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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

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References ▲
DOID:11984	hypertrophic cardiomyopathy	HGNC:6501	Homo sapiens (human)	3920	LAMP2	inference by association of genotype from phenotype used in manual assertion	PMID:15673802 PMID:16144992
DOID:13375	temporal arteritis	HGNC:5438	Homo sapiens (human)	3458	IFNG	inference by association of genotype from phenotype used in manual assertion	PMID:15675129
DOID:14499	Fabry disease	WB:WBGene00011095	Caenorhabditis elegans	179660	gana-1	direct assay evidence used in manual assertion	PMID:15676072
DOID:14499	Fabry disease	WB:WBGene00011095	Caenorhabditis elegans	179660	gana-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:15676072
DOID:1070	primary open angle glaucoma	HGNC:30696	Homo sapiens (human)	134430	WDR36	inference by association of genotype from phenotype used in manual assertion	PMID:15677485 PMID:16723468
DOID:3525	middle cerebral artery infarction	RGD:3035	Rattus norvegicus (Norway rat)	29409	Mag	mutant phenotype evidence used in manual assertion	PMID:15678116
DOID:10808	gastric ulcer	RGD:620630	Rattus norvegicus (Norway rat)	85268	Hrh3	direct assay evidence used in manual assertion	PMID:15680274
DOID:9352	type 2 diabetes mellitus	HGNC:5960	Homo sapiens (human)	3551	IKBKB	direct assay evidence used in manual assertion	PMID:15685173
DOID:0050766	choreaacanthocytosis	MGI:2444304	Mus musculus (house mouse)	271564	Vps13a	author statement supported by traceable reference	PMID:15686477
DOID:3322	GM1 gangliosidosis	MGI:88151	Mus musculus (house mouse)	12091	Glb1	author statement supported by traceable reference	PMID:15687347 PMID:9063740 PMID:9071485 PMID:9337086
DOID:8584	Burkitt lymphoma	MGI:97250	Mus musculus (house mouse)	17869	Myc	author statement supported by traceable reference	PMID:15687498 PMID:22081075 PMID:3906410
DOID:1793	pancreatic cancer	HGNC:1571	Homo sapiens (human)	887	CCKBR	mutant phenotype evidence used in manual assertion	PMID:15688412
DOID:2154	nephroblastoma	HGNC:1101	Homo sapiens (human)	675	BRCA2	inference by association of genotype from phenotype used in manual assertion	PMID:15689453 RGD:7240710
DOID:9352	type 2 diabetes mellitus	HGNC:6081	Homo sapiens (human)	3630	INS	inference by association of genotype from phenotype used in manual assertion	PMID:1569197
DOID:9538	multiple myeloma	HGNC:11913	Homo sapiens (human)	608	TNFRSF17	direct assay evidence used in manual assertion	PMID:15692072
DOID:0080162	lupus nephritis	HGNC:11935	Homo sapiens (human)	959	CD40LG	direct assay evidence used in manual assertion	PMID:15693003
DOID:11723	Duchenne muscular dystrophy	MGI:94909	Mus musculus (house mouse)	13405	Dmd	author statement supported by traceable reference	PMID:15694376 PMID:16857961 PMID:19535499 PMID:20304955 PMID:21893021 PMID:26365037 PMID:26566673 PMID:29187645 PMID:30854433 PMID:31028078 PMID:6583703 PMID:7843915 PMID:9299538 PMID:9626497
DOID:10591	pre-eclampsia	HGNC:11920	Homo sapiens (human)	355	FAS	inference by association of genotype from phenotype used in manual assertion	PMID:15695771 PMID:30066360
DOID:2841	asthma	HGNC:2766	Homo sapiens (human)	1672	DEFB1	inference by association of genotype from phenotype used in manual assertion	PMID:15696078 PMID:16435024
DOID:3070	high grade glioma	HGNC:16421	Homo sapiens (human)	55553	SOX6	direct assay evidence used in manual assertion	PMID:15696967
DOID:0080855	Parkinsonism	RGD:2379	Rattus norvegicus (Norway rat)	24267	Comt	mutant phenotype evidence used in manual assertion	PMID:15698633
DOID:11984	hypertrophic cardiomyopathy	HGNC:11947	Homo sapiens (human)	7137	TNNI3	inference by association of genotype from phenotype used in manual assertion	PMID:15698845
DOID:9744	type 1 diabetes mellitus	HGNC:11848	Homo sapiens (human)	7097	TLR2	inference by association of genotype from phenotype used in manual assertion	PMID:15699513 PMID:19148143
DOID:7148	rheumatoid arthritis	HGNC:11784	Homo sapiens (human)	7056	THBD	direct assay evidence used in manual assertion	PMID:15700117
DOID:9352	type 2 diabetes mellitus	HGNC:4195	Homo sapiens (human)	2645	GCK	inference by association of genotype from phenotype used in manual assertion	PMID:1570017 PMID:8325445 RGD:7240710

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