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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	July 29, 2024

Displaying entries **10851 - 10875** of **12216** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID ▲	Species	Gene ID	Gene Symbol	Evidence Code Names	References
DOID:8893	psoriasis	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:1926	Gaucher's disease	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0080855	Parkinsonism	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0112250	Gaucher's disease type IIIC	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0110957	Gaucher's disease type I	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0050474	Netherton syndrome	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0110959	Gaucher's disease type III	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:14330	Parkinson's disease	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0110960	Gaucher's disease perinatal lethal	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0110958	Gaucher's disease type II	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:12217	Lewy body dementia	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
DOID:0070254	congenital disorder of glycosylation type IIb	WB:WBGene00008775	Caenorhabditis elegans	177998	mogs-1	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	WB:WBGene00009925	Caenorhabditis elegans	178364	F52B11.2	evidence used in automatic assertion	MGI:6194238
DOID:5212	congenital disorder of glycosylation	WB:WBGene00009925	Caenorhabditis elegans	178364	F52B11.2	evidence used in automatic assertion	MGI:6194238
DOID:0080552	congenital disorder of glycosylation Ia	WB:WBGene00009925	Caenorhabditis elegans	178364	F52B11.2	evidence used in automatic assertion	MGI:6194238
DOID:0060227	Adams-Oliver syndrome	WB:WBGene00010386	Caenorhabditis elegans	179990	H12D21.10	evidence used in automatic assertion	MGI:6194238
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1	WB:WBGene00010694	Caenorhabditis elegans	3565692	bgnt-1.5	evidence used in automatic assertion	MGI:6194238
DOID:0111238	congenital muscular dystrophy-dystroglycanopathy type A13	WB:WBGene00010694	Caenorhabditis elegans	3565692	bgnt-1.5	evidence used in automatic assertion	MGI:6194238
DOID:0111242	congenital muscular dystrophy-dystroglycanopathy type A6	WB:WBGene00010716	Caenorhabditis elegans	187206	lge-1	evidence used in automatic assertion	MGI:6194238
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1	WB:WBGene00010716	Caenorhabditis elegans	187206	lge-1	evidence used in automatic assertion	MGI:6194238
DOID:0110637	muscular dystrophy-dystroglycanopathy type B6	WB:WBGene00010716	Caenorhabditis elegans	187206	lge-1	evidence used in automatic assertion	MGI:6194238
DOID:11727	facioscapulohumeral muscular dystrophy	WB:WBGene00010716	Caenorhabditis elegans	187206	lge-1	evidence used in automatic assertion	MGI:6194238
DOID:5212	congenital disorder of glycosylation	WB:WBGene00010720	Caenorhabditis elegans	175065	algn-3	evidence used in automatic assertion	MGI:6194238
DOID:0080556	congenital disorder of glycosylation Id	WB:WBGene00010720	Caenorhabditis elegans	175065	algn-3	evidence used in automatic assertion	MGI:6194238
DOID:14250	Down syndrome	WB:WBGene00010757	Caenorhabditis elegans	259529	pad-2	combinatorial experimental and author inference evidence used in manual assertion mutant phenotype evidence used in manual assertion	PMID:15233996

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