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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

Displaying entries **1 - 25** of **14279** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID ▼	Gene Symbol	Evidence	References
DOID:0050560	Walker-Warburg syndrome	ZFIN:ZDB-GENE-121001-5	Danio rerio (zebrafish)	101669768	b4gat1	author statement supported by traceable reference used in manual assertion	PMID:23359570
DOID:0050656	pseudo-TORCH syndrome 1	HGNC:8104	Homo sapiens (human)	100506658	OCLN	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:8778	Crohn's disease	HGNC:8104	Homo sapiens (human)	100506658	OCLN	direct assay evidence used in manual assertion	PMID:21748286
DOID:2377	multiple sclerosis	HGNC:1645	Homo sapiens (human)	100133941	CD24	inference by association of genotype from phenotype used in manual assertion	PMID:14657362
DOID:0050565	autosomal recessive nonsyndromic deafness	HGNC:33914	Homo sapiens (human)	100127206	MINAR2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050659	biotin-responsive basal ganglia disease	WB:WBGene00044738	Caenorhabditis elegans	4363081	folt-3	sequence alignment evidence used in manual assertion	PMID:17475669
DOID:0050659	biotin-responsive basal ganglia disease	WB:WBGene00044738	Caenorhabditis elegans	4363081	folt-3	mutant phenotype evidence used in manual assertion	PMID:17475669
DOID:11726	Emery-Dreifuss muscular dystrophy	FB:FBgn0261836	Drosophila melanogaster (fruit fly)	3771968	Msp300	combinatorial experimental and author inference evidence used in manual assertion	PMID:26008743 PMID:38757366
DOID:8466	retinal degeneration	FB:FBgn0031414	Drosophila melanogaster (fruit fly)	3771890	eys	combinatorial experimental and author inference evidence used in manual assertion	PMID:24705015
DOID:3211	lysosomal storage disease	WB:WBGene00021546	Caenorhabditis elegans	3565323	laat-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:22822152
DOID:3211	lysosomal storage disease	WB:WBGene00021546	Caenorhabditis elegans	3565323	laat-1	mutant phenotype evidence used in manual assertion	PMID:22822152
DOID:10283	prostate cancer	SGD:S000000966	Saccharomyces cerevisiae S288C	856911	CHD1	mutant phenotype evidence used in manual assertion	PMID:31222142
DOID:10283	prostate cancer	SGD:S000000966	Saccharomyces cerevisiae S288C	856911	CHD1	sequence similarity evidence used in manual assertion	PMID:31222142
DOID:162	cancer	SGD:S000000935	Saccharomyces cerevisiae S288C	856870	GLC7	sequence similarity evidence used in manual assertion	PMID:26354769
DOID:162	cancer	SGD:S000000935	Saccharomyces cerevisiae S288C	856870	GLC7	genetic interaction evidence used in manual assertion	PMID:26354769
DOID:0050477	Liddle syndrome	SGD:S000000927	Saccharomyces cerevisiae S288C	856862	RSP5	genetic interaction evidence used in manual assertion	PMID:12684839
DOID:0050477	Liddle syndrome	SGD:S000000927	Saccharomyces cerevisiae S288C	856862	RSP5	sequence similarity evidence used in manual assertion	PMID:12684839
DOID:2750	glycogen storage disease IV	SGD:S000000737	Saccharomyces cerevisiae S288C	856705	GLC3	sequence similarity evidence used in manual assertion	PMID:8463281
DOID:2750	glycogen storage disease IV	SGD:S000000737	Saccharomyces cerevisiae S288C	856705	GLC3	genetic interaction evidence used in manual assertion	PMID:8463281
DOID:162	cancer	SGD:S000000784	Saccharomyces cerevisiae S288C	856652	PCM1	sequence similarity evidence used in manual assertion	PMID:26354769
DOID:162	cancer	SGD:S000000784	Saccharomyces cerevisiae S288C	856652	PCM1	genetic interaction evidence used in manual assertion	PMID:26354769
DOID:1485	cystic fibrosis	SGD:S000001247	Saccharomyces cerevisiae S288C	856611	MNL1	sequence similarity evidence used in manual assertion	PMID:15215312
DOID:1485	cystic fibrosis	SGD:S000001247	Saccharomyces cerevisiae S288C	856611	MNL1	genetic interaction evidence used in manual assertion	PMID:15215312
DOID:0050873	follicular lymphoma	SGD:S000001143	Saccharomyces cerevisiae S288C	856501	BIG1	mutant phenotype evidence used in manual assertion	PMID:39259764
DOID:0050873	follicular lymphoma	SGD:S000001143	Saccharomyces cerevisiae S288C	856501	BIG1	sequence similarity evidence used in manual assertion	PMID:39259764

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