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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:13166	allergic bronchopulmonary aspergillosis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:11132	prostatic hypertrophy	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:13406	pulmonary sarcoidosis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:0110861	autosomal recessive polycystic kidney disease	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:4988	alcoholic pancreatitis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:3083	chronic obstructive pulmonary disease	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:10652	Alzheimer's disease	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:10808	gastric ulcer	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:0111862	congenital bilateral absence of vas deferens	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:10211	cholelithiasis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:1793	pancreatic cancer	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:1724	duodenal ulcer	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:13316	exocrine pancreatic insufficiency	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:13258	typhoid fever	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:9563	bronchiectasis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:5733	salpingitis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:0050127	sinusitis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:0060643	primary sclerosing cholangitis	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:9351	diabetes mellitus	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:693	dental enamel hypoplasia	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:0111864	autosomal recessive congenital bilateral absence of vas deferens	SGD:S000001811	Saccharomyces cerevisiae S288C	853978	NFT1	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000001849	Saccharomyces cerevisiae S288C	850499	SEC53	evidence used in automatic assertion	MGI:6194238
DOID:5212	congenital disorder of glycosylation	SGD:S000001849	Saccharomyces cerevisiae S288C	850499	SEC53	evidence used in automatic assertion	MGI:6194238
DOID:0080552	congenital disorder of glycosylation Ia	SGD:S000001849	Saccharomyces cerevisiae S288C	850499	SEC53	evidence used in automatic assertion genetic interaction evidence used in manual assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:30530630 PMID:36214454
DOID:0111403	mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations	SGD:S000001861	Saccharomyces cerevisiae S288C	850511	RIM15	evidence used in automatic assertion	MGI:6194238

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