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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	January 28, 2025

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Disease ID	Disease Name	Alliance of Genome Resources ID ▲	Species	Gene ID	Gene Symbol	Evidence	References
DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome	SGD:S000003045	Saccharomyces cerevisiae S288C	852803	HNM1	sequence similarity evidence used in manual assertion	PMID:38302740
DOID:0111666	proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome	SGD:S000003045	Saccharomyces cerevisiae S288C	852803	HNM1	genetic interaction evidence used in manual assertion	PMID:38302740
DOID:9119	acute myeloid leukemia	SGD:S000003060	Saccharomyces cerevisiae S288C	852788	NUP145	mutant phenotype evidence used in manual assertion	PMID:29034209
DOID:9119	acute myeloid leukemia	SGD:S000003060	Saccharomyces cerevisiae S288C	852788	NUP145	sequence similarity evidence used in manual assertion	PMID:29034209
DOID:10112	sleeping sickness	SGD:S000003110	Saccharomyces cerevisiae S288C	852735	GPI10	sequence similarity evidence used in manual assertion	PMID:10954751
DOID:10112	sleeping sickness	SGD:S000003110	Saccharomyces cerevisiae S288C	852735	GPI10	genetic interaction evidence used in manual assertion	PMID:10954751
DOID:0060868	leukoencephalopathy with vanishing white matter	SGD:S000003315	Saccharomyces cerevisiae S288C	852974	GCD2	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:14330	Parkinson's disease	SGD:S000003394	Saccharomyces cerevisiae S288C	853071	TIF4631	mutant phenotype evidence used in manual assertion	PMID:25533483
DOID:14330	Parkinson's disease	SGD:S000003394	Saccharomyces cerevisiae S288C	853071	TIF4631	sequence similarity evidence used in manual assertion	PMID:25533483
DOID:2747	glycogen storage disease	SGD:S000003472	Saccharomyces cerevisiae S288C	853155	PFK1	sequence similarity evidence used in manual assertion	PMID:7825568
DOID:2747	glycogen storage disease	SGD:S000003472	Saccharomyces cerevisiae S288C	853155	PFK1	genetic interaction evidence used in manual assertion	PMID:7825568
DOID:1485	cystic fibrosis	SGD:S000003513	Saccharomyces cerevisiae S288C	853198	YOR1	sequence similarity evidence used in manual assertion	PMID:24876383 PMID:29053845
DOID:1485	cystic fibrosis	SGD:S000003513	Saccharomyces cerevisiae S288C	853198	YOR1	mutant phenotype evidence used in manual assertion	PMID:24876383 PMID:29053845
DOID:162	cancer	SGD:S000003899	Saccharomyces cerevisiae S288C	853603	IML1	sequence similarity evidence used in manual assertion	PMID:23716719
DOID:162	cancer	SGD:S000003899	Saccharomyces cerevisiae S288C	853603	IML1	genetic interaction evidence used in manual assertion	PMID:23716719
DOID:0050560	Walker-Warburg syndrome	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	sequence similarity evidence used in manual assertion	PMID:27358400
DOID:0050560	Walker-Warburg syndrome	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	mutant phenotype evidence used in manual assertion	PMID:27358400
DOID:3070	high grade glioma	SGD:S000004164	Saccharomyces cerevisiae S288C	850871	IDP2	mutant phenotype evidence used in manual assertion	PMID:27427385
DOID:3070	high grade glioma	SGD:S000004164	Saccharomyces cerevisiae S288C	850871	IDP2	sequence similarity evidence used in manual assertion	PMID:27427385
DOID:0080417	developmental and epileptic encephalopathy 38	SGD:S000004232	Saccharomyces cerevisiae S288C	850943	ARV1	mutant phenotype evidence used in manual assertion	PMID:32449190 PMID:32462292
DOID:9455	lipid storage disease	SGD:S000004232	Saccharomyces cerevisiae S288C	850943	ARV1	genetic interaction evidence used in manual assertion	PMID:24273168
DOID:0080417	developmental and epileptic encephalopathy 38	SGD:S000004232	Saccharomyces cerevisiae S288C	850943	ARV1	sequence similarity evidence used in manual assertion	PMID:27270415 PMID:32165008 PMID:32449190 PMID:32462292
DOID:0080417	developmental and epileptic encephalopathy 38	SGD:S000004232	Saccharomyces cerevisiae S288C	850943	ARV1	genetic interaction evidence used in manual assertion	PMID:27270415
DOID:9455	lipid storage disease	SGD:S000004232	Saccharomyces cerevisiae S288C	850943	ARV1	sequence similarity evidence used in manual assertion	PMID:24273168
DOID:1289	neurodegenerative disease	SGD:S000004295	Saccharomyces cerevisiae S288C	851013	ACO1	genetic interaction evidence used in manual assertion	PMID:25351951

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