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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 **10026 - 10050** 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:1405	primary angle-closure glaucoma	HGNC:171	Homo sapiens (human)	90	ACVR1	inference by association of genotype from phenotype used in manual assertion	PMID:32641001
DOID:13641	exfoliation syndrome	HGNC:171	Homo sapiens (human)	90	ACVR1	inference by association of genotype from phenotype used in manual assertion	PMID:32641001
DOID:3911	progeria	MGI:1917925	Mus musculus (house mouse)	70675	Vcpip1	author statement supported by traceable reference	PMID:32649882
DOID:3908	lung non-small cell carcinoma	HGNC:777	Homo sapiens (human)	463	ZFHX3	inference by association of genotype from phenotype used in manual assertion	PMID:32653938
DOID:3910	lung adenocarcinoma	HGNC:777	Homo sapiens (human)	463	ZFHX3	inference by association of genotype from phenotype used in manual assertion	PMID:32653938
DOID:0112306	Mahvash Disease	MGI:99572	Mus musculus (house mouse)	14527	Gcgr	author statement supported by traceable reference	PMID:32677665
DOID:0111809	syndromic microphthalmia 2	MGI:1918708	Mus musculus (house mouse)	71458	Bcor	author statement supported by traceable reference	PMID:32692983
DOID:11717	neonatal diabetes mellitus	MGI:96573	Mus musculus (house mouse)	16334	Ins2	author statement supported by traceable reference	PMID:32699230
DOID:6000	congestive heart failure	RGD:3001	Rattus norvegicus (Norway rat)	24536	Lepr	inference by association of genotype from phenotype used in manual assertion	PMID:32710530
DOID:10763	hypertension	RGD:3001	Rattus norvegicus (Norway rat)	24536	Lepr	inference by association of genotype from phenotype used in manual assertion	PMID:32710530
DOID:9351	diabetes mellitus	HGNC:2433	Homo sapiens (human)	1436	CSF1R	direct assay evidence used in manual assertion	PMID:32724427
DOID:10976	membranous glomerulonephritis	HGNC:1037	Homo sapiens (human)	629	CFB	inference by association of genotype from phenotype used in manual assertion	PMID:3272818
DOID:305	carcinoma	FB:FBgn0003731	Drosophila melanogaster (fruit fly)	37455	Egfr	combinatorial experimental and author inference evidence used in manual assertion	PMID:32737065
DOID:4914	esophagus adenocarcinoma	HGNC:4567	Homo sapiens (human)	2886	GRB7	mutant phenotype evidence used in manual assertion	PMID:32737994
DOID:0080600	COVID-19	HGNC:3541	Homo sapiens (human)	2152	F3	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:0080600	COVID-19	HGNC:7	Homo sapiens (human)	2	A2M	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:0080600	COVID-19	HGNC:1325	Homo sapiens (human)	722	C4BPA	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:0080600	COVID-19	HGNC:1328	Homo sapiens (human)	725	C4BPB	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:0080600	COVID-19	HGNC:9075	Homo sapiens (human)	5345	SERPINF2	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:0080600	COVID-19	HGNC:1318	Homo sapiens (human)	718	C3	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:0080600	COVID-19	HGNC:1228	Homo sapiens (human)	710	SERPING1	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:0080600	COVID-19	HGNC:4883	Homo sapiens (human)	3075	CFH	inference by association of genotype from phenotype used in manual assertion	PMID:32747830
DOID:3748	esophagus squamous cell carcinoma	HGNC:6848	Homo sapiens (human)	4214	MAP3K1	inference by association of genotype from phenotype used in manual assertion	PMID:32753933
DOID:2559	opiate dependence	HGNC:4132	Homo sapiens (human)	2587	GALR1	inference by association of genotype from phenotype used in manual assertion	PMID:32757697
DOID:14330	Parkinson's disease	FB:FBgn0250906	Drosophila melanogaster (fruit fly)	33461	Pgk	combinatorial experimental and author inference evidence used in manual assertion	PMID:32758590

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