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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	January 28, 2025

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence ▲	References
DOID:1909	melanoma	SGD:S000000671	Saccharomyces cerevisiae S288C	850438	ERS1	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	sequence similarity evidence used in manual assertion	PMID:28357347 PMID:37060997
DOID:13317	hyperinsulinemic hypoglycemia	SGD:S000000545	Saccharomyces cerevisiae S288C	850317	GLK1	sequence similarity evidence used in manual assertion	PMID:37101203 PMID:38627865
DOID:162	cancer	SGD:S000000784	Saccharomyces cerevisiae S288C	856652	PCM1	sequence similarity evidence used in manual assertion	PMID:26354769
DOID:0070214	familial hyperinsulinemic hypoglycemia 7	SGD:S000000671	Saccharomyces cerevisiae S288C	850438	ERS1	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:9169	Wiskott-Aldrich syndrome	SGD:S000005707	Saccharomyces cerevisiae S288C	854353	LAS17	sequence similarity evidence used in manual assertion	PMID:16488394 PMID:19817875 PMID:35768435
DOID:0060041	autism spectrum disorder	SGD:S000005309	Saccharomyces cerevisiae S288C	855760	SEC12	sequence similarity evidence used in manual assertion	PMID:28542158
DOID:0050477	Liddle syndrome	SGD:S000000927	Saccharomyces cerevisiae S288C	856862	RSP5	sequence similarity evidence used in manual assertion	PMID:12684839
DOID:162	cancer	SGD:S000000233	Saccharomyces cerevisiae S288C	852317	CDS1	sequence similarity evidence used in manual assertion	PMID:26354769
DOID:1485	cystic fibrosis	SGD:S000001692	Saccharomyces cerevisiae S288C	853671	STE6	sequence similarity evidence used in manual assertion	PMID:7517933
DOID:1485	cystic fibrosis	SGD:S000001247	Saccharomyces cerevisiae S288C	856611	MNL1	sequence similarity evidence used in manual assertion	PMID:15215312
DOID:5212	congenital disorder of glycosylation	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	sequence similarity evidence used in manual assertion	PMID:10581255
DOID:9455	lipid storage disease	SGD:S000004232	Saccharomyces cerevisiae S288C	850943	ARV1	sequence similarity evidence used in manual assertion	PMID:24273168
DOID:3304	germinoma	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:0050427	xeroderma pigmentosum	SGD:S000002827	Saccharomyces cerevisiae S288C	852028	RAD30	sequence similarity evidence used in manual assertion	PMID:11743006
DOID:1324	lung cancer	SGD:S000001411	Saccharomyces cerevisiae S288C	854657	MLP2	sequence similarity evidence used in manual assertion	PMID:34793452
DOID:14213	hypophosphatasia	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:9256	colorectal cancer	SGD:S000000671	Saccharomyces cerevisiae S288C	850438	ERS1	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:162	cancer	SGD:S000006125	Saccharomyces cerevisiae S288C	855897	HRR25	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:0080552	congenital disorder of glycosylation Ia	SGD:S000001849	Saccharomyces cerevisiae S288C	850499	SEC53	sequence similarity evidence used in manual assertion	PMID:30530630 PMID:36214454
DOID:9870	galactosemia	SGD:S000000223	Saccharomyces cerevisiae S288C	852307	GAL10	sequence similarity evidence used in manual assertion	PMID:18188677 PMID:22613355
DOID:14791	Leber congenital amaurosis	SGD:S000005772	Saccharomyces cerevisiae S288C	854420	ENV9	sequence similarity evidence used in manual assertion	PMID:28540421
DOID:13994	cleidocranial dysplasia	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:0080556	congenital disorder of glycosylation Id	SGD:S000000178	Saccharomyces cerevisiae S288C	852196	ALG3	sequence similarity evidence used in manual assertion	PMID:23038983
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000000314	Saccharomyces cerevisiae S288C	852407	ALG1	sequence similarity evidence used in manual assertion	PMID:14709599 PMID:14973778 PMID:22966035

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