GlyCosmos Portal

Table Filtering

Disease ID

Disease Name

Alliance of Genome Resources ID

Species

Gene ID

Gene Symbol

FlyGlycoDB

Evidence

References

Display
results per page.

Clear

Submissions

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 **9926 - 9950** of **14279** in total

« First

‹ Prev

…

394

395

396

397

398

399

400

401

402

…

Next ›

Last »
Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence	References
DOID:5419	schizophrenia	HGNC:4585	Homo sapiens (human)	2903	GRIN2A	direct assay evidence used in manual assertion	PMID:18534564
DOID:14330	Parkinson's disease	WB:WBGene00018878	Caenorhabditis elegans	180747	glit-1	combinatorial experimental and author inference evidence used in manual assertion	PMID:29346364
DOID:3393	coronary artery disease	HGNC:6700	Homo sapiens (human)	7804	LRP8	inference by association of genotype from phenotype used in manual assertion	PMID:17847002
DOID:0110026	age related macular degeneration 14	HGNC:1037	Homo sapiens (human)	629	CFB	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:13241	Behcet's disease	HGNC:7646	Homo sapiens (human)	10	NAT2	inference by association of genotype from phenotype used in manual assertion	PMID:15663505
DOID:13189	gout	HGNC:288	Homo sapiens (human)	155	ADRB3	inference by association of genotype from phenotype used in manual assertion	PMID:21285172
DOID:14784	olivopontocerebellar atrophy	HGNC:15984	Homo sapiens (human)	54840	APTX	inference by association of genotype from phenotype used in manual assertion	PMID:21465257
DOID:8929	atrophic gastritis	HGNC:820	Homo sapiens (human)	496	ATP4B	direct assay evidence used in manual assertion	PMID:30539573
DOID:1205	allergic disease	HGNC:3619	Homo sapiens (human)	2214	FCGR3A	mutant phenotype evidence used in manual assertion	PMID:22025730
DOID:0080159	Cryptococcal meningitis	HGNC:6922	Homo sapiens (human)	4153	MBL2	inference by association of genotype from phenotype used in manual assertion	PMID:21592999
DOID:12365	malaria	HGNC:613	Homo sapiens (human)	348	APOE	inference by association of genotype from phenotype used in manual assertion	PMID:24116184
DOID:12930	dilated cardiomyopathy	HGNC:15710	Homo sapiens (human)	11155	LDB3	inference by association of genotype from phenotype used in manual assertion	PMID:14660611 PMID:20852297
DOID:10763	hypertension	HGNC:285	Homo sapiens (human)	153	ADRB1	direct assay evidence used in manual assertion	PMID:20398560
DOID:5082	liver cirrhosis	HGNC:9605	Homo sapiens (human)	5743	PTGS2	mutant phenotype evidence used in manual assertion	PMID:29109031
DOID:10325	silicosis	RGD:621159	Rattus norvegicus (Norway rat)	60582	Il1rn	direct assay evidence used in manual assertion	PMID:23842733
DOID:2841	asthma	HGNC:11848	Homo sapiens (human)	7097	TLR2	inference by association of genotype from phenotype used in manual assertion	PMID:19096003 PMID:19148143 PMID:20685742 PMID:20815312 PMID:22402138
DOID:0070529	Sifrim-Hitz-Weiss syndrome	HGNC:1919	Homo sapiens (human)	1108	CHD4	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0111647	Schopf-Schulz-Passarge syndrome	HGNC:13829	Homo sapiens (human)	80326	WNT10A	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:1936	atherosclerosis	HGNC:7876	Homo sapiens (human)	4846	NOS3	inference by association of genotype from phenotype used in manual assertion	PMID:21114134
DOID:8947	diabetic retinopathy	HGNC:11181	Homo sapiens (human)	6649	SOD3	direct assay evidence used in manual assertion	PMID:12663605
DOID:0050908	myelodysplastic syndrome	MGI:2684063	Mus musculus (house mouse)	228790	Asxl1	author statement supported by traceable reference	PMID:24218140 PMID:24255920 PMID:29113963
DOID:11832	visual epilepsy	RGD:621237	Rattus norvegicus (Norway rat)	25625	Tnfrsf1a	direct assay evidence used in manual assertion	PMID:23333565
DOID:3328	temporal lobe epilepsy	MGI:96654	Mus musculus (house mouse)	16485	Kcna1	author statement supported by traceable reference	PMID:24270080
DOID:0080785	Brown-Vialetto-Van Laere syndrome 1	HGNC:16187	Homo sapiens (human)	113278	SLC52A3	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080960	amelogenesis imperfecta type 2A6	HGNC:4519	Homo sapiens (human)	8111	GPR68	inference by association of genotype from phenotype used in manual assertion	RGD:7240710

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

International Collaboration

Acknowledgements