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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 **1 - 25** 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:12858	Huntington's disease	WB:WBGene00018294	Caenorhabditis elegans	179246	atg-18	combinatorial experimental and author inference evidence used in manual assertion	PMID:17172799
DOID:809	cocaine abuse	WB:WBGene00003386	Caenorhabditis elegans	179269	mod-1	mutant phenotype evidence used in manual assertion	PMID:19536276
DOID:14250	Down syndrome	WB:WBGene00010757	Caenorhabditis elegans	259529	pad-2	mutant phenotype evidence used in manual assertion	PMID:15233996
DOID:9970	obesity	WB:WBGene00001650	Caenorhabditis elegans	177850	gon-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:34492009
DOID:9352	type 2 diabetes mellitus	WB:WBGene00001650	Caenorhabditis elegans	177850	gon-1	mutant phenotype evidence used in manual assertion	PMID:26218657
DOID:1289	neurodegenerative disease	WB:WBGene00010775	Caenorhabditis elegans	187297	poml-1	mutant phenotype evidence used in manual assertion	PMID:26941331
DOID:0050659	biotin-responsive basal ganglia disease	WB:WBGene00044738	Caenorhabditis elegans	4363081	folt-3	mutant phenotype evidence used in manual assertion	PMID:17475669
DOID:1184	nephrotic syndrome	WB:WBGene00006365	Caenorhabditis elegans	180555	syg-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:20233749
DOID:1574	alcohol use disorder	WB:WBGene00001172	Caenorhabditis elegans	179412	egl-3	mutant phenotype evidence used in manual assertion	PMID:19535903
DOID:809	cocaine abuse	WB:WBGene00000295	Caenorhabditis elegans	180837	cat-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:22642886
DOID:0060041	autism spectrum disorder	WB:WBGene00003182	Caenorhabditis elegans	172732	mef-2	combinatorial experimental and author inference evidence used in manual assertion	PMID:22859820
DOID:9970	obesity	WB:WBGene00001609	Caenorhabditis elegans	176286	glp-1	mutant phenotype evidence used in manual assertion	PMID:34492009
DOID:1289	neurodegenerative disease	WB:WBGene00004033	Caenorhabditis elegans	181166	pkc-2	sequence orthology evidence used in manual assertion	PMID:28716951
DOID:206	hereditary multiple exostoses	WB:WBGene00004360	Caenorhabditis elegans	178080	rib-1	mutant phenotype evidence used in manual assertion	PMID:17237233
DOID:2962	Cockayne syndrome	WB:WBGene00008403	Caenorhabditis elegans	174474	csa-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:25453470
DOID:9352	type 2 diabetes mellitus	WB:WBGene00004049	Caenorhabditis elegans	266823	parp-1	mutant phenotype evidence used in manual assertion	PMID:29392078
DOID:1574	alcohol use disorder	WB:WBGene00006797	Caenorhabditis elegans	172150	unc-63	combinatorial experimental and author inference evidence used in manual assertion	PMID:25342716
DOID:162	cancer	WB:WBGene00002081	Caenorhabditis elegans	176296	ina-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:21572423
DOID:14452	hypokalemic periodic paralysis	WB:WBGene00000950	Caenorhabditis elegans	181035	deg-1	mutant phenotype evidence used in manual assertion	PMID:8994058
DOID:0080490	mucolipidosis type IV	WB:WBGene00000846	Caenorhabditis elegans	176074	cup-5	mutant phenotype evidence used in manual assertion	PMID:11904372 PMID:16530747 PMID:20540742
DOID:1289	neurodegenerative disease	WB:WBGene00001612	Caenorhabditis elegans	176204	glr-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:31306683
DOID:2843	long QT syndrome	WB:WBGene00006830	Caenorhabditis elegans	175527	unc-103	mutant phenotype evidence used in manual assertion	PMID:19038263
DOID:2978	carbohydrate metabolic disorder	WB:WBGene00001645	Caenorhabditis elegans	179562	gly-20	sequence orthology evidence used in manual assertion	PMID:35586945
DOID:0090145	dopamine beta-hydroxylase deficiency	WB:WBGene00000934	Caenorhabditis elegans	176304	dat-1	mutant phenotype evidence used in manual assertion	PMID:18768815
DOID:9870	galactosemia	WB:WBGene00008132	Caenorhabditis elegans	173171	gale-1	mutant phenotype evidence used in manual assertion	PMID:25298520

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