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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 **26 - 50** 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:10003	sensorineural hearing loss	ZFIN:ZDB-GENE-040426-1371	Danio rerio (zebrafish)	393385	slc44a4	author statement supported by traceable reference used in manual assertion	PMID:28013291
DOID:83	cataract	ZFIN:ZDB-GENE-040312-2	Danio rerio (zebrafish)	404210	crim1	author statement supported by traceable reference used in manual assertion	PMID:30979021
DOID:10629	microphthalmia	ZFIN:ZDB-GENE-040312-2	Danio rerio (zebrafish)	404210	crim1	author statement supported by traceable reference used in manual assertion	PMID:30979021
DOID:0050431	arrhythmogenic right ventricular cardiomyopathy	ZFIN:ZDB-GENE-031116-55	Danio rerio (zebrafish)	560091	dsc2l	author statement supported by traceable reference used in manual assertion	PMID:33784018
DOID:5419	schizophrenia	ZFIN:ZDB-GENE-030616-135	Danio rerio (zebrafish)	403310	cacna1da	curator inference used in manual assertion	PMID:33057948
DOID:0110726	neuronal ceroid lipofuscinosis 2	ZFIN:ZDB-GENE-030131-6654	Danio rerio (zebrafish)	798347	tpp1	author statement supported by traceable reference used in manual assertion	PMID:23587805
DOID:1682	congenital heart disease	ZFIN:ZDB-GENE-030131-4714	Danio rerio (zebrafish)	553365	gnptab	author statement supported by traceable reference used in manual assertion	PMID:33055423
DOID:0080070	mucolipidosis II alpha/beta	ZFIN:ZDB-GENE-030131-4714	Danio rerio (zebrafish)	553365	gnptab	author statement supported by traceable reference used in manual assertion	PMID:19834066 PMID:22046029 PMID:26404503 PMID:29539424
DOID:0080488	mucolipidosis	ZFIN:ZDB-GENE-030131-4714	Danio rerio (zebrafish)	553365	gnptab	author statement supported by traceable reference used in manual assertion	PMID:36096887
DOID:0081007	RNASET2-deficient cystic leukoencephalopathy	ZFIN:ZDB-GENE-030131-2513	Danio rerio (zebrafish)	791890	rnaset2	author statement supported by traceable reference used in manual assertion	PMID:32212285 PMID:32295832
DOID:305	carcinoma	ZFIN:ZDB-GENE-020123-2	Danio rerio (zebrafish)	170457	s1pr2	author statement supported by traceable reference used in manual assertion	PMID:25621765
DOID:0070343	CSF1R-related brain malformation and osteopetrosis	ZFIN:ZDB-GENE-001205-1	Danio rerio (zebrafish)	64274	csf1ra	author statement supported by traceable reference used in manual assertion	PMID:30982608
DOID:0050659	biotin-responsive basal ganglia disease	WB:WBGene00044738	Caenorhabditis elegans	4363081	folt-3	mutant phenotype evidence used in manual assertion	PMID:17475669
DOID:0050659	biotin-responsive basal ganglia disease	WB:WBGene00044738	Caenorhabditis elegans	4363081	folt-3	sequence alignment evidence used in manual assertion	PMID:17475669
DOID:65	connective tissue disease	WB:WBGene00022816	Caenorhabditis elegans	176076	fbn-1	mutant phenotype evidence used in manual assertion	PMID:25798732
DOID:65	connective tissue disease	WB:WBGene00022816	Caenorhabditis elegans	176076	fbn-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:25798732
DOID:3211	lysosomal storage disease	WB:WBGene00021546	Caenorhabditis elegans	3565323	laat-1	mutant phenotype evidence used in manual assertion	PMID:22822152
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:0060363	glycerol kinase deficiency	WB:WBGene00020007	Caenorhabditis elegans	173747	R11F4.1	sequence orthology evidence used in manual assertion	PMID:10767309
DOID:14330	Parkinson's disease	WB:WBGene00018878	Caenorhabditis elegans	180747	glit-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:29346364
DOID:14330	Parkinson's disease	WB:WBGene00018878	Caenorhabditis elegans	180747	glit-1	mutant phenotype evidence used in manual assertion	PMID:29346364
DOID:12858	Huntington's disease	WB:WBGene00018294	Caenorhabditis elegans	179246	atg-18	mutant phenotype evidence used in manual assertion	PMID:17172799
DOID:12858	Huntington's disease	WB:WBGene00018294	Caenorhabditis elegans	179246	atg-18	combinatorial experimental and author inference evidence used in manual assertion	PMID:17172799
DOID:0090117	thiamine-responsive megaloblastic anemia syndrome	WB:WBGene00018138	Caenorhabditis elegans	178745	folt-2	sequence orthology evidence used in manual assertion	PMID:17475669
DOID:1574	alcohol use disorder	WB:WBGene00016872	Caenorhabditis elegans	183715	dop-4	mutant phenotype evidence used in manual assertion	PMID:24681782

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