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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 **13201 - 13225** 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:3454	brain infarction	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:11798899
DOID:10763	hypertension	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1	inference by association of genotype from phenotype used in manual assertion	PMID:11798899
DOID:5844	myocardial infarction	HGNC:8823	Homo sapiens (human)	5175	PECAM1	inference by association of genotype from phenotype used in manual assertion	PMID:11795274 PMID:15488875
DOID:3393	coronary artery disease	HGNC:8823	Homo sapiens (human)	5175	PECAM1	inference by association of genotype from phenotype used in manual assertion	PMID:11795274 PMID:12732396
DOID:9352	type 2 diabetes mellitus	HGNC:9291	Homo sapiens (human)	5506	PPP1R3A	mutant phenotype evidence used in manual assertion	PMID:11793847
DOID:9352	type 2 diabetes mellitus	HGNC:983	Homo sapiens (human)	590	BCHE	inference by association of genotype from phenotype used in manual assertion	PMID:11793025
DOID:0060162	dentatorubral-pallidoluysian atrophy	FB:FBgn0010825	Drosophila melanogaster (fruit fly)	46156	Gug	combinatorial experimental and author inference evidence used in manual assertion	PMID:11792320 PMID:20339376
DOID:0050144	Kartagener syndrome	HGNC:2950	Homo sapiens (human)	1767	DNAH5	inference by association of genotype from phenotype used in manual assertion	PMID:11788826
DOID:529	blepharospasm	HGNC:3026	Homo sapiens (human)	1816	DRD5	inference by association of genotype from phenotype used in manual assertion	PMID:11781417
DOID:9351	diabetes mellitus	MGI:104740	Mus musculus (house mouse)	19013	Ppara	author statement supported by traceable reference	PMID:11781357
DOID:12894	Sjogren's syndrome	MGI:1344376	Mus musculus (house mouse)	24099	Tnfsf13b	author statement supported by traceable reference	PMID:11781351
DOID:10325	silicosis	HGNC:4944	Homo sapiens (human)	3119	HLA-DQB1	inference by association of genotype from phenotype used in manual assertion	PMID:11776400
DOID:14115	toxic shock syndrome	HGNC:11760	Homo sapiens (human)	7035	TFPI	direct assay evidence used in manual assertion	PMID:11776329
DOID:2451	protein S deficiency	HGNC:9456	Homo sapiens (human)	5627	PROS1	inference by association of genotype from phenotype used in manual assertion	PMID:11776305 PMID:16885060 PMID:19466456 PMID:22261441 PMID:7579448 PMID:9657428
DOID:13809	familial combined hyperlipidemia	HGNC:243	Homo sapiens (human)	118	ADD1	inference by association of genotype from phenotype used in manual assertion	PMID:11775124
DOID:10487	Hirschsprung's disease	MGI:107430	Mus musculus (house mouse)	14573	Gdnf	author statement supported by traceable reference	PMID:11774071 PMID:12668632 PMID:8657307
DOID:0110953	Waardenburg syndrome type 4A	MGI:102720	Mus musculus (house mouse)	13618	Ednrb	author statement supported by traceable reference	PMID:11773966 PMID:15294878
DOID:0050127	sinusitis	HGNC:1884	Homo sapiens (human)	1080	CFTR	inference by association of genotype from phenotype used in manual assertion	PMID:11773581
DOID:10584	retinitis pigmentosa	HGNC:17348	Homo sapiens (human)	9129	PRPF3	inference by association of genotype from phenotype used in manual assertion	PMID:11773002
DOID:10584	retinitis pigmentosa	MGI:98488	Mus musculus (house mouse)	21366	Slc6a6	author statement supported by traceable reference	PMID:11772953
DOID:10952	nephritis	HGNC:11158	Homo sapiens (human)	6632	SNRPD1	direct assay evidence used in manual assertion	PMID:11771960
DOID:14789	spondyloepiphyseal dysplasia congenita	MGI:88452	Mus musculus (house mouse)	12824	Col2a1	author statement supported by traceable reference	PMID:11771668 PMID:12968670 PMID:22028304 PMID:25917818 PMID:7590256
DOID:10808	gastric ulcer	RGD:3239	Rattus norvegicus (Norway rat)	25342	Oxtr	mutant phenotype evidence used in manual assertion	PMID:11764003
DOID:9352	type 2 diabetes mellitus	HGNC:9642	Homo sapiens (human)	5770	PTPN1	inference by association of genotype from phenotype used in manual assertion	PMID:11756316 RGD:7240710
DOID:4450	renal cell carcinoma	HGNC:11796	Homo sapiens (human)	7067	THRA	inference by association of genotype from phenotype used in manual assertion	PMID:11756220

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