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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:6000	congestive heart failure	RGD:3876	Rattus norvegicus (Norway rat)	24835	Tnf	evidence used in automatic assertion expression pattern evidence used in manual assertion mutant phenotype evidence used in manual assertion	MGI:6194238 PMID:11668085 PMID:15210453 PMID:28939262
DOID:9884	muscular dystrophy	HGNC:17997	Homo sapiens (human)	79147	FKRP	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11592034
DOID:13141	uveitis	HGNC:11892	Homo sapiens (human)	7124	TNF	direct assay evidence used in manual assertion evidence used in automatic assertion expression pattern evidence used in manual assertion mutant phenotype evidence used in manual assertion	MGI:6194238 PMID:11586057 PMID:1318867 PMID:15209464 PMID:20673052
DOID:10587	Krabbe disease	MGI:95636	Mus musculus (house mouse)	14420	Galc	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:11461188 PMID:20441793 PMID:21389217 PMID:34142127 PMID:7417782 PMID:7437911
DOID:11476	osteoporosis	HGNC:6553	Homo sapiens (human)	3952	LEP	direct assay evidence used in manual assertion evidence used in automatic assertion expression pattern evidence used in manual assertion	MGI:6194238 PMID:11459801 PMID:21376149
DOID:14504	Niemann-Pick disease	MGI:98325	Mus musculus (house mouse)	20597	Smpd1	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:11454988 PMID:12213735 PMID:12594290 PMID:7600574 PMID:7670466 PMID:8706124 PMID:9382882
DOID:0050559	Fukuyama congenital muscular dystrophy	HGNC:3622	Homo sapiens (human)	2218	FKTN	evidence used in automatic assertion expression pattern evidence used in manual assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11445638 RGD:7240710
DOID:0050773	paraganglioma	HGNC:10681	Homo sapiens (human)	6390	SDHB	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11404820 RGD:7240710
DOID:9352	type 2 diabetes mellitus	MGI:104874	Mus musculus (house mouse)	11652	Akt2	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:11387480
DOID:0070255	congenital disorder of glycosylation type IIc	HGNC:20197	Homo sapiens (human)	55343	SLC35C1	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11326280 RGD:7240710
DOID:9970	obesity	HGNC:4923	Homo sapiens (human)	3099	HK2	direct assay evidence used in manual assertion evidence used in automatic assertion	MGI:6194238 PMID:11319725
DOID:1919	Lesch-Nyhan syndrome	MGI:96217	Mus musculus (house mouse)	15452	Hprt1	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:11297820 PMID:7509865
DOID:6000	congestive heart failure	HGNC:288	Homo sapiens (human)	155	ADRB3	evidence used in automatic assertion expression pattern evidence used in manual assertion	MGI:6194238 PMID:11273992
DOID:10325	silicosis	HGNC:11892	Homo sapiens (human)	7124	TNF	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11264025
DOID:10763	hypertension	HGNC:800	Homo sapiens (human)	477	ATP1A2	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11257061
DOID:2842	Jervell-Lange Nielsen syndrome	MGI:108083	Mus musculus (house mouse)	16535	Kcnq1	author statement supported by traceable reference evidence used in automatic assertion	MGI:6194238 PMID:11226272 PMID:15498462 PMID:15891643
DOID:9744	type 1 diabetes mellitus	HGNC:5993	Homo sapiens (human)	3554	IL1R1	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11197691 PMID:8911996
DOID:12802	mucopolysaccharidosis I	HGNC:5391	Homo sapiens (human)	3425	IDUA	direct assay evidence used in manual assertion evidence used in automatic assertion expression pattern evidence used in manual assertion inference by association of genotype from phenotype used in manual assertion mutant phenotype evidence used in manual assertion	MGI:6194238 PMID:11172140 PMID:12948739 PMID:1301196 PMID:1301941 PMID:15126990 PMID:15128896 PMID:15194053 PMID:16435195 PMID:16860035 PMID:17407189 PMID:17606547 PMID:18523448 PMID:21734815 PMID:24100243 PMID:25597593 PMID:27146977 PMID:7951228 PMID:8664897
DOID:0110671	congenital myasthenic syndrome 6	HGNC:1912	Homo sapiens (human)	1103	CHAT	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11172068 RGD:7240710
DOID:783	end stage renal disease	HGNC:6344	Homo sapiens (human)	9365	KL	evidence used in automatic assertion expression pattern evidence used in manual assertion	MGI:6194238 PMID:11162628
DOID:12801	mucopolysaccharidosis III	HGNC:7632	Homo sapiens (human)	4669	NAGLU	direct assay evidence used in manual assertion evidence used in automatic assertion expression pattern evidence used in manual assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11136549 PMID:11668611 PMID:4261742
DOID:3526	cerebral infarction	HGNC:9603	Homo sapiens (human)	5740	PTGIS	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11130769 PMID:28108096 PMID:28478978
DOID:3068	glioblastoma	HGNC:9604	Homo sapiens (human)	5742	PTGS1	evidence used in automatic assertion expression pattern evidence used in manual assertion	MGI:6194238 PMID:11121536
DOID:3068	glioblastoma	HGNC:9605	Homo sapiens (human)	5743	PTGS2	evidence used in automatic assertion expression pattern evidence used in manual assertion	MGI:6194238 PMID:11121536
DOID:0050453	lissencephaly	HGNC:8574	Homo sapiens (human)	5048	PAFAH1B1	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 PMID:11115846

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