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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 **501 - 525** 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:0050742	nicotine dependence	HGNC:6000	Homo sapiens (human)	3557	IL1RN	direct assay evidence used in manual assertion	PMID:10792346
DOID:12894	Sjogren's syndrome	MGI:2676278	Mus musculus (house mouse)	239611	Muc19	author statement supported by traceable reference	PMID:10793067 PMID:15593201 PMID:25447050 PMID:8077681
DOID:9870	galactosemia	SGD:S000000222	Saccharomyces cerevisiae S288C	852306	GAL7	sequence similarity evidence used in manual assertion	PMID:10799308 PMID:24077966 PMID:28213126 PMID:38986816 PMID:8794735
DOID:9870	galactosemia	SGD:S000000222	Saccharomyces cerevisiae S288C	852306	GAL7	genetic interaction evidence used in manual assertion	PMID:10799308
DOID:14504	Niemann-Pick disease	WB:WBGene00003561	Caenorhabditis elegans	180719	ncr-1	mutant phenotype evidence used in manual assertion	PMID:10801441 PMID:15509773
DOID:14504	Niemann-Pick disease	WB:WBGene00003562	Caenorhabditis elegans	176165	ncr-2	mutant phenotype evidence used in manual assertion	PMID:10801441 PMID:15509773
DOID:14504	Niemann-Pick disease	WB:WBGene00003561	Caenorhabditis elegans	180719	ncr-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:10801441 PMID:15509773
DOID:14504	Niemann-Pick disease	WB:WBGene00003562	Caenorhabditis elegans	176165	ncr-2	combinatorial experimental and author inference evidence used in manual assertion	PMID:10801441 PMID:15509773
DOID:2352	hemochromatosis	HGNC:11762	Homo sapiens (human)	7036	TFR2	inference by association of genotype from phenotype used in manual assertion	PMID:10802645
DOID:13832	patent ductus arteriosus	HGNC:11743	Homo sapiens (human)	7021	TFAP2B	inference by association of genotype from phenotype used in manual assertion	PMID:10802654 RGD:7240710
DOID:11342	arcus senilis	HGNC:6309	Homo sapiens (human)	11081	KERA	inference by association of genotype from phenotype used in manual assertion	PMID:10802664
DOID:2566	corneal dystrophy	HGNC:6309	Homo sapiens (human)	11081	KERA	inference by association of genotype from phenotype used in manual assertion	PMID:10802664
DOID:10808	gastric ulcer	RGD:3434	Rattus norvegicus (Norway rat)	25637	Ptger1	mutant phenotype evidence used in manual assertion	PMID:10807413
DOID:2921	glomerulonephritis	RGD:2238	Rattus norvegicus (Norway rat)	24237	C6	inference by association of genotype from phenotype used in manual assertion	PMID:10807586
DOID:3393	coronary artery disease	HGNC:7158	Homo sapiens (human)	4321	MMP12	inference by association of genotype from phenotype used in manual assertion	PMID:10807873
DOID:0060193	amyotrophic lateral sclerosis type 1	HGNC:11179	Homo sapiens (human)	6647	SOD1	inference by association of genotype from phenotype used in manual assertion	PMID:10809943 PMID:20184521 PMID:8446170 PMID:8815157 RGD:7240710
DOID:0050782	Zollinger-Ellison syndrome	HGNC:3229	Homo sapiens (human)	1950	EGF	direct assay evidence used in manual assertion	PMID:10811321
DOID:3393	coronary artery disease	HGNC:11181	Homo sapiens (human)	6649	SOD3	direct assay evidence used in manual assertion	PMID:10811593
DOID:5200	urinary tract obstruction	MGI:109249	Mus musculus (house mouse)	11504	Adamts1	author statement supported by traceable reference	PMID:10811842
DOID:6406	double outlet right ventricle	MGI:1101357	Mus musculus (house mouse)	230857	Ece1	author statement supported by traceable reference	PMID:10811845
DOID:3883	Lynch syndrome	HGNC:6770	Homo sapiens (human)	4089	SMAD4	inference by association of genotype from phenotype used in manual assertion	PMID:10819637
DOID:0060850	annular pancreas	MGI:96533	Mus musculus (house mouse)	16147	Ihh	author statement supported by traceable reference	PMID:10821773
DOID:10487	Hirschsprung's disease	MGI:96533	Mus musculus (house mouse)	16147	Ihh	author statement supported by traceable reference	PMID:10821773
DOID:62	aortic valve disease	MGI:97362	Mus musculus (house mouse)	18127	Nos3	author statement supported by traceable reference	PMID:10821808
DOID:10247	pleurisy	HGNC:5977	Homo sapiens (human)	3600	IL15	direct assay evidence used in manual assertion	PMID:10823416

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