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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source	Last Updated
Alliance of Genome Resources	October 9, 2024

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID ▲	Gene Symbol	Evidence Code Names	References
DOID:14679	VACTERL association	SGD:S000005182	Saccharomyces cerevisiae S288C	855483	KEX2	evidence used in automatic assertion	MGI:6194238
DOID:1508	candidiasis	SGD:S000005174	Saccharomyces cerevisiae S288C	855491	ELA1	evidence used in automatic assertion	MGI:6194238
DOID:0080564	congenital disorder of glycosylation Il	SGD:S000005163	Saccharomyces cerevisiae S288C	855502	ALG9	evidence used in automatic assertion	MGI:6194238
DOID:3312	bipolar disorder	SGD:S000005163	Saccharomyces cerevisiae S288C	855502	ALG9	sequence similarity evidence used in manual assertion	PMID:12030331
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000005163	Saccharomyces cerevisiae S288C	855502	ALG9	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:15148656 PMID:15945070
DOID:5679	retinal disease	SGD:S000005113	Saccharomyces cerevisiae S288C	855552	PSD1	evidence used in automatic assertion	MGI:6194238
DOID:14330	Parkinson's disease	SGD:S000005113	Saccharomyces cerevisiae S288C	855552	PSD1	mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:25201965
DOID:1074	kidney failure	SGD:S000005086	Saccharomyces cerevisiae S288C	855580	MEP2	evidence used in automatic assertion	MGI:6194238
DOID:4500	hypokalemia	SGD:S000005086	Saccharomyces cerevisiae S288C	855580	MEP2	evidence used in automatic assertion	MGI:6194238
DOID:0050758	metabolic acidosis	SGD:S000005086	Saccharomyces cerevisiae S288C	855580	MEP2	evidence used in automatic assertion	MGI:6194238
DOID:14219	renal tubular acidosis	SGD:S000005086	Saccharomyces cerevisiae S288C	855580	MEP2	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:23967154
DOID:0112056	X-linked intellectual disability-short stature-overweight syndrome	SGD:S000005083	Saccharomyces cerevisiae S288C	855583	THO2	evidence used in automatic assertion	MGI:6194238
DOID:3319	lymphangioleiomyomatosis	SGD:S000005069	Saccharomyces cerevisiae S288C	855598	ESBP6	evidence used in automatic assertion	MGI:6194238
DOID:0070214	familial hyperinsulinemic hypoglycemia 7	SGD:S000005069	Saccharomyces cerevisiae S288C	855598	ESBP6	evidence used in automatic assertion	MGI:6194238
DOID:0070353	cataract 47	SGD:S000005069	Saccharomyces cerevisiae S288C	855598	ESBP6	evidence used in automatic assertion	MGI:6194238
DOID:0111840	Van Esch-O'Driscoll syndrome	SGD:S000005046	Saccharomyces cerevisiae S288C	855621	POL1	evidence used in automatic assertion	MGI:6194238
DOID:0111834	X-linked reticulate pigmentary disorder	SGD:S000005046	Saccharomyces cerevisiae S288C	855621	POL1	evidence used in automatic assertion	MGI:6194238
DOID:0070261	congenital disorder of glycosylation type IIi	SGD:S000004996	Saccharomyces cerevisiae S288C	855676	COG5	evidence used in automatic assertion	MGI:6194238
DOID:0080567	congenital disorder of glycosylation Ip	SGD:S000004993	Saccharomyces cerevisiae S288C	855679	ALG11	evidence used in automatic assertion	MGI:6194238
DOID:0070264	congenital disorder of glycosylation type IIl	SGD:S000004986	Saccharomyces cerevisiae S288C	855687	COG6	evidence used in automatic assertion	MGI:6194238
DOID:0050709	early infantile epileptic encephalopathy	SGD:S000004982	Saccharomyces cerevisiae S288C	855691	IDH1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:28058510
DOID:0110409	retinitis pigmentosa 46	SGD:S000004982	Saccharomyces cerevisiae S288C	855691	IDH1	evidence used in automatic assertion	MGI:6194238
DOID:14330	Parkinson's disease	SGD:S000004965	Saccharomyces cerevisiae S288C	855711	ARK1	evidence used in automatic assertion	MGI:6194238
DOID:3070	high grade glioma	SGD:S000004954	Saccharomyces cerevisiae S288C	855723	IDP3	evidence used in automatic assertion	MGI:6194238
DOID:0080005	bone remodeling disease	SGD:S000004954	Saccharomyces cerevisiae S288C	855723	IDP3	evidence used in automatic assertion	MGI:6194238

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