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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 **901 - 925** 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:10579	leukodystrophy	SGD:S000000387	Saccharomyces cerevisiae S288C	852481	YPC1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:26792856
DOID:0080547	metabolic dysfunction-associated steatohepatitis	SGD:S000000387	Saccharomyces cerevisiae S288C	852481	YPC1	evidence used in automatic assertion	MGI:6194238
DOID:684	hepatocellular carcinoma	SGD:S000000387	Saccharomyces cerevisiae S288C	852481	YPC1	evidence used in automatic assertion	MGI:6194238
DOID:5212	congenital disorder of glycosylation	SGD:S000000314	Saccharomyces cerevisiae S288C	852407	ALG1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:24157261
DOID:0080563	congenital disorder of glycosylation Ik	SGD:S000000314	Saccharomyces cerevisiae S288C	852407	ALG1	evidence used in automatic assertion genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:26931382
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000000314	Saccharomyces cerevisiae S288C	852407	ALG1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:14709599 PMID:14973778 PMID:22966035
DOID:0110658	congenital myasthenic syndrome 15	SGD:S000000274	Saccharomyces cerevisiae S288C	852362	ALG14	evidence used in automatic assertion	MGI:6194238
DOID:1168	familial hyperlipidemia	SGD:S000000257	Saccharomyces cerevisiae S288C	852342	YBR053C	evidence used in automatic assertion	MGI:6194238
DOID:684	hepatocellular carcinoma	SGD:S000000257	Saccharomyces cerevisiae S288C	852342	YBR053C	evidence used in automatic assertion	MGI:6194238
DOID:10534	stomach cancer	SGD:S000000257	Saccharomyces cerevisiae S288C	852342	YBR053C	evidence used in automatic assertion	MGI:6194238
DOID:162	cancer	SGD:S000000233	Saccharomyces cerevisiae S288C	852317	CDS1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:26354769
DOID:0111458	galactose epimerase deficiency	SGD:S000000223	Saccharomyces cerevisiae S288C	852307	GAL10	evidence used in automatic assertion	MGI:6194238
DOID:9870	galactosemia	SGD:S000000223	Saccharomyces cerevisiae S288C	852307	GAL10	evidence used in automatic assertion genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:18188677 PMID:22613355
DOID:1588	thrombocytopenia	SGD:S000000223	Saccharomyces cerevisiae S288C	852307	GAL10	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:30247636
DOID:9870	galactosemia	SGD:S000000222	Saccharomyces cerevisiae S288C	852306	GAL7	evidence used in automatic assertion genetic interaction evidence used in manual assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:10799308 PMID:24077966 PMID:28213126 PMID:8794735
DOID:0111459	classic galactosemia	SGD:S000000222	Saccharomyces cerevisiae S288C	852306	GAL7	evidence used in automatic assertion	MGI:6194238
DOID:0070433	hyperphosphatasia with impaired intellectual development syndrome 1	SGD:S000000208	Saccharomyces cerevisiae S288C	852289	GPI18	evidence used in automatic assertion	MGI:6194238
DOID:0080566	congenital disorder of glycosylation In	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:18313027
DOID:162	cancer	SGD:S000000116	Saccharomyces cerevisiae S288C	852261	RFT1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:26354769
DOID:0080556	congenital disorder of glycosylation Id	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:23038983
DOID:5212	congenital disorder of glycosylation	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:10581255
DOID:9993	hypoglycemia	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:0070216	familial hyperinsulinemic hypoglycemia 3	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238
DOID:11714	gestational diabetes	SGD:S000002924	Saccharomyces cerevisiae S288C	852128	EMI2	evidence used in automatic assertion	MGI:6194238

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