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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:0050866	oral squamous cell carcinoma	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:0060108	brain glioma	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:3319	lymphangioleiomyomatosis	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:10652	Alzheimer's disease	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:8947	diabetic retinopathy	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:0050827	rheumatic heart disease	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:1826	epilepsy	SGD:S000003769	Saccharomyces cerevisiae S288C	853465	TDH2	evidence used in automatic assertion	MGI:6194238
DOID:0081097	Rafiq syndrome	SGD:S000003892	Saccharomyces cerevisiae S288C	853595	MNS1	evidence used in automatic assertion	MGI:6194238
DOID:0050588	muscular dystrophy-dystroglycanopathy type B1	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0110297	autosomal recessive limb-girdle muscular dystrophy type 2K	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0111237	congenital muscular dystrophy-dystroglycanopathy type A1	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0050560	Walker-Warburg syndrome	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:27358400
DOID:0112374	muscular dystrophy-dystroglycanopathy	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0050453	lissencephaly	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:0050700	cardiomyopathy	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:9884	muscular dystrophy	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:9296	cleft lip	SGD:S000003904	Saccharomyces cerevisiae S288C	853608	PMT4	evidence used in automatic assertion	MGI:6194238
DOID:83	cataract	SGD:S000003920	Saccharomyces cerevisiae S288C	853624	SOR1	evidence used in automatic assertion	MGI:6194238
DOID:9743	diabetic neuropathy	SGD:S000003920	Saccharomyces cerevisiae S288C	853624	SOR1	evidence used in automatic assertion	MGI:6194238
DOID:0081427	autosomal recessive distal hereditary motor neuronopathy 8	SGD:S000003920	Saccharomyces cerevisiae S288C	853624	SOR1	evidence used in automatic assertion	MGI:6194238
DOID:0081376	obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy	SGD:S000003920	Saccharomyces cerevisiae S288C	853624	SOR1	evidence used in automatic assertion	MGI:6194238
DOID:0081133	3-methylglutaconic aciduria type 7a	SGD:S000003949	Saccharomyces cerevisiae S288C	850633	HSP104	evidence used in automatic assertion	MGI:6194238
DOID:0081134	3-methylglutaconic aciduria type 7b	SGD:S000003949	Saccharomyces cerevisiae S288C	850633	HSP104	evidence used in automatic assertion	MGI:6194238
DOID:0050590	severe congenital neutropenia	SGD:S000003949	Saccharomyces cerevisiae S288C	850633	HSP104	evidence used in automatic assertion	MGI:6194238

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