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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

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Disease ID	Disease Name	Alliance of Genome Resources ID	Species	Gene ID ▲	Gene Symbol	Evidence Code Names	References
DOID:1289	neurodegenerative disease	SGD:S000001554	Saccharomyces cerevisiae S288C	853792	OSI1	evidence used in automatic assertion	MGI:6194238
DOID:162	cancer	SGD:S000001542	Saccharomyces cerevisiae S288C	853806	MPE1	mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:30700905
DOID:162	cancer	SGD:S000001518	Saccharomyces cerevisiae S288C	853830	UGP1	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:26354769
DOID:0112218	developmental and epileptic encephalopathy 83	SGD:S000001518	Saccharomyces cerevisiae S288C	853830	UGP1	evidence used in automatic assertion	MGI:6194238
DOID:9256	colorectal cancer	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:0050861	colorectal adenocarcinoma	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:10591	pre-eclampsia	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:219	colon cancer	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:1184	nephrotic syndrome	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:3717	gastric adenocarcinoma	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:3021	acute kidney failure	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:0112298	spondylometaphyseal dysplasia Sedaghatian type	SGD:S000001509	Saccharomyces cerevisiae S288C	853842	GPX1	evidence used in automatic assertion	MGI:6194238
DOID:11446	sciatic neuropathy	SGD:S000001491	Saccharomyces cerevisiae S288C	853861	LAC1	evidence used in automatic assertion	MGI:6194238
DOID:0060718	autosomal recessive congenital ichthyosis 9	SGD:S000001491	Saccharomyces cerevisiae S288C	853861	LAC1	evidence used in automatic assertion	MGI:6194238
DOID:0111451	progressive myoclonus epilepsy 8	SGD:S000001491	Saccharomyces cerevisiae S288C	853861	LAC1	evidence used in automatic assertion	MGI:6194238
DOID:10652	Alzheimer's disease	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion	MGI:6194238
DOID:11252	microcytic anemia	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:37060997
DOID:1827	idiopathic generalized epilepsy	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion	MGI:6194238
DOID:0111223	centronuclear myopathy 1	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:37060997
DOID:854	collagen disease	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion	MGI:6194238
DOID:0112202	developmental and epileptic encephalopathy	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:37060997
DOID:409	liver disease	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion	MGI:6194238
DOID:986	alopecia areata	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion	MGI:6194238
DOID:0110197	Charcot-Marie-Tooth disease dominant intermediate B	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion mutant phenotype evidence used in manual assertion sequence similarity evidence used in manual assertion	MGI:6194238 PMID:37060997
DOID:0080437	developmental and epileptic encephalopathy 31A	SGD:S000001709	Saccharomyces cerevisiae S288C	853870	VPS1	evidence used in automatic assertion	MGI:6194238

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