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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

Displaying entries **62851 - 62875** of **71927** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID ▲	Species	Gene ID	Gene Symbol	Evidence Code Names	References
DOID:0080208	metabolic dysfunction-associated steatotic liver disease	SGD:S000005435	Saccharomyces cerevisiae S288C	854080	YOL075C	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	SGD:S000005435	Saccharomyces cerevisiae S288C	854080	YOL075C	evidence used in automatic assertion	MGI:6194238
DOID:1168	familial hyperlipidemia	SGD:S000005435	Saccharomyces cerevisiae S288C	854080	YOL075C	evidence used in automatic assertion	MGI:6194238
DOID:0090019	sitosterolemia	SGD:S000005435	Saccharomyces cerevisiae S288C	854080	YOL075C	evidence used in automatic assertion	MGI:6194238
DOID:331	central nervous system disease	SGD:S000005444	Saccharomyces cerevisiae S288C	854070	PHM7	evidence used in automatic assertion	MGI:6194238
DOID:3211	lysosomal storage disease	SGD:S000005452	Saccharomyces cerevisiae S288C	854061	YPQ1	evidence used in automatic assertion	MGI:6194238
DOID:1059	intellectual disability	SGD:S000005479	Saccharomyces cerevisiae S288C	854030	MCH4	evidence used in automatic assertion	MGI:6194238
DOID:0050631	Allan-Herndon-Dudley syndrome	SGD:S000005479	Saccharomyces cerevisiae S288C	854030	MCH4	evidence used in automatic assertion	MGI:6194238
DOID:3748	esophagus squamous cell carcinoma	SGD:S000005479	Saccharomyces cerevisiae S288C	854030	MCH4	evidence used in automatic assertion	MGI:6194238
DOID:0070353	cataract 47	SGD:S000005479	Saccharomyces cerevisiae S288C	854030	MCH4	evidence used in automatic assertion	MGI:6194238
DOID:6000	congestive heart failure	SGD:S000005486	Saccharomyces cerevisiae S288C	853994	MDH2	evidence used in automatic assertion	MGI:6194238
DOID:5844	myocardial infarction	SGD:S000005486	Saccharomyces cerevisiae S288C	853994	MDH2	evidence used in automatic assertion	MGI:6194238
DOID:0080433	developmental and epileptic encephalopathy 51	SGD:S000005486	Saccharomyces cerevisiae S288C	853994	MDH2	evidence used in automatic assertion	MGI:6194238
DOID:2316	brain ischemia	SGD:S000005486	Saccharomyces cerevisiae S288C	853994	MDH2	evidence used in automatic assertion	MGI:6194238
DOID:9266	cystinuria	SGD:S000005517	Saccharomyces cerevisiae S288C	854008	IMA2	evidence used in automatic assertion	MGI:6194238
DOID:0080555	congenital disorder of glycosylation Ic	SGD:S000005528	Saccharomyces cerevisiae S288C	854163	ALG6	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000005528	Saccharomyces cerevisiae S288C	854163	ALG6	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:10359825 PMID:10914684 PMID:10924277
DOID:12858	Huntington's disease	SGD:S000005560	Saccharomyces cerevisiae S288C	854199	AKR2	evidence used in automatic assertion	MGI:6194238
DOID:0111446	progressive myoclonus epilepsy 3	SGD:S000005569	Saccharomyces cerevisiae S288C	854208	WHI2	mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:30295347
DOID:0080560	congenital disorder of glycosylation Ih	SGD:S000005593	Saccharomyces cerevisiae S288C	854233	ALG8	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000005593	Saccharomyces cerevisiae S288C	854233	ALG8	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:15235028
DOID:0080319	X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia	SGD:S000005611	Saccharomyces cerevisiae S288C	854252	OST3	evidence used in automatic assertion	MGI:6194238
DOID:0081183	autosomal recessive intellectual developmental disorder 7	SGD:S000005611	Saccharomyces cerevisiae S288C	854252	OST3	evidence used in automatic assertion	MGI:6194238
DOID:612	primary immunodeficiency disease	SGD:S000005611	Saccharomyces cerevisiae S288C	854252	OST3	evidence used in automatic assertion	MGI:6194238
DOID:10283	prostate cancer	SGD:S000005611	Saccharomyces cerevisiae S288C	854252	OST3	evidence used in automatic assertion	MGI:6194238

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