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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

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Disease ID	Disease Name	Alliance of Genome Resources ID ▼	Species	Gene ID	Gene Symbol	Evidence Code Names	References
DOID:0060227	Adams-Oliver syndrome	WB:WBGene00010386	Caenorhabditis elegans	179990	H12D21.10	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:0070254	congenital disorder of glycosylation type IIb	WB:WBGene00008775	Caenorhabditis elegans	177998	mogs-1	evidence used in automatic assertion	MGI:6194238
DOID:0060892	late onset Parkinson's disease	WB:WBGene00008706	Caenorhabditis elegans	178535	gba-3	evidence used in automatic assertion	MGI:6194238
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:0060284	paroxysmal nocturnal hemoglobinuria	WB:WBGene00008431	Caenorhabditis elegans	174386	piga-1	evidence used in automatic assertion	MGI:6194238
DOID:0060713	autosomal recessive congenital ichthyosis 4B	WB:WBGene00008431	Caenorhabditis elegans	174386	piga-1	evidence used in automatic assertion	MGI:6194238
DOID:0080139	multiple congenital anomalies-hypotonia-seizures syndrome 2	WB:WBGene00008431	Caenorhabditis elegans	174386	piga-1	evidence used in automatic assertion	MGI:6194238
DOID:0112315	brain small vessel disease 3	WB:WBGene00008426	Caenorhabditis elegans	3565069	D2045.9	evidence used in automatic assertion	MGI:6194238
DOID:0014667	disease of metabolism	WB:WBGene00008230	Caenorhabditis elegans	179335	pfk-1.2	evidence used in automatic assertion	MGI:6194238
DOID:2747	glycogen storage disease	WB:WBGene00008230	Caenorhabditis elegans	179335	pfk-1.2	evidence used in automatic assertion	MGI:6194238
DOID:11721	glycogen storage disease VII	WB:WBGene00008230	Caenorhabditis elegans	179335	pfk-1.2	evidence used in automatic assertion	MGI:6194238
DOID:0111458	galactose epimerase deficiency	WB:WBGene00008132	Caenorhabditis elegans	173171	gale-1	evidence used in automatic assertion	MGI:6194238

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