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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 9926 - 9950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:5844 myocardial infarction HGNC:7808 Homo sapiens (human) 4803 NGF mutant phenotype evidence used in manual assertion
  • PMID:20360245
DOID:10652 Alzheimer's disease HGNC:7809 Homo sapiens (human) 4804 NGFR inference by association of genotype from phenotype used in manual assertion
  • PMID:18780967
DOID:1596 depressive disorder HGNC:7809 Homo sapiens (human) 4804 NGFR inference by association of genotype from phenotype used in manual assertion
  • PMID:15274039
DOID:0060599 Nance-Horan syndrome HGNC:7820 Homo sapiens (human) 4810 NHS inference by association of genotype from phenotype used in manual assertion
  • PMID:16736028
  • 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:9970 obesity HGNC:7842 Homo sapiens (human) 4828 NMB inference by association of genotype from phenotype used in manual assertion
  • PMID:11194934
  • PMID:15585758
DOID:769 neuroblastoma HGNC:7849 Homo sapiens (human) 4830 NME1 inference by association of genotype from phenotype used in manual assertion
  • PMID:8047138
DOID:3307 teratoma HGNC:7849 Homo sapiens (human) 4830 NME1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7518576
DOID:2152 ovary epithelial cancer HGNC:7849 Homo sapiens (human) 4830 NME1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7622307
DOID:3307 teratoma HGNC:7850 Homo sapiens (human) 4831 NME2 inference by association of genotype from phenotype used in manual assertion
  • PMID:7518576
DOID:9970 obesity HGNC:7859 Homo sapiens (human) 10874 NMU inference by association of genotype from phenotype used in manual assertion
  • PMID:16984985
DOID:10286 prostate carcinoma HGNC:786 Homo sapiens (human) 468 ATF4 direct assay evidence used in manual assertion
  • PMID:25680860
DOID:0080620 familial glucocorticoid deficiency HGNC:7863 Homo sapiens (human) 23530 NNT inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:7865 Homo sapiens (human) 4838 NODAL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9296 cleft lip HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:25339627
  • PMID:25704602
DOID:9834 hyperopia HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:16151340
DOID:0050789 tarsal-carpal coalition syndrome HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:26211601
  • RGD:7240710
DOID:12858 Huntington's disease HGNC:7866 Homo sapiens (human) 9241 NOG mutant phenotype evidence used in manual assertion
  • PMID:17885687
DOID:0050788 proximal symphalangism HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:10080184
  • PMID:11846737
  • PMID:24326127
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:0080787 proximal symphalangism 1 HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110975 brachydactyly type B2 HGNC:7866 Homo sapiens (human) 9241 NOG inference by association of genotype from phenotype used in manual assertion
  • PMID:17668388
  • RGD:7240710
DOID:2340 craniosynostosis HGNC:7866 Homo sapiens (human) 9241 NOG direct assay evidence used in manual assertion
  • PMID:19627528
DOID:1059 intellectual disability HGNC:7871 Homo sapiens (human) 4841 NONO inference by association of genotype from phenotype used in manual assertion
  • PMID:26571461
  • PMID:36653413
DOID:0060817 syndromic X-linked intellectual disability 34 HGNC:7871 Homo sapiens (human) 4841 NONO 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.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025