GlyCosmos Portal

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
851308	uncharacterized protein	YDL218W
851304	Fmp45p	FMP45
851303	Hbt1p	HBT1
851302	Whi4p	WHI4
851299	acid phosphatase PHO11	PHO11
851295	uncharacterized protein	YAR066W
851289	flocculin FLO1	FLO1
851267	tRNA splicing endonuclease subunit SEN34	SEN34
851263	FG-nucleoporin NUP60	NUP60
851246	flavin adenine dinucleotide transporter FLC2	FLC2
851241	calnexin	CNE1
851240	Ecm1p	ECM1
851239	(R,R)-butanediol dehydrogenase	BDH1
851238	putative dehydrogenase BDH2	BDH2
851236	flocculin FLO9	FLO9
851218	bifunctional N-glycosylase/AP lyase NTG1	NTG1	familial adenomatous polyposis 3
851216	serine/threonine protein kinase PSK1	PSK1
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
851193	pyruvate kinase CDC19	CDC19	disease of metabolism hyperglycemia hypertension metabolic dysfunction-associated steatotic liver disease
851180	Nbp1p	NBP1
851171	hydroxymethylglutaryl-CoA reductase (NADPH) HMG2	HMG2
851167	hexokinase	NGK1
851163	chromatin-silencing protein SIR3	SIR3
851132	Pun1p	PUN1
851131	Ina1p	INA1