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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

Displaying entries **126 - 150** of **14279** in total

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID	Gene Symbol	Evidence ▼	References
DOID:0050524	maturity-onset diabetes of the young	SGD:S000000545	Saccharomyces cerevisiae S288C	850317	GLK1	sequence similarity evidence used in manual assertion	PMID:37101203 PMID:38627865
DOID:0080001	bone disease	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:162	cancer	SGD:S000002457	Saccharomyces cerevisiae S288C	851620	TPI1	sequence similarity evidence used in manual assertion	PMID:26354769
DOID:0080572	congenital disorder of glycosylation Iw	SGD:S000002990	Saccharomyces cerevisiae S288C	852862	STT3	sequence similarity evidence used in manual assertion	PMID:34653363
DOID:1612	breast cancer	SGD:S000006387	Saccharomyces cerevisiae S288C	856313	DPM1	sequence similarity evidence used in manual assertion	PMID:30637701
DOID:0110914	infantile hypophosphatasia	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:162	cancer	SGD:S000000935	Saccharomyces cerevisiae S288C	856870	GLC7	sequence similarity evidence used in manual assertion	PMID:26354769
DOID:0050776	non-syndromic X-linked intellectual disability	SGD:S000004872	Saccharomyces cerevisiae S288C	855301	TRM732	sequence similarity evidence used in manual assertion	PMID:25404562
DOID:2750	glycogen storage disease IV	SGD:S000000737	Saccharomyces cerevisiae S288C	856705	GLC3	sequence similarity evidence used in manual assertion	PMID:8463281
DOID:11724	limb-girdle muscular dystrophy	SGD:S000006012	Saccharomyces cerevisiae S288C	856014	GLR1	sequence similarity evidence used in manual assertion	PMID:30515627
DOID:4440	seminoma	SGD:S000002889	Saccharomyces cerevisiae S288C	852092	PHO8	sequence similarity evidence used in manual assertion	PMID:25860149
DOID:14330	Parkinson's disease	SGD:S000003394	Saccharomyces cerevisiae S288C	853071	TIF4631	sequence similarity evidence used in manual assertion	PMID:25533483
DOID:1289	neurodegenerative disease	WB:WBGene00004033	Caenorhabditis elegans	181166	pkc-2	sequence orthology evidence used in manual assertion	PMID:28716951
DOID:2978	carbohydrate metabolic disorder	WB:WBGene00001645	Caenorhabditis elegans	179562	gly-20	sequence orthology evidence used in manual assertion	PMID:35586945
DOID:1287	cardiovascular system disease	WB:WBGene00011480	Caenorhabditis elegans	178014	enpl-1	sequence orthology evidence used in manual assertion	PMID:38553458
DOID:0090117	thiamine-responsive megaloblastic anemia syndrome	WB:WBGene00018138	Caenorhabditis elegans	178745	folt-2	sequence orthology evidence used in manual assertion	PMID:17475669
DOID:12798	mucopolysaccharidosis	WB:WBGene00010722	Caenorhabditis elegans	175063	K09E4.4	sequence orthology evidence used in manual assertion	WB:WBPaper00035542
DOID:0060363	glycerol kinase deficiency	WB:WBGene00020007	Caenorhabditis elegans	173747	R11F4.1	sequence orthology evidence used in manual assertion	PMID:10767309
DOID:0050659	biotin-responsive basal ganglia disease	WB:WBGene00044738	Caenorhabditis elegans	4363081	folt-3	sequence alignment evidence used in manual assertion	PMID:17475669
DOID:576	proteinuria	RGD:2988	Rattus norvegicus (Norway rat)	25473	Lamb2	mutant phenotype evidence used in manual assertion	PMID:21511833
DOID:289	endometriosis	RGD:620349	Rattus norvegicus (Norway rat)	29527	Ptgs2	mutant phenotype evidence used in manual assertion	PMID:20056215
DOID:3525	middle cerebral artery infarction	RGD:3726	Rattus norvegicus (Norway rat)	25273	Smo	mutant phenotype evidence used in manual assertion	PMID:23499832 PMID:23696546
DOID:219	colon cancer	HGNC:28611	Homo sapiens (human)	253260	RICTOR	mutant phenotype evidence used in manual assertion	PMID:20226010
DOID:3070	high grade glioma	HGNC:8800	Homo sapiens (human)	5155	PDGFB	mutant phenotype evidence used in manual assertion	PMID:21677873 PMID:26945107
DOID:0060180	colitis	RGD:3812	Rattus norvegicus (Norway rat)	25007	Tacr2	mutant phenotype evidence used in manual assertion	PMID:12490601

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