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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 14126 - 14150 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:1064 cystinosis WB:WBGene00008052 Caenorhabditis elegans 174308 ctns-1 mutant phenotype evidence used in manual assertion
  • PMID:22822152
DOID:2986 IgA glomerulonephritis HGNC:3608 Homo sapiens (human) 2204 FCAR mutant phenotype evidence used in manual assertion
  • PMID:21985370
DOID:10286 prostate carcinoma HGNC:1733 Homo sapiens (human) 8621 CDK13 mutant phenotype evidence used in manual assertion
  • PMID:33390186
DOID:0080642 Middle East respiratory syndrome HGNC:3009 Homo sapiens (human) 1803 DPP4 mutant phenotype evidence used in manual assertion
  • PMID:30256968
  • PMID:30626685
  • PMID:31838832
DOID:576 proteinuria RGD:2070 Rattus norvegicus (Norway rat) 24180 Agtr1a mutant phenotype evidence used in manual assertion
  • PMID:20042458
DOID:1574 alcohol use disorder WB:WBGene00016872 Caenorhabditis elegans 183715 dop-4 mutant phenotype evidence used in manual assertion
  • PMID:24681782
DOID:4074 pancreatic adenocarcinoma HGNC:6840 Homo sapiens (human) 5604 MAP2K1 mutant phenotype evidence used in manual assertion
  • PMID:28849200
DOID:2030 anxiety disorder RGD:620688 Rattus norvegicus (Norway rat) 84390 Hcn1 mutant phenotype evidence used in manual assertion
  • PMID:22884333
DOID:1686 glaucoma HGNC:21205 Homo sapiens (human) 84894 LINGO1 mutant phenotype evidence used in manual assertion
  • PMID:19422885
DOID:2799 bronchiolitis obliterans RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:17097496
DOID:0050659 biotin-responsive basal ganglia disease WB:WBGene00044738 Caenorhabditis elegans 4363081 folt-3 sequence alignment evidence used in manual assertion
  • PMID:17475669
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:0050709 early infantile epileptic encephalopathy SGD:S000005662 Saccharomyces cerevisiae S288C 854303 IDH2 sequence similarity evidence used in manual assertion
  • PMID:28058510
DOID:2476 hereditary spastic paraplegia SGD:S000005691 Saccharomyces cerevisiae S288C 854336 SEY1 sequence similarity evidence used in manual assertion
  • PMID:19665976
DOID:0080563 congenital disorder of glycosylation Ik SGD:S000000314 Saccharomyces cerevisiae S288C 852407 ALG1 sequence similarity evidence used in manual assertion
  • PMID:26931382
DOID:162 cancer SGD:S000005816 Saccharomyces cerevisiae S288C 854465 SNF2 sequence similarity evidence used in manual assertion
  • PMID:30700905
DOID:219 colon cancer SGD:S000000671 Saccharomyces cerevisiae S288C 850438 ERS1 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:0060559 lethal congenital contracture syndrome 1 SGD:S000002366 Saccharomyces cerevisiae S288C 851320 GLE1 sequence similarity evidence used in manual assertion
  • PMID:24243016
DOID:162 cancer SGD:S000001518 Saccharomyces cerevisiae S288C 853830 UGP1 sequence similarity evidence used in manual assertion
  • PMID:26354769
DOID:162 cancer SGD:S000005675 Saccharomyces cerevisiae S288C 854320 SMP3 sequence similarity evidence used in manual assertion
  • PMID:26354769
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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