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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:1184	nephrotic syndrome	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:219	colon cancer	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:3021	acute kidney failure	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:10591	pre-eclampsia	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:9256	colorectal cancer	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:0050861	colorectal adenocarcinoma	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:0112298	spondylometaphyseal dysplasia Sedaghatian type	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:0050579	glycogen storage disease XV	SGD:S000001766	Saccharomyces cerevisiae S288C	853932	GLG1	evidence used in automatic assertion	MGI:6194238
DOID:2747	glycogen storage disease	SGD:S000001766	Saccharomyces cerevisiae S288C	853932	GLG1	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:6000	congestive heart failure	SGD:S000005486	Saccharomyces cerevisiae S288C	853994	MDH2	evidence used in automatic assertion	MGI:6194238
DOID:0110853	rhizomelic chondrodysplasia punctata type 3	HGNC:327	Homo sapiens (human)	8540	AGPS	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 RGD:7240710
DOID:2580	rhizomelic chondrodysplasia punctata	HGNC:327	Homo sapiens (human)	8540	AGPS	direct assay evidence used in manual assertion	PMID:9553082
DOID:9266	cystinuria	SGD:S000005517	Saccharomyces cerevisiae S288C	854008	IMA2	evidence used in automatic assertion	MGI:6194238
DOID:0110219	Brugada syndrome 2	SGD:S000005420	Saccharomyces cerevisiae S288C	854095	GPD2	evidence used in automatic assertion	MGI:6194238
DOID:0080411	familial adenomatous polyposis 3	SGD:S000005403	Saccharomyces cerevisiae S288C	854114	NTG2	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:0080555	congenital disorder of glycosylation Ic	SGD:S000005528	Saccharomyces cerevisiae S288C	854163	ALG6	evidence used in automatic assertion	MGI:6194238
DOID:0050770	polycystic liver disease	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:0080560	congenital disorder of glycosylation Ih	SGD:S000005593	Saccharomyces cerevisiae S288C	854233	ALG8	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:0111839	congenital disorder of glycosylation Icc	SGD:S000005611	Saccharomyces cerevisiae S288C	854252	OST3	evidence used in automatic assertion	MGI:6194238

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