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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:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2	SGD:S000006096	Saccharomyces cerevisiae S288C	855928	SPT14	evidence used in automatic assertion	MGI:6194238
DOID:0060713	autosomal recessive congenital ichthyosis 4B	SGD:S000006096	Saccharomyces cerevisiae S288C	855928	SPT14	evidence used in automatic assertion	MGI:6194238
DOID:10579	leukodystrophy	SGD:S000006008	Saccharomyces cerevisiae S288C	856018	YDC1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:26792856
DOID:684	hepatocellular carcinoma	SGD:S000006008	Saccharomyces cerevisiae S288C	856018	YDC1	evidence used in automatic assertion	MGI:6194238
DOID:0080547	metabolic dysfunction-associated steatohepatitis	SGD:S000006008	Saccharomyces cerevisiae S288C	856018	YDC1	evidence used in automatic assertion	MGI:6194238
DOID:0081223	glycosylphosphatidylinositol biosynthesis defect 16	SGD:S000005997	Saccharomyces cerevisiae S288C	856029	GPI2	evidence used in automatic assertion	MGI:6194238
DOID:10652	Alzheimer's disease	SGD:S000005920	Saccharomyces cerevisiae S288C	854575	ERR1	evidence used in automatic assertion	MGI:6194238
DOID:1712	aortic valve stenosis	SGD:S000005920	Saccharomyces cerevisiae S288C	854575	ERR1	evidence used in automatic assertion	MGI:6194238
DOID:11832	visual epilepsy	SGD:S000005920	Saccharomyces cerevisiae S288C	854575	ERR1	evidence used in automatic assertion	MGI:6194238
DOID:14115	toxic shock syndrome	SGD:S000005920	Saccharomyces cerevisiae S288C	854575	ERR1	evidence used in automatic assertion	MGI:6194238
DOID:10763	hypertension	SGD:S000005920	Saccharomyces cerevisiae S288C	854575	ERR1	evidence used in automatic assertion	MGI:6194238
DOID:0080855	Parkinsonism	SGD:S000005920	Saccharomyces cerevisiae S288C	854575	ERR1	evidence used in automatic assertion	MGI:6194238
DOID:2861	congenital nonspherocytic hemolytic anemia	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:9352	type 2 diabetes mellitus	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:0014667	disease of metabolism	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:0111077	pyruvate kinase deficiency of red cells	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:0080208	metabolic dysfunction-associated steatotic liver disease	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:12365	malaria	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:1926	Gaucher's disease	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:4195	hyperglycemia	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:10763	hypertension	SGD:S000005874	Saccharomyces cerevisiae S288C	854529	PYK2	evidence used in automatic assertion	MGI:6194238
DOID:0112374	muscular dystrophy-dystroglycanopathy	SGD:S000005848	Saccharomyces cerevisiae S288C	854499	PMT3	evidence used in automatic assertion	MGI:6194238
DOID:0050453	lissencephaly	SGD:S000005848	Saccharomyces cerevisiae S288C	854499	PMT3	evidence used in automatic assertion	MGI:6194238
DOID:0110298	autosomal recessive limb-girdle muscular dystrophy type 2N	SGD:S000005848	Saccharomyces cerevisiae S288C	854499	PMT3	evidence used in automatic assertion	MGI:6194238
DOID:9884	muscular dystrophy	SGD:S000005848	Saccharomyces cerevisiae S288C	854499	PMT3	evidence used in automatic assertion	MGI:6194238

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