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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:1909	melanoma	SGD:S000002779	Saccharomyces cerevisiae S288C	851977	CTS2	evidence used in automatic assertion	MGI:6194238
DOID:0080283	developmental and epileptic encephalopathy 55	SGD:S000002845	Saccharomyces cerevisiae S288C	852047	GPI19	evidence used in automatic assertion	MGI:6194238
DOID:0060350	adenine phosphoribosyltransferase deficiency	SGD:S000002849	Saccharomyces cerevisiae S288C	852051	APT2	evidence used in automatic assertion	MGI:6194238
DOID:684	hepatocellular carcinoma	SGD:S000002849	Saccharomyces cerevisiae S288C	852051	APT2	evidence used in automatic assertion	MGI:6194238
DOID:9993	hypoglycemia	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:0070216	familial hyperinsulinemic hypoglycemia 3	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:11714	gestational diabetes	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:9351	diabetes mellitus	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:0111100	maturity-onset diabetes of the young type 2	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:3393	coronary artery disease	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:10763	hypertension	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:9352	type 2 diabetes mellitus	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:13317	hyperinsulinemic hypoglycemia	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:2018	hyperinsulinism	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:4194	glucose metabolism disease	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:0060639	permanent neonatal diabetes mellitus	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:9452	steatotic liver disease	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:10584	retinitis pigmentosa	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:0080556	congenital disorder of glycosylation Id	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:23038983
DOID:5212	congenital disorder of glycosylation	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:10581255
DOID:0080566	congenital disorder of glycosylation In	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:18313027
DOID:162	cancer	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:26354769
DOID:0070433	hyperphosphatasia with impaired intellectual development syndrome 1	SGD:S000000208	Saccharomyces cerevisiae S288C	852289	GPI18	evidence used in automatic assertion	MGI:6194238

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