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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	July 29, 2024

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID ▲	Gene Symbol	Evidence Code Names	References
DOID:9352	type 2 diabetes mellitus	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:4194	glucose metabolism disease	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:3393	coronary artery disease	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:0060639	permanent neonatal diabetes mellitus	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:9538	multiple myeloma	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:13317	hyperinsulinemic hypoglycemia	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:9351	diabetes mellitus	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:0110196	Charcot-Marie-Tooth disease type 4G	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:2355	anemia	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:0111100	maturity-onset diabetes of the young type 2	SGD:S000003222	Saccharomyces cerevisiae S288C	852639	HXK2	evidence used in automatic assertion	MGI:6194238
DOID:0050561	Lennox-Gastaut syndrome	HGNC:2851	Homo sapiens (human)	8527	DGKD	evidence used in automatic assertion	MGI:6194238
DOID:10112	sleeping sickness	SGD:S000003110	Saccharomyces cerevisiae S288C	852735	GPI10	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:10954751
DOID:0112216	developmental and epileptic encephalopathy 80	SGD:S000003110	Saccharomyces cerevisiae S288C	852735	GPI10	evidence used in automatic assertion	MGI:6194238
DOID:0060644	chondrodysplasia-pseudohermaphroditism syndrome	SGD:S000003052	Saccharomyces cerevisiae S288C	852796	GUP1	evidence used in automatic assertion	MGI:6194238
DOID:0080561	congenital disorder of glycosylation Ii	SGD:S000003033	Saccharomyces cerevisiae S288C	852815	ALG2	evidence used in automatic assertion	MGI:6194238
DOID:0110669	congenital myasthenic syndrome 14	SGD:S000003033	Saccharomyces cerevisiae S288C	852815	ALG2	evidence used in automatic assertion	MGI:6194238
DOID:3651	pyruvate carboxylase deficiency disease	SGD:S000003030	Saccharomyces cerevisiae S288C	852818	PYC1	evidence used in automatic assertion	MGI:6194238
DOID:0080470	developmental and epileptic encephalopathy 36	SGD:S000003015	Saccharomyces cerevisiae S288C	852835	ALG13	evidence used in automatic assertion	MGI:6194238
DOID:0070254	congenital disorder of glycosylation type IIb	SGD:S000002995	Saccharomyces cerevisiae S288C	852857	CWH41	evidence used in automatic assertion	MGI:6194238
DOID:0080572	congenital disorder of glycosylation Iw	SGD:S000002990	Saccharomyces cerevisiae S288C	852862	STT3	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:34653363
DOID:0080573	congenital disorder of glycosylation Ix	SGD:S000002990	Saccharomyces cerevisiae S288C	852862	STT3	evidence used in automatic assertion	MGI:6194238
DOID:10763	hypertension	HGNC:2645	Homo sapiens (human)	8529	CYP4F2	evidence used in automatic assertion	MGI:6194238
DOID:2978	carbohydrate metabolic disorder	SGD:S000003275	Saccharomyces cerevisiae S288C	852934	NQM1	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	SGD:S000003424	Saccharomyces cerevisiae S288C	853106	TDH3	evidence used in automatic assertion	MGI:6194238

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