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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 **376 - 400** 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:0050855	renal fibrosis	RGD:2866	Rattus norvegicus (Norway rat)	25712	Ifng	direct assay evidence used in manual assertion	PMID:10594787
DOID:552	pneumonia	RGD:3644	Rattus norvegicus (Norway rat)	29397	Ccl11	mutant phenotype evidence used in manual assertion	PMID:10595930
DOID:9256	colorectal cancer	HGNC:7127	Homo sapiens (human)	4292	MLH1	inference by association of genotype from phenotype used in manual assertion	PMID:10598809
DOID:9074	systemic lupus erythematosus	HGNC:2595	Homo sapiens (human)	1543	CYP1A1	inference by association of genotype from phenotype used in manual assertion	PMID:10599336 PMID:14611903 PMID:19561157
DOID:418	systemic scleroderma	HGNC:7646	Homo sapiens (human)	10	NAT2	inference by association of genotype from phenotype used in manual assertion	PMID:10599336
DOID:9074	systemic lupus erythematosus	HGNC:7646	Homo sapiens (human)	10	NAT2	inference by association of genotype from phenotype used in manual assertion	PMID:10599336
DOID:418	systemic scleroderma	HGNC:6709	Homo sapiens (human)	4049	LTA	inference by association of genotype from phenotype used in manual assertion	PMID:10600011
DOID:8466	retinal degeneration	HGNC:8824	Homo sapiens (human)	5176	SERPINF1	direct assay evidence used in manual assertion	PMID:10600408
DOID:12930	dilated cardiomyopathy	HGNC:5724	Homo sapiens (human)	3516	RBPJ	inference by association of genotype from phenotype used in manual assertion	PMID:10600520
DOID:2236	congenital afibrinogenemia	HGNC:3661	Homo sapiens (human)	2243	FGA	inference by association of genotype from phenotype used in manual assertion	PMID:10602365 PMID:15795544 RGD:7240710
DOID:11054	urinary bladder cancer	HGNC:3689	Homo sapiens (human)	2263	FGFR2	inference by association of genotype from phenotype used in manual assertion	PMID:10602477 PMID:16969861
DOID:1556	arthus reaction	RGD:2498	Rattus norvegicus (Norway rat)	54249	Cfd	direct assay evidence used in manual assertion	PMID:10605043
DOID:437	myasthenia gravis	HGNC:286	Homo sapiens (human)	154	ADRB2	inference by association of genotype from phenotype used in manual assertion	PMID:10606977
DOID:0110381	retinitis pigmentosa 14	MGI:109571	Mus musculus (house mouse)	22157	Tulp1	author statement supported by traceable reference	PMID:10607826
DOID:1024	leprosy	HGNC:10907	Homo sapiens (human)	6556	SLC11A1	inference by association of genotype from phenotype used in manual assertion	PMID:10608779 PMID:15755200
DOID:0110341	osteogenesis imperfecta type 2	MGI:88467	Mus musculus (house mouse)	12842	Col1a1	author statement supported by traceable reference	PMID:10608859 PMID:18248096
DOID:0110340	osteogenesis imperfecta type 4	MGI:88467	Mus musculus (house mouse)	12842	Col1a1	author statement supported by traceable reference	PMID:10608859 PMID:24443344 PMID:26277094
DOID:5844	myocardial infarction	HGNC:9204	Homo sapiens (human)	5444	PON1	inference by association of genotype from phenotype used in manual assertion	PMID:10610741 PMID:10978258
DOID:0090118	congenital amegakaryocytic thrombocytopenia	MGI:97076	Mus musculus (house mouse)	17480	Mpl	author statement supported by traceable reference	PMID:10611229
DOID:12134	factor VIII deficiency	HGNC:3546	Homo sapiens (human)	2157	F8	inference by association of genotype from phenotype used in manual assertion	PMID:10612839 PMID:16786531 RGD:7240710
DOID:0080006	bone development disease	HGNC:11908	Homo sapiens (human)	8792	TNFRSF11A	inference by association of genotype from phenotype used in manual assertion	PMID:10615125
DOID:5408	Paget's disease of bone	HGNC:11908	Homo sapiens (human)	8792	TNFRSF11A	inference by association of genotype from phenotype used in manual assertion	PMID:10615125
DOID:2256	osteochondrodysplasia	HGNC:12340	Homo sapiens (human)	7227	TRPS1	inference by association of genotype from phenotype used in manual assertion	PMID:10615131
DOID:0110859	polycystic kidney disease 2	MGI:1099818	Mus musculus (house mouse)	18764	Pkd2	author statement supported by traceable reference	PMID:10615132 PMID:12062060 PMID:28205547 PMID:9568711
DOID:8929	atrophic gastritis	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:10616761 PMID:20082482

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