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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 451 - 475 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0080832 mild cognitive impairment HGNC:320 Homo sapiens (human) 177 AGER direct assay evidence used in manual assertion
  • PMID:22415896
DOID:576 proteinuria HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:12606536
DOID:8893 psoriasis HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:12029499
DOID:784 chronic kidney disease HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:20185929
  • PMID:20353610
  • PMID:23593165
DOID:13564 aspergillosis HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:22114731
DOID:3393 coronary artery disease HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:20668462
DOID:784 chronic kidney disease HGNC:320 Homo sapiens (human) 177 AGER direct assay evidence used in manual assertion
  • PMID:21432860
DOID:3021 acute kidney failure HGNC:320 Homo sapiens (human) 177 AGER direct assay evidence used in manual assertion
  • PMID:21811803
DOID:0080162 lupus nephritis HGNC:320 Homo sapiens (human) 177 AGER inference by association of genotype from phenotype used in manual assertion
  • PMID:22513366
DOID:0080132 Sengers syndrome HGNC:21869 Homo sapiens (human) 55750 AGK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110245 cataract 38 HGNC:21869 Homo sapiens (human) 55750 AGK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2748 glycogen storage disease III HGNC:321 Homo sapiens (human) 178 AGL inference by association of genotype from phenotype used in manual assertion
  • PMID:16705713
  • RGD:7240710
DOID:0050741 alcohol dependence HGNC:3262 Homo sapiens (human) 26523 AGO1 inference by association of genotype from phenotype used in manual assertion
  • PMID:25495208
DOID:0050741 alcohol dependence HGNC:3263 Homo sapiens (human) 27161 AGO2 inference by association of genotype from phenotype used in manual assertion
  • PMID:25495208
DOID:1686 glaucoma HGNC:3263 Homo sapiens (human) 27161 AGO2 mutant phenotype evidence used in manual assertion
  • PMID:29392316
DOID:811 lipodystrophy HGNC:325 Homo sapiens (human) 10555 AGPAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:11967537
DOID:0111135 congenital generalized lipodystrophy type 1 HGNC:325 Homo sapiens (human) 10555 AGPAT2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110853 rhizomelic chondrodysplasia punctata type 3 HGNC:327 Homo sapiens (human) 8540 AGPS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2580 rhizomelic chondrodysplasia punctata HGNC:327 Homo sapiens (human) 8540 AGPS direct assay evidence used in manual assertion
  • PMID:9553082
DOID:0110657 congenital myasthenic syndrome 8 HGNC:329 Homo sapiens (human) 375790 AGRN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11396 pulmonary edema HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:21393362
DOID:0050589 inflammatory bowel disease HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:20717043
DOID:11123 IgA vasculitis HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:16521052
  • PMID:20702504
DOID:10763 hypertension HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:1394429
  • PMID:16739866
  • PMID:17161775
  • PMID:17334527
  • PMID:21312059
DOID:1205 allergic disease HGNC:333 Homo sapiens (human) 183 AGT inference by association of genotype from phenotype used in manual assertion
  • PMID:10200023
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 8, 2025