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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 **151 - 175** 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:10652	Alzheimer's disease	MGI:88059	Mus musculus (house mouse)	11820	App	author statement supported by traceable reference	PMID:10188929 PMID:15147316 PMID:16279840 PMID:24728269 PMID:27109181 PMID:8798542
DOID:10608	celiac disease	HGNC:2505	Homo sapiens (human)	1493	CTLA4	inference by association of genotype from phenotype used in manual assertion	PMID:10189842 PMID:19020530 RGD:7240710
DOID:0060680	pigment dispersion syndrome	MGI:1934765	Mus musculus (house mouse)	93695	Gpnmb	author statement supported by traceable reference	PMID:10192392 PMID:16827931
DOID:2566	corneal dystrophy	HGNC:11530	Homo sapiens (human)	4070	TACSTD2	inference by association of genotype from phenotype used in manual assertion	PMID:10192395
DOID:576	proteinuria	HGNC:2707	Homo sapiens (human)	1636	ACE	inference by association of genotype from phenotype used in manual assertion	PMID:10193250
DOID:5844	myocardial infarction	HGNC:6137	Homo sapiens (human)	3673	ITGA2	inference by association of genotype from phenotype used in manual assertion	PMID:10194421 PMID:16697311
DOID:2352	hemochromatosis	HGNC:4886	Homo sapiens (human)	3077	HFE	inference by association of genotype from phenotype used in manual assertion	PMID:10194428 PMID:12850493 PMID:30651232 PMID:8696333
DOID:5844	myocardial infarction	HGNC:1628	Homo sapiens (human)	929	CD14	inference by association of genotype from phenotype used in manual assertion	PMID:10195920 PMID:14587643
DOID:0050554	X-linked sideroblastic anemia with ataxia	HGNC:48	Homo sapiens (human)	22	ABCB7	inference by association of genotype from phenotype used in manual assertion	PMID:10196363 PMID:11050011 PMID:11843825 RGD:7240710
DOID:1070	primary open angle glaucoma	HGNC:7610	Homo sapiens (human)	4653	MYOC	inference by association of genotype from phenotype used in manual assertion	PMID:10196380 PMID:11595024 PMID:12189160 PMID:12447164 PMID:15483649 PMID:16431959 PMID:17197538 PMID:18334962 PMID:19145250 PMID:19688280 PMID:21655360 PMID:22736945 PMID:22879734 PMID:22933836 PMID:23453510 PMID:9005853 PMID:9535666
DOID:988	mitral valve prolapse	HGNC:12373	Homo sapiens (human)	7253	TSHR	inference by association of genotype from phenotype used in manual assertion	PMID:10199795
DOID:1205	allergic disease	HGNC:333	Homo sapiens (human)	183	AGT	inference by association of genotype from phenotype used in manual assertion	PMID:10200023
DOID:1205	allergic disease	HGNC:2707	Homo sapiens (human)	1636	ACE	inference by association of genotype from phenotype used in manual assertion	PMID:10200023
DOID:6688	autoimmune lymphoproliferative syndrome	HGNC:11920	Homo sapiens (human)	355	FAS	direct assay evidence used in manual assertion	PMID:10200300
DOID:526	human immunodeficiency virus infectious disease	HGNC:11920	Homo sapiens (human)	355	FAS	direct assay evidence used in manual assertion	PMID:10200468
DOID:1588	thrombocytopenia	HGNC:3616	Homo sapiens (human)	2212	FCGR2A	mutant phenotype evidence used in manual assertion	PMID:10201963
DOID:11633	thyroid hormone resistance syndrome	MGI:1276523	Mus musculus (house mouse)	17977	Ncoa1	author statement supported by traceable reference	PMID:10202153
DOID:1205	allergic disease	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:10202362 PMID:10689122 PMID:15853900 PMID:16112029 PMID:20684489
DOID:1205	allergic disease	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:10202362 PMID:15853900 PMID:16112029
DOID:5082	liver cirrhosis	HGNC:4938	Homo sapiens (human)	3113	HLA-DPA1	inference by association of genotype from phenotype used in manual assertion	PMID:10203020
DOID:0050589	inflammatory bowel disease	MGI:104798	Mus musculus (house mouse)	21926	Tnf	author statement supported by traceable reference	PMID:10204494 PMID:18439426 PMID:23977107 PMID:23977323
DOID:7148	rheumatoid arthritis	MGI:104798	Mus musculus (house mouse)	21926	Tnf	author statement supported by traceable reference	PMID:10204494 PMID:26195802 PMID:29618659
DOID:10652	Alzheimer's disease	HGNC:6677	Homo sapiens (human)	4023	LPL	inference by association of genotype from phenotype used in manual assertion	PMID:10206232 PMID:15331147 PMID:16013913 PMID:16965549
DOID:4947	cholangiocarcinoma	HGNC:583	Homo sapiens (human)	324	APC	inference by association of genotype from phenotype used in manual assertion	PMID:10212000
DOID:480	movement disease	HGNC:3023	Homo sapiens (human)	1813	DRD2	inference by association of genotype from phenotype used in manual assertion	PMID:10220438

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