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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 **10076 - 10100** 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:10652	Alzheimer's disease	HGNC:1318	Homo sapiens (human)	718	C3	inference by association of genotype from phenotype used in manual assertion	PMID:22300950
DOID:1441	autosomal dominant cerebellar ataxia	HGNC:1349	Homo sapiens (human)	219285	SAMD9L	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:2986	IgA glomerulonephritis	HGNC:8784	Homo sapiens (human)	8654	PDE5A	inference by association of genotype from phenotype used in manual assertion	PMID:20563733
DOID:3393	coronary artery disease	HGNC:3662	Homo sapiens (human)	2244	FGB	inference by association of genotype from phenotype used in manual assertion	PMID:8565160
DOID:0080208	metabolic dysfunction-associated steatotic liver disease	HGNC:9237	Homo sapiens (human)	10891	PPARGC1A	inference by association of genotype from phenotype used in manual assertion	PMID:23269818
DOID:11716	prediabetes syndrome	HGNC:1603	Homo sapiens (human)	729230	CCR2	inference by association of genotype from phenotype used in manual assertion	PMID:18096169
DOID:10629	microphthalmia	HGNC:6697	Homo sapiens (human)	4041	LRP5	inference by association of genotype from phenotype used in manual assertion	PMID:28111184
DOID:3393	coronary artery disease	HGNC:10718	Homo sapiens (human)	6401	SELE	inference by association of genotype from phenotype used in manual assertion	PMID:17578587
DOID:5082	liver cirrhosis	HGNC:2707	Homo sapiens (human)	1636	ACE	inference by association of genotype from phenotype used in manual assertion	PMID:19456900
DOID:0112313	brain small vessel disease	HGNC:3661	Homo sapiens (human)	2243	FGA	inference by association of genotype from phenotype used in manual assertion	PMID:17951283
DOID:8619	recurrent hypersomnia	HGNC:1938	Homo sapiens (human)	1120	CHKB	inference by association of genotype from phenotype used in manual assertion	PMID:19404393
DOID:5844	myocardial infarction	HGNC:543	Homo sapiens (human)	308	ANXA5	inference by association of genotype from phenotype used in manual assertion	PMID:12200370
DOID:9849	Meniere's disease	HGNC:5232	Homo sapiens (human)	3303	HSPA1A	inference by association of genotype from phenotype used in manual assertion	PMID:19241595
DOID:0111473	combined oxidative phosphorylation deficiency 5	HGNC:14508	Homo sapiens (human)	56945	MRPS22	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0070070	autosomal dominant intellectual developmental disorder 40	HGNC:20311	Homo sapiens (human)	283489	CHAMP1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:1307	dementia	HGNC:6700	Homo sapiens (human)	7804	LRP8	inference by association of genotype from phenotype used in manual assertion	PMID:17614163
DOID:0081453	Dent disease 1	HGNC:2023	Homo sapiens (human)	1184	CLCN5	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080652	calcium oxalate nephrolithiasis	HGNC:10993	Homo sapiens (human)	10861	SLC26A1	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0110820	hereditary spastic paraplegia 75	HGNC:6783	Homo sapiens (human)	4099	MAG	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050861	colorectal adenocarcinoma	HGNC:12828	Homo sapiens (human)	7515	XRCC1	inference by association of genotype from phenotype used in manual assertion	PMID:19908066
DOID:0080561	congenital disorder of glycosylation Ii	HGNC:23159	Homo sapiens (human)	85365	ALG2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:7575	pancreatic intraductal papillary-mucinous neoplasm	HGNC:11998	Homo sapiens (human)	7157	TP53	inference by association of genotype from phenotype used in manual assertion	PMID:28930868
DOID:0111918	spermatogenic failure 40	HGNC:25325	Homo sapiens (human)	255101	CFAP65	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080807	autosomal dominant craniodiaphyseal dysplasia	HGNC:13771	Homo sapiens (human)	50964	SOST	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050571	congenital disorder of glycosylation type II	HGNC:18619	Homo sapiens (human)	83548	COG3	inference by association of genotype from phenotype used in manual assertion	RGD:7240710

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