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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:13375	temporal arteritis	HGNC:6014	Homo sapiens (human)	3565	IL4	inference by association of genotype from phenotype used in manual assertion	PMID:15570643
DOID:3883	Lynch syndrome	HGNC:7329	Homo sapiens (human)	2956	MSH6	inference by association of genotype from phenotype used in manual assertion	PMID:15571801 PMID:28218421 PMID:7604266
DOID:13603	obstructive jaundice	RGD:3645	Rattus norvegicus (Norway rat)	24770	Ccl2	direct assay evidence used in manual assertion	PMID:15573249
DOID:3526	cerebral infarction	HGNC:11784	Homo sapiens (human)	7056	THBD	inference by association of genotype from phenotype used in manual assertion	PMID:15574195
DOID:0070355	overactive bladder syndrome	RGD:620401	Rattus norvegicus (Norway rat)	81509	Bdkrb1	mutant phenotype evidence used in manual assertion	PMID:15576455
DOID:10892	hypospadias	HGNC:2595	Homo sapiens (human)	1543	CYP1A1	inference by association of genotype from phenotype used in manual assertion	PMID:15579657
DOID:4483	rhinitis	HGNC:10623	Homo sapiens (human)	6369	CCL24	inference by association of genotype from phenotype used in manual assertion	PMID:15580493
DOID:9351	diabetes mellitus	HGNC:4271	Homo sapiens (human)	2696	GIPR	mutant phenotype evidence used in manual assertion	PMID:15582721
DOID:10652	Alzheimer's disease	HGNC:6547	Homo sapiens (human)	3949	LDLR	inference by association of genotype from phenotype used in manual assertion	PMID:15585340 PMID:15689450 PMID:17239995
DOID:0080855	Parkinsonism	HGNC:5232	Homo sapiens (human)	3303	HSPA1A	mutant phenotype evidence used in manual assertion	PMID:15585408
DOID:12971	hereditary spherocytosis	HGNC:3381	Homo sapiens (human)	2038	EPB42	inference by association of genotype from phenotype used in manual assertion	PMID:1558976
DOID:0050700	cardiomyopathy	HGNC:11180	Homo sapiens (human)	6648	SOD2	inference by association of genotype from phenotype used in manual assertion	PMID:15591282
DOID:0110826	Usher syndrome type 1	HGNC:7606	Homo sapiens (human)	4647	MYO7A	inference by association of genotype from phenotype used in manual assertion	PMID:15592175
DOID:8893	psoriasis	MGI:103038	Mus musculus (house mouse)	20848	Stat3	author statement supported by traceable reference	PMID:15592573
DOID:1591	renovascular hypertension	RGD:2059	Rattus norvegicus (Norway rat)	24925	Adrb1	direct assay evidence used in manual assertion	PMID:15592645
DOID:0090004	progressive pseudorheumatoid arthropathy of childhood	MGI:2685581	Mus musculus (house mouse)	327743	Ccn6	author statement supported by traceable reference	PMID:15601861 PMID:24040393
DOID:0050425	restless legs syndrome	MGI:94925	Mus musculus (house mouse)	13490	Drd3	author statement supported by traceable reference	PMID:15601940
DOID:10603	glucose intolerance	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:15602651
DOID:1612	breast cancer	HGNC:3467	Homo sapiens (human)	2099	ESR1	inference by association of genotype from phenotype used in manual assertion	PMID:15604249 PMID:17553133 PMID:19320640 PMID:19636371 RGD:7240710
DOID:3407	carotid artery disease	HGNC:12518	Homo sapiens (human)	7351	UCP2	inference by association of genotype from phenotype used in manual assertion	PMID:15604415
DOID:8483	retinal artery occlusion	HGNC:6018	Homo sapiens (human)	3569	IL6	inference by association of genotype from phenotype used in manual assertion	PMID:15604420
DOID:4535	hypotrichosis	RGD:735015	Rattus norvegicus (Norway rat)	291754	Dsg4	mutant phenotype evidence used in manual assertion	PMID:15606503
DOID:3012	Li-Fraumeni syndrome	MGI:98834	Mus musculus (house mouse)	22059	Trp53	author statement supported by traceable reference	PMID:15607980 PMID:15607981 PMID:7922305
DOID:384	Wolff-Parkinson-White syndrome	HGNC:9386	Homo sapiens (human)	51422	PRKAG2	mutant phenotype evidence used in manual assertion	PMID:15611370
DOID:2841	asthma	HGNC:4964	Homo sapiens (human)	3135	HLA-G	inference by association of genotype from phenotype used in manual assertion	PMID:15611928 RGD:7240710

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