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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 **3201 - 3225** 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:3121	gallbladder cancer	HGNC:2593	Homo sapiens (human)	1586	CYP17A1	inference by association of genotype from phenotype used in manual assertion	PMID:16381022
DOID:10211	cholelithiasis	HGNC:2593	Homo sapiens (human)	1586	CYP17A1	inference by association of genotype from phenotype used in manual assertion	PMID:16381022
DOID:0080010	bone structure disease	MGI:2677633	Mus musculus (house mouse)	229214	Qrfpr	author statement supported by traceable reference	PMID:16382160
DOID:0090031	D-bifunctional protein deficiency	HGNC:5213	Homo sapiens (human)	3295	HSD17B4	inference by association of genotype from phenotype used in manual assertion	PMID:16385454 PMID:9345094 RGD:7240710
DOID:783	end stage renal disease	HGNC:2707	Homo sapiens (human)	1636	ACE	inference by association of genotype from phenotype used in manual assertion	PMID:16385653 PMID:20149750
DOID:2841	asthma	HGNC:5980	Homo sapiens (human)	3603	IL16	inference by association of genotype from phenotype used in manual assertion	PMID:16387589
DOID:1094	attention deficit hyperactivity disorder	HGNC:12008	Homo sapiens (human)	7166	TPH1	inference by association of genotype from phenotype used in manual assertion	PMID:16389593 PMID:20921119
DOID:0050742	nicotine dependence	HGNC:2228	Homo sapiens (human)	1312	COMT	inference by association of genotype from phenotype used in manual assertion	PMID:16395295 PMID:16499480 PMID:16876132 PMID:17206495 PMID:20188797 PMID:28472995
DOID:9352	type 2 diabetes mellitus	RGD:2644	Rattus norvegicus (Norway rat)	25634	G6pc1	direct assay evidence used in manual assertion	PMID:16396963
DOID:3312	bipolar disorder	HGNC:4617	Homo sapiens (human)	2932	GSK3B	inference by association of genotype from phenotype used in manual assertion	PMID:16397405 PMID:17357145
DOID:5419	schizophrenia	HGNC:4617	Homo sapiens (human)	2932	GSK3B	inference by association of genotype from phenotype used in manual assertion	PMID:16397405
DOID:3627	aortic aneurysm	RGD:62058	Rattus norvegicus (Norway rat)	29473	Aoc3	mutant phenotype evidence used in manual assertion	PMID:16397885
DOID:9351	diabetes mellitus	HGNC:7646	Homo sapiens (human)	10	NAT2	inference by association of genotype from phenotype used in manual assertion	PMID:16397907
DOID:3083	chronic obstructive pulmonary disease	HGNC:11181	Homo sapiens (human)	6649	SOD3	inference by association of genotype from phenotype used in manual assertion	PMID:16399992
DOID:1742	drug psychosis	HGNC:8156	Homo sapiens (human)	4988	OPRM1	inference by association of genotype from phenotype used in manual assertion	PMID:16402083
DOID:114	heart disease	MGI:95489	Mus musculus (house mouse)	14118	Fbn1	author statement supported by traceable reference	PMID:16407178
DOID:9255	frontotemporal dementia	HGNC:6893	Homo sapiens (human)	4137	MAPT	mutant phenotype evidence used in manual assertion	PMID:16407562
DOID:409	liver disease	HGNC:404	Homo sapiens (human)	217	ALDH2	inference by association of genotype from phenotype used in manual assertion	PMID:16408483
DOID:12306	vitiligo	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:16409268
DOID:0081267	graft-versus-host disease	HGNC:5438	Homo sapiens (human)	3458	IFNG	inference by association of genotype from phenotype used in manual assertion	PMID:16409297 PMID:19747638
DOID:0060574	von Willebrand's disease 2	HGNC:6137	Homo sapiens (human)	3673	ITGA2	inference by association of genotype from phenotype used in manual assertion	PMID:16409463
DOID:1067	open-angle glaucoma	HGNC:9204	Homo sapiens (human)	5444	PON1	inference by association of genotype from phenotype used in manual assertion	PMID:16411107
DOID:5844	myocardial infarction	HGNC:3530	Homo sapiens (human)	2161	F12	inference by association of genotype from phenotype used in manual assertion	PMID:16411408
DOID:12894	Sjogren's syndrome	MGI:96556	Mus musculus (house mouse)	16189	Il4	author statement supported by traceable reference	PMID:16413168
DOID:10763	hypertension	RGD:3876	Rattus norvegicus (Norway rat)	24835	Tnf	mutant phenotype evidence used in manual assertion	PMID:16415373

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