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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

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References ▲
DOID:4195	hyperglycemia	RGD:3396	Rattus norvegicus (Norway rat)	25023	Prkcb	direct assay evidence used in manual assertion	PMID:15616014
DOID:987	alopecia	RGD:735015	Rattus norvegicus (Norway rat)	291754	Dsg4	inference by association of genotype from phenotype used in manual assertion	PMID:15617564
DOID:10914	amnestic disorder	RGD:2521	Rattus norvegicus (Norway rat)	29238	Drd3	mutant phenotype evidence used in manual assertion	PMID:15619116
DOID:3393	coronary artery disease	HGNC:7155	Homo sapiens (human)	4312	MMP1	direct assay evidence used in manual assertion	PMID:15619398
DOID:289	endometriosis	MGI:96680	Mus musculus (house mouse)	16653	Kras	author statement supported by traceable reference	PMID:15619626
DOID:2349	arteriosclerosis	HGNC:7155	Homo sapiens (human)	4312	MMP1	direct assay evidence used in manual assertion	PMID:15621056
DOID:0060673	Peters anomaly	HGNC:2597	Homo sapiens (human)	1545	CYP1B1	inference by association of genotype from phenotype used in manual assertion	PMID:15621878
DOID:10534	stomach cancer	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:15622476
DOID:0111541	pigmented paravenous chorioretinal atrophy	HGNC:2343	Homo sapiens (human)	23418	CRB1	inference by association of genotype from phenotype used in manual assertion	PMID:15623792 RGD:7240710
DOID:0090078	hypogonadotropic hypogonadism 7 with or without anosmia	MGI:95790	Mus musculus (house mouse)	14715	Gnrhr	author statement supported by traceable reference	PMID:15625238
DOID:0111532	osteoglophonic dysplasia	HGNC:3688	Homo sapiens (human)	2260	FGFR1	inference by association of genotype from phenotype used in manual assertion	PMID:15625620 RGD:7240710
DOID:0050741	alcohol dependence	HGNC:4087	Homo sapiens (human)	2566	GABRG2	inference by association of genotype from phenotype used in manual assertion	PMID:15630072
DOID:10754	otitis media	MGI:95522	Mus musculus (house mouse)	14182	Fgfr1	author statement supported by traceable reference	PMID:15630379 PMID:25917818
DOID:5844	myocardial infarction	HGNC:11760	Homo sapiens (human)	7035	TFPI	direct assay evidence used in manual assertion	PMID:15630488
DOID:0050700	cardiomyopathy	RGD:71022	Rattus norvegicus (Norway rat)	81008	Itga7	mutant phenotype evidence used in manual assertion	PMID:15632017
DOID:9351	diabetes mellitus	HGNC:11850	Homo sapiens (human)	7099	TLR4	inference by association of genotype from phenotype used in manual assertion	PMID:15632890
DOID:3393	coronary artery disease	HGNC:11850	Homo sapiens (human)	7099	TLR4	inference by association of genotype from phenotype used in manual assertion	PMID:15632890
DOID:11396	pulmonary edema	HGNC:5973	Homo sapiens (human)	3596	IL13	direct assay evidence used in manual assertion	PMID:15635619
DOID:0050742	nicotine dependence	HGNC:12008	Homo sapiens (human)	7166	TPH1	inference by association of genotype from phenotype used in manual assertion	PMID:15635702
DOID:8778	Crohn's disease	HGNC:5344	Homo sapiens (human)	3383	ICAM1	inference by association of genotype from phenotype used in manual assertion	PMID:15638228
DOID:0050589	inflammatory bowel disease	HGNC:5344	Homo sapiens (human)	3383	ICAM1	inference by association of genotype from phenotype used in manual assertion	PMID:15638228
DOID:5844	myocardial infarction	HGNC:2438	Homo sapiens (human)	1440	CSF3	direct assay evidence used in manual assertion	PMID:15639484
DOID:3407	carotid artery disease	HGNC:1628	Homo sapiens (human)	929	CD14	inference by association of genotype from phenotype used in manual assertion	PMID:15640605 PMID:16873708
DOID:418	systemic scleroderma	HGNC:7176	Homo sapiens (human)	4318	MMP9	direct assay evidence used in manual assertion	PMID:15642145
DOID:10763	hypertension	HGNC:1029	Homo sapiens (human)	623	BDKRB1	inference by association of genotype from phenotype used in manual assertion	PMID:15643125

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