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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 13951 - 13975 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:9744 type 1 diabetes mellitus HGNC:1603 Homo sapiens (human) 729230 CCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10400139
DOID:9744 type 1 diabetes mellitus HGNC:1667 Homo sapiens (human) 952 CD38 direct assay evidence used in manual assertion
  • PMID:12488956
  • PMID:16459468
DOID:9744 type 1 diabetes mellitus HGNC:20580 Homo sapiens (human) 120227 CYP2R1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17607662
DOID:9744 type 1 diabetes mellitus HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:19382103
DOID:9775 diastolic heart failure HGNC:2707 Homo sapiens (human) 1636 ACE inference by association of genotype from phenotype used in manual assertion
  • PMID:19021695
  • PMID:19752885
DOID:9775 diastolic heart failure RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:14757777
DOID:9775 diastolic heart failure RGD:3001 Rattus norvegicus (Norway rat) 24536 Lepr inference by association of genotype from phenotype used in manual assertion
  • PMID:33568522
DOID:9778 irritable bowel syndrome HGNC:5297 Homo sapiens (human) 3359 HTR3A inference by association of genotype from phenotype used in manual assertion
  • PMID:21420406
DOID:9778 irritable bowel syndrome RGD:3186 Rattus norvegicus (Norway rat) 24600 Nos3 direct assay evidence used in manual assertion
  • PMID:23691109
DOID:9778 irritable bowel syndrome MGI:1927999 Mus musculus (house mouse) 58805 Mlxipl author statement supported by traceable reference
  • PMID:29669261
DOID:9778 irritable bowel syndrome HGNC:18505 Homo sapiens (human) 54894 RNF43 inference by association of genotype from phenotype used in manual assertion
  • PMID:29416670
DOID:980 choroidal sclerosis HGNC:4689 Homo sapiens (human) 3000 GUCY2D inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:980 choroidal sclerosis HGNC:9942 Homo sapiens (human) 5961 PRPH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:16832026
  • PMID:8644804
  • RGD:7240710
DOID:9810 polyarteritis nodosa HGNC:3327 Homo sapiens (human) 2006 ELN direct assay evidence used in manual assertion
  • PMID:12643515
DOID:9821 choroideremia HGNC:1940 Homo sapiens (human) 1121 CHM inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9822 partial central choroid dystrophy MGI:102791 Mus musculus (house mouse) 19133 Prph2 author statement supported by traceable reference
  • PMID:37914688
DOID:9827 radioulnar synostosis HGNC:6772 Homo sapiens (human) 4091 SMAD6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9827 radioulnar synostosis HGNC:5101 Homo sapiens (human) 3207 HOXA11 inference by association of genotype from phenotype used in manual assertion
  • PMID:11101832
DOID:9828 neonatal abstinence syndrome HGNC:8154 Homo sapiens (human) 4986 OPRK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:26233486
DOID:9828 neonatal abstinence syndrome HGNC:2615 Homo sapiens (human) 1555 CYP2B6 inference by association of genotype from phenotype used in manual assertion
  • PMID:28320034
DOID:9828 neonatal abstinence syndrome HGNC:8156 Homo sapiens (human) 4988 OPRM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23632726
  • PMID:26233486
DOID:9828 neonatal abstinence syndrome HGNC:2228 Homo sapiens (human) 1312 COMT inference by association of genotype from phenotype used in manual assertion
  • PMID:23632726
  • PMID:26233486
  • PMID:27983768
DOID:9834 hyperopia HGNC:1181 Homo sapiens (human) 745 MYRF inference by association of genotype from phenotype used in manual assertion
  • PMID:36129575
DOID:9834 hyperopia HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:16151340
DOID:9849 Meniere's disease HGNC:637 Homo sapiens (human) 361 AQP4 inference by association of genotype from phenotype used in manual assertion
  • PMID:21063116
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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