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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	October 9, 2024

Displaying entries **69501 - 69525** of **71927** 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:0080072	intestinal pseudo-obstruction	SGD:S000004762	Saccharomyces cerevisiae S288C	855184	NUP53	evidence used in automatic assertion	MGI:6194238
DOID:11721	glycogen storage disease VII	SGD:S000004818	Saccharomyces cerevisiae S288C	855245	PFK2	evidence used in automatic assertion	MGI:6194238
DOID:0014667	disease of metabolism	SGD:S000004818	Saccharomyces cerevisiae S288C	855245	PFK2	evidence used in automatic assertion	MGI:6194238
DOID:2747	glycogen storage disease	SGD:S000004818	Saccharomyces cerevisiae S288C	855245	PFK2	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:7825568
DOID:0080000	muscular disease	SGD:S000004820	Saccharomyces cerevisiae S288C	855247	HFA1	evidence used in automatic assertion	MGI:6194238
DOID:0080547	metabolic dysfunction-associated steatohepatitis	SGD:S000004820	Saccharomyces cerevisiae S288C	855247	HFA1	evidence used in automatic assertion	MGI:6194238
DOID:0080208	metabolic dysfunction-associated steatotic liver disease	SGD:S000004820	Saccharomyces cerevisiae S288C	855247	HFA1	evidence used in automatic assertion	MGI:6194238
DOID:9970	obesity	SGD:S000004820	Saccharomyces cerevisiae S288C	855247	HFA1	evidence used in automatic assertion	MGI:6194238
DOID:9452	steatotic liver disease	SGD:S000004820	Saccharomyces cerevisiae S288C	855247	HFA1	evidence used in automatic assertion	MGI:6194238
DOID:0060404	chromosome 17q12 deletion syndrome	SGD:S000004820	Saccharomyces cerevisiae S288C	855247	HFA1	evidence used in automatic assertion	MGI:6194238
DOID:0050776	non-syndromic X-linked intellectual disability	SGD:S000004872	Saccharomyces cerevisiae S288C	855301	TRM732	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:25404562
DOID:9970	obesity	SGD:S000004872	Saccharomyces cerevisiae S288C	855301	TRM732	evidence used in automatic assertion	MGI:6194238
DOID:0080540	galactosialidosis	SGD:S000004912	Saccharomyces cerevisiae S288C	855343	PRC1	evidence used in automatic assertion	MGI:6194238
DOID:3211	lysosomal storage disease	SGD:S000004912	Saccharomyces cerevisiae S288C	855343	PRC1	evidence used in automatic assertion	MGI:6194238
DOID:684	hepatocellular carcinoma	SGD:S000004915	Saccharomyces cerevisiae S288C	855346	ADE4	evidence used in automatic assertion	MGI:6194238
DOID:4450	renal cell carcinoma	SGD:S000004915	Saccharomyces cerevisiae S288C	855346	ADE4	evidence used in automatic assertion	MGI:6194238
DOID:11832	visual epilepsy	SGD:S000004942	Saccharomyces cerevisiae S288C	855373	ERR3	evidence used in automatic assertion	MGI:6194238
DOID:10763	hypertension	SGD:S000004942	Saccharomyces cerevisiae S288C	855373	ERR3	evidence used in automatic assertion	MGI:6194238
DOID:14115	toxic shock syndrome	SGD:S000004942	Saccharomyces cerevisiae S288C	855373	ERR3	evidence used in automatic assertion	MGI:6194238
DOID:10652	Alzheimer's disease	SGD:S000004942	Saccharomyces cerevisiae S288C	855373	ERR3	evidence used in automatic assertion	MGI:6194238
DOID:0080855	Parkinsonism	SGD:S000004942	Saccharomyces cerevisiae S288C	855373	ERR3	evidence used in automatic assertion	MGI:6194238
DOID:1712	aortic valve stenosis	SGD:S000004942	Saccharomyces cerevisiae S288C	855373	ERR3	evidence used in automatic assertion	MGI:6194238
DOID:0110184	Charcot-Marie-Tooth disease type 4J	SGD:S000005269	Saccharomyces cerevisiae S288C	855392	FIG4	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:17572665
DOID:1289	neurodegenerative disease	SGD:S000005269	Saccharomyces cerevisiae S288C	855392	FIG4	evidence used in automatic assertion	MGI:6194238
DOID:0060589	Yunis-Varon syndrome	SGD:S000005269	Saccharomyces cerevisiae S288C	855392	FIG4	evidence used in automatic assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:37509182

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