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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 351 - 375 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050589 inflammatory bowel disease HGNC:914 Homo sapiens (human) 567 B2M mutant phenotype evidence used in manual assertion
  • PMID:20015205
DOID:0050589 inflammatory bowel disease HGNC:11766 Homo sapiens (human) 7040 TGFB1 direct assay evidence used in manual assertion
  • PMID:28891831
DOID:0050589 inflammatory bowel disease MGI:96549 Mus musculus (house mouse) 16184 Il2ra author statement supported by traceable reference
  • PMID:7584142
DOID:0050589 inflammatory bowel disease HGNC:5344 Homo sapiens (human) 3383 ICAM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15638228
DOID:0050590 severe congenital neutropenia HGNC:2439 Homo sapiens (human) 1441 CSF3R inference by association of genotype from phenotype used in manual assertion
  • PMID:16985178
DOID:0050590 severe congenital neutropenia HGNC:3309 Homo sapiens (human) 1991 ELANE inference by association of genotype from phenotype used in manual assertion
  • PMID:10581030
  • PMID:21425445
  • PMID:24616599
DOID:0050591 tooth agenesis HGNC:12775 Homo sapiens (human) 7480 WNT10B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050591 tooth agenesis HGNC:17655 Homo sapiens (human) 64388 GREM2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050591 tooth agenesis HGNC:1071 Homo sapiens (human) 652 BMP4 inference by association of genotype from phenotype used in manual assertion
  • PMID:23079991
  • PMID:26166641
DOID:0050591 tooth agenesis HGNC:6698 Homo sapiens (human) 4040 LRP6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050591 tooth agenesis HGNC:13829 Homo sapiens (human) 80326 WNT10A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050591 tooth agenesis HGNC:1268 Homo sapiens (human) 54084 TSPEAR inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050591 tooth agenesis HGNC:3157 Homo sapiens (human) 1896 EDA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050591 tooth agenesis HGNC:1069 Homo sapiens (human) 650 BMP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23079991
DOID:0050592 asphyxiating thoracic dystrophy HGNC:7744 Homo sapiens (human) 4750 NEK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21211617
  • PMID:22499340
DOID:0050592 asphyxiating thoracic dystrophy HGNC:2962 Homo sapiens (human) 79659 DYNC2H1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22499340
DOID:0050592 asphyxiating thoracic dystrophy HGNC:29239 Homo sapiens (human) 27152 INTU inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050598 extrapulmonary tuberculosis HGNC:1641 Homo sapiens (human) 30835 CD209 inference by association of genotype from phenotype used in manual assertion
  • PMID:24874302
DOID:0050598 extrapulmonary tuberculosis HGNC:13523 Homo sapiens (human) 10332 CLEC4M inference by association of genotype from phenotype used in manual assertion
  • PMID:24874302
DOID:0050598 extrapulmonary tuberculosis HGNC:3443 Homo sapiens (human) 2069 EREG inference by association of genotype from phenotype used in manual assertion
  • PMID:30634928
DOID:0050600 ABCD syndrome HGNC:3180 Homo sapiens (human) 1910 EDNRB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050602 triple-A syndrome HGNC:13666 Homo sapiens (human) 8086 AAAS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050604 acrocapitofemoral dysplasia HGNC:5956 Homo sapiens (human) 3549 IHH inference by association of genotype from phenotype used in manual assertion
  • PMID:12632327
  • RGD:7240710
DOID:0050605 acrodermatitis enteropathica MGI:1919277 Mus musculus (house mouse) 72027 Slc39a4 author statement supported by traceable reference
  • PMID:22737083
DOID:0050605 acrodermatitis enteropathica HGNC:17129 Homo sapiens (human) 55630 SLC39A4 inference by association of genotype from phenotype used in manual assertion
  • PMID:12068297
  • RGD:7240710
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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