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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 **451 - 475** 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:0110658	congenital myasthenic syndrome 15	SGD:S000000274	Saccharomyces cerevisiae S288C	852362	ALG14	evidence used in automatic assertion	MGI:6194238
DOID:0110658	congenital myasthenic syndrome 15	HGNC:28287	Homo sapiens (human)	199857	ALG14	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0080563	congenital disorder of glycosylation Ik	HGNC:37258	Homo sapiens (human)	644974	ALG1L2	evidence used in automatic assertion	MGI:6194238
DOID:5212	congenital disorder of glycosylation	HGNC:37258	Homo sapiens (human)	644974	ALG1L2	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	HGNC:37258	Homo sapiens (human)	644974	ALG1L2	evidence used in automatic assertion	MGI:6194238
DOID:0080561	congenital disorder of glycosylation Ii	SGD:S000003033	Saccharomyces cerevisiae S288C	852815	ALG2	evidence used in automatic assertion	MGI:6194238
DOID:0110669	congenital myasthenic syndrome 14	SGD:S000003033	Saccharomyces cerevisiae S288C	852815	ALG2	evidence used in automatic assertion	MGI:6194238
DOID:0080561	congenital disorder of glycosylation Ii	HGNC:23159	Homo sapiens (human)	85365	ALG2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0110669	congenital myasthenic syndrome 14	HGNC:23159	Homo sapiens (human)	85365	ALG2	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
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	HGNC:23056	Homo sapiens (human)	10195	ALG3	evidence used in automatic assertion	MGI:6194238
DOID:0080556	congenital disorder of glycosylation Id	HGNC:23056	Homo sapiens (human)	10195	ALG3	evidence used in automatic assertion inference by association of genotype from phenotype used in manual assertion	MGI:6194238 RGD:7240710
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:0050570	congenital disorder of glycosylation type I	HGNC:20266	Homo sapiens (human)	29880	ALG5	evidence used in automatic assertion	MGI:6194238
DOID:0080322	polycystic kidney disease	SGD:S000006148	Saccharomyces cerevisiae S288C	855874	ALG5	evidence used in automatic assertion	MGI:6194238
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000006148	Saccharomyces cerevisiae S288C	855874	ALG5	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:10359825
DOID:0080322	polycystic kidney disease	HGNC:20266	Homo sapiens (human)	29880	ALG5	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050570	congenital disorder of glycosylation type I	SGD:S000005528	Saccharomyces cerevisiae S288C	854163	ALG6	genetic interaction evidence used in manual assertion sequence similarity evidence used in manual assertion	PMID:10359825 PMID:10914684 PMID:10924277
DOID:0080555	congenital disorder of glycosylation Ic	HGNC:23157	Homo sapiens (human)	29929	ALG6	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050570	congenital disorder of glycosylation type I	HGNC:23157	Homo sapiens (human)	29929	ALG6	evidence used in automatic assertion	MGI:6194238
DOID:0080555	congenital disorder of glycosylation Ic	SGD:S000005528	Saccharomyces cerevisiae S288C	854163	ALG6	evidence used in automatic assertion	MGI:6194238
DOID:0110676	congenital myasthenic syndrome 13	SGD:S000000447	Saccharomyces cerevisiae S288C	852545	ALG7	evidence used in automatic assertion	MGI:6194238
DOID:0080562	congenital disorder of glycosylation Ij	SGD:S000000447	Saccharomyces cerevisiae S288C	852545	ALG7	evidence used in automatic assertion	MGI:6194238
DOID:0080560	congenital disorder of glycosylation Ih	HGNC:23161	Homo sapiens (human)	79053	ALG8	inference by association of genotype from phenotype used in manual assertion	RGD:7240710
DOID:0050770	polycystic liver disease	SGD:S000005593	Saccharomyces cerevisiae S288C	854233	ALG8	evidence used in automatic assertion	MGI:6194238

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