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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 14101 - 14125 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:3144 cutis laxa MGI:1891209 Mus musculus (house mouse) 58859 Efemp2 author statement supported by traceable reference
  • PMID:26178373
DOID:0060041 autism spectrum disorder HGNC:13759 Homo sapiens (human) 23191 CYFIP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:24442360
DOID:1184 nephrotic syndrome HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:14758530
DOID:11394 adult respiratory distress syndrome RGD:3747 Rattus norvegicus (Norway rat) 24795 Serpina3n mutant phenotype evidence used in manual assertion
  • PMID:8574716
DOID:0110751 type 1 diabetes mellitus 12 HGNC:2505 Homo sapiens (human) 1493 CTLA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease WB:WBGene00002048 Caenorhabditis elegans 175807 ida-1 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:25469508
DOID:9743 diabetic neuropathy RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:17720896
DOID:3070 high grade glioma RGD:2802 Rattus norvegicus (Norway rat) 25459 Hmgb1 mutant phenotype evidence used in manual assertion
  • PMID:10830965
DOID:0050437 Danon disease HGNC:6501 Homo sapiens (human) 3920 LAMP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10591 pre-eclampsia HGNC:11936 Homo sapiens (human) 356 FASLG inference by association of genotype from phenotype used in manual assertion
  • PMID:30066360
DOID:5419 schizophrenia HGNC:922 Homo sapiens (human) 135152 B3GAT2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20950796
DOID:5353 colonic disease HGNC:4263 Homo sapiens (human) 2690 GHR inference by association of genotype from phenotype used in manual assertion
  • PMID:19864451
DOID:8725 vascular dementia RGD:620598 Rattus norvegicus (Norway rat) 114243 Nox1 mutant phenotype evidence used in manual assertion
  • PMID:24294978
DOID:10485 esophageal atresia HGNC:30858 Homo sapiens (human) 9343 EFTUD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23188108
DOID:13564 aspergillosis HGNC:11847 Homo sapiens (human) 7096 TLR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16461792
DOID:6432 pulmonary hypertension RGD:2536 Rattus norvegicus (Norway rat) 50672 Ednrb direct assay evidence used in manual assertion
  • PMID:15243299
DOID:14004 thoracic aortic aneurysm HGNC:7176 Homo sapiens (human) 4318 MMP9 inference by association of genotype from phenotype used in manual assertion
  • PMID:16678588
DOID:0080764 hereditary diffuse gastric cancer HGNC:1748 Homo sapiens (human) 999 CDH1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13141 uveitis HGNC:11766 Homo sapiens (human) 7040 TGFB1 direct assay evidence used in manual assertion
  • PMID:9008650
DOID:1024 leprosy HGNC:6709 Homo sapiens (human) 4049 LTA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:574 peripheral nervous system disease RGD:621427 Rattus norvegicus (Norway rat) 362572 Artn mutant phenotype evidence used in manual assertion
  • PMID:18344995
DOID:0111786 frontometaphyseal dysplasia 1 HGNC:3754 Homo sapiens (human) 2316 FLNA inference by association of genotype from phenotype used in manual assertion
  • PMID:16835913
  • RGD:7240710
DOID:0080162 lupus nephritis HGNC:4883 Homo sapiens (human) 3075 CFH inference by association of genotype from phenotype used in manual assertion
  • PMID:22171659
DOID:5409 lung small cell carcinoma HGNC:28611 Homo sapiens (human) 253260 RICTOR inference by association of genotype from phenotype used in manual assertion
  • PMID:27863413
DOID:12449 aplastic anemia HGNC:9360 Homo sapiens (human) 5551 PRF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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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

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Last updated: December 8, 2025