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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	nac	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	Gfr	CG9620	combinatorial experimental and author inference evidence used in manual assertion	PMID:16344471
DOID:0060041	autism spectrum disorder	HGNC:896	Homo sapiens (human)	553	AVPR1B		inference by association of genotype from phenotype used in manual assertion	PMID:27920663
DOID:0060639	permanent neonatal diabetes mellitus	HGNC:4195	Homo sapiens (human)	2645	GCK		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0090050	dystonia 27	HGNC:2213	Homo sapiens (human)	1293	COL6A3		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060239	Van der Woude syndrome	MGI:2655333	Mus musculus (house mouse)	230824	Grhl3		author statement supported by traceable reference	PMID:24360809
DOID:206	hereditary multiple exostoses	WB:WBGene00004360	Caenorhabditis elegans	178080	rib-1		mutant phenotype evidence used in manual assertion	PMID:17237233
DOID:2394	ovarian cancer	HGNC:12530	Homo sapiens (human)	54658	UGT1A1		inference by association of genotype from phenotype used in manual assertion	PMID:15254716 PMID:19299905
DOID:1612	breast cancer	HGNC:2596	Homo sapiens (human)	1544	CYP1A2		inference by association of genotype from phenotype used in manual assertion	PMID:18497059
DOID:12930	dilated cardiomyopathy	HGNC:3522	Homo sapiens (human)	2070	EYA4		inference by association of genotype from phenotype used in manual assertion	PMID:15735644
DOID:0050466	Loeys-Dietz syndrome	MGI:98729	Mus musculus (house mouse)	21813	Tgfbr2		author statement supported by traceable reference	PMID:24355923
DOID:0111787	frontometaphyseal dysplasia 2	HGNC:6859	Homo sapiens (human)	6885	MAP3K7		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0060581	Noonan syndrome 3	MGI:96680	Mus musculus (house mouse)	16653	Kras		author statement supported by traceable reference	PMID:25359213
DOID:543	dystonia	FB:FBgn0025615	Drosophila melanogaster (fruit fly)	31399	Torsin		combinatorial experimental and author inference evidence used in manual assertion	PMID:23583177 PMID:25887123
DOID:0050561	Lennox-Gastaut syndrome	MGI:2138334	Mus musculus (house mouse)	227333	Dgkd		author statement supported by traceable reference	PMID:17357084
DOID:0050908	myelodysplastic syndrome	HGNC:4886	Homo sapiens (human)	3077	HFE		inference by association of genotype from phenotype used in manual assertion	PMID:12624489
DOID:1596	depressive disorder	RGD:3057	Rattus norvegicus (Norway rat)	25635	Mc4r		mutant phenotype evidence used in manual assertion	PMID:18499089
DOID:0111028	hemochromatosis type 4	MGI:1315204	Mus musculus (house mouse)	53945	Slc40a1		author statement supported by traceable reference	PMID:17289807 PMID:25100063
DOID:0050791	persistent Mullerian duct syndrome	HGNC:464	Homo sapiens (human)	268	AMH		inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:7693	abdominal aortic aneurysm	HGNC:9204	Homo sapiens (human)	5444	PON1		inference by association of genotype from phenotype used in manual assertion	PMID:18635682
DOID:14040	autoimmune polyendocrine syndrome	HGNC:4942	Homo sapiens (human)	3117	HLA-DQA1		inference by association of genotype from phenotype used in manual assertion	PMID:12734793 PMID:16254435
DOID:0060746	basal laminar drusen	HGNC:4883	Homo sapiens (human)	3075	CFH		inference by association of genotype from phenotype used in manual assertion	RGD:7240710

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