannosyltransferase	ALG2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14