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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 **26 - 50** of **14279** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	FlyGlycoDB ▲	Evidence	References
DOID:14227	azoospermia	FB:FBgn0020251	Drosophila melanogaster (fruit fly)	38736	sfl	CG8339	combinatorial experimental and author inference evidence used in manual assertion	PMID:25361961
DOID:0050161	lower respiratory tract disease	FB:FBgn0030695	Drosophila melanogaster (fruit fly)	32534	PGRP-LE	CG8995	combinatorial experimental and author inference evidence used in manual assertion	PMID:33826881
DOID:0060050	autoimmune disease of blood	FB:FBgn0032078	Drosophila melanogaster (fruit fly)	34215	C1GalTA	CG9520	combinatorial experimental and author inference evidence used in manual assertion	PMID:25779703
DOID:0050571	congenital disorder of glycosylation type II	FB:FBgn0265351	Drosophila melanogaster (fruit fly)	40981	Gfr	CG9620	combinatorial experimental and author inference evidence used in manual assertion	PMID:16344471
DOID:0050571	congenital disorder of glycosylation type II	FB:FBgn0265351	Drosophila melanogaster (fruit fly)	40981	nac	CG9620	combinatorial experimental and author inference evidence used in manual assertion	PMID:16344471
DOID:3393	coronary artery disease	HGNC:18590	Homo sapiens (human)	80339	PNPLA3		inference by association of genotype from phenotype used in manual assertion	PMID:31377187
DOID:0070119	Meckel syndrome 5	HGNC:29168	Homo sapiens (human)	23322	RPGRIP1L		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:3910	lung adenocarcinoma	HGNC:9646	Homo sapiens (human)	5783	PTPN13		inference by association of genotype from phenotype used in manual assertion	PMID:19672627
DOID:0080074	neural tube defect	HGNC:1550	Homo sapiens (human)	875	CBS		inference by association of genotype from phenotype used in manual assertion	PMID:12649066
DOID:12206	dengue hemorrhagic fever	HGNC:11050	Homo sapiens (human)	6532	SLC6A4		inference by association of genotype from phenotype used in manual assertion	PMID:30452889
DOID:0090003	agenesis of the corpus callosum with peripheral neuropathy	MGI:2135960	Mus musculus (house mouse)	107723	Slc12a6		author statement supported by traceable reference	PMID:12368912 PMID:14532115 PMID:22423107
DOID:2349	arteriosclerosis	HGNC:11850	Homo sapiens (human)	7099	TLR4		inference by association of genotype from phenotype used in manual assertion	PMID:16890863
DOID:8923	skin melanoma	HGNC:1101	Homo sapiens (human)	675	BRCA2		inference by association of genotype from phenotype used in manual assertion	PMID:25243787
DOID:1289	neurodegenerative disease	FB:FBgn0001075	Drosophila melanogaster (fruit fly)	33627	ft		combinatorial experimental and author inference evidence used in manual assertion	PMID:21278706
DOID:0070238	primary coenzyme Q10 deficiency 1	HGNC:25223	Homo sapiens (human)	27235	COQ2		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:11555	Fuchs' endothelial dystrophy	HGNC:2216	Homo sapiens (human)	1296	COL8A2		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:9952	acute lymphoblastic leukemia	HGNC:9204	Homo sapiens (human)	5444	PON1		inference by association of genotype from phenotype used in manual assertion	PMID:22976839
DOID:576	proteinuria	RGD:2988	Rattus norvegicus (Norway rat)	25473	Lamb2		mutant phenotype evidence used in manual assertion	PMID:21511833
DOID:12554	hemolytic-uremic syndrome	MGI:88385	Mus musculus (house mouse)	12628	Cfh		author statement supported by traceable reference	PMID:17517971
DOID:850	lung disease	HGNC:7646	Homo sapiens (human)	10	NAT2		inference by association of genotype from phenotype used in manual assertion	PMID:8961976
DOID:2671	transitional cell carcinoma	HGNC:5472	Homo sapiens (human)	3486	IGFBP3		direct assay evidence used in manual assertion	PMID:17541304
DOID:11758	iron deficiency anemia	HGNC:11740	Homo sapiens (human)	7018	TF		inference by association of genotype from phenotype used in manual assertion	PMID:11703331
DOID:0080015	physical disorder	MGI:88180	Mus musculus (house mouse)	12159	Bmp4		author statement supported by traceable reference	PMID:23028455
DOID:0070552	epidermolytic palmoplantar keratoderma 1	HGNC:6447	Homo sapiens (human)	3857	KRT9		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:289	endometriosis	RGD:620349	Rattus norvegicus (Norway rat)	29527	Ptgs2		mutant phenotype evidence used in manual assertion	PMID:20056215

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