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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:0110960	Gaucher's disease perinatal lethal	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0112250	Gaucher's disease type IIIC	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0110957	Gaucher's disease type I	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0050474	Netherton syndrome	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:1926	Gaucher's disease	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0080855	Parkinsonism	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0110958	Gaucher's disease type II	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:8893	psoriasis	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:14330	Parkinson's disease	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0110959	Gaucher's disease type III	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0060892	late onset Parkinson's disease	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:12217	Lewy body dementia	WB:WBGene00021160	Caenorhabditis elegans	177314	gba-4	evidence used in automatic assertion	MGI:6194238
DOID:0110284	autosomal recessive limb-girdle muscular dystrophy type 2L	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0112379	muscular dystrophy-dystroglycanopathy type B4	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:9884	muscular dystrophy	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0110444	dilated cardiomyopathy 1X	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0050560	Walker-Warburg syndrome	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0050559	Fukuyama congenital muscular dystrophy	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0110296	autosomal recessive limb-girdle muscular dystrophy type 2M	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0110443	dilated cardiomyopathy 1B	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1	WB:WBGene00020924	Caenorhabditis elegans	189104	W02B3.4	evidence used in automatic assertion	MGI:6194238
DOID:0080563	congenital disorder of glycosylation Ik	WB:WBGene00020820	Caenorhabditis elegans	175920	algn-1	evidence used in automatic assertion	MGI:6194238
DOID:5212	congenital disorder of glycosylation	WB:WBGene00020820	Caenorhabditis elegans	175920	algn-1	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	WB:WBGene00020820	Caenorhabditis elegans	175920	algn-1	evidence used in automatic assertion	MGI:6194238
DOID:0081326	oxoglutarate dehydrogenase deficiency	WB:WBGene00020679	Caenorhabditis elegans	177235	ogdh-1	evidence used in automatic assertion	MGI:6194238

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