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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 1076 - 1100 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:10003 sensorineural hearing loss HGNC:7595 Homo sapiens (human) 4640 MYO1A inference by association of genotype from phenotype used in manual assertion
  • PMID:12736868
DOID:1380 endometrial cancer HGNC:7230 Homo sapiens (human) 4361 MRE11 inference by association of genotype from phenotype used in manual assertion
  • PMID:15048091
DOID:0050951 hereditary ataxia FB:FBgn0029943 Drosophila melanogaster (fruit fly) 31666 Atg5 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:26812546
DOID:1826 epilepsy HGNC:2295 Homo sapiens (human) 1356 CP inference by association of genotype from phenotype used in manual assertion
  • PMID:7914452
DOID:10652 Alzheimer's disease HGNC:6692 Homo sapiens (human) 4035 LRP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9635959
DOID:10155 intestinal cancer FB:FBgn0004647 Drosophila melanogaster (fruit fly) 31293 N CG3936 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:26005834
  • PMID:27680705
  • PMID:33360688
  • PMID:36400783
DOID:0060250 idiopathic scoliosis MGI:1927235 Mus musculus (house mouse) 56453 Mbtps1 author statement supported by traceable reference
  • PMID:29437042
DOID:4450 renal cell carcinoma HGNC:6720 Homo sapiens (human) 4057 LTF direct assay evidence used in manual assertion
  • PMID:23201854
DOID:0081236 autosomal recessive intellectual developmental disorder 77 HGNC:24866 Homo sapiens (human) 9731 CEP104 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110977 brachydactyly type A1C MGI:95688 Mus musculus (house mouse) 14563 Gdf5 author statement supported by traceable reference
  • MGI:5509308
DOID:0081317 multiple synostoses syndrome 1 HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:10080184
  • PMID:16151340
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:6554 Homo sapiens (human) 3953 LEPR inference by association of genotype from phenotype used in manual assertion
  • PMID:27257426
DOID:2340 craniosynostosis HGNC:3690 Homo sapiens (human) 2261 FGFR3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11467490
DOID:0110484 autosomal recessive nonsyndromic deafness 26 HGNC:4066 Homo sapiens (human) 2549 GAB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10763 hypertension RGD:620218 Rattus norvegicus (Norway rat) 81646 Creb1 direct assay evidence used in manual assertion
  • PMID:21697807
DOID:0080179 haemophilus meningitis HGNC:3616 Homo sapiens (human) 2212 FCGR2A inference by association of genotype from phenotype used in manual assertion
  • PMID:8648541
DOID:0050661 vitelliform macular dystrophy MGI:3044955 Mus musculus (house mouse) 224224 Impg2 author statement supported by traceable reference
  • PMID:32265257
DOID:0110749 type 1 diabetes mellitus 10 HGNC:6008 Homo sapiens (human) 3559 IL2RA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111308 familial febrile seizures 11 HGNC:17245 Homo sapiens (human) 57094 CPA6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110272 cataract 40 HGNC:7820 Homo sapiens (human) 4810 NHS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080187 chronic neutrophilic leukemia HGNC:2439 Homo sapiens (human) 1441 CSF3R inference by association of genotype from phenotype used in manual assertion
  • PMID:23604229
DOID:11713 diabetic angiopathy HGNC:12680 Homo sapiens (human) 7422 VEGFA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1927 sphingolipidosis FB:FBgn0086676 Drosophila melanogaster (fruit fly) 45380 spin combinatorial experimental and author inference evidence used in manual assertion
  • PMID:29046397
DOID:809 cocaine abuse WB:WBGene00000295 Caenorhabditis elegans 180837 cat-1 combinatorial experimental and author inference evidence used in manual assertion
  • PMID:22642886
DOID:684 hepatocellular carcinoma HGNC:18505 Homo sapiens (human) 54894 RNF43 mutant phenotype evidence used in manual assertion
  • PMID:23136185
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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