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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 9901 - 9925 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:83 cataract HGNC:7782 Homo sapiens (human) 4780 NFE2L2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20064547
DOID:684 hepatocellular carcinoma HGNC:7782 Homo sapiens (human) 4780 NFE2L2 direct assay evidence used in manual assertion
  • PMID:31546024
DOID:4448 macular degeneration HGNC:7782 Homo sapiens (human) 4780 NFE2L2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23276910
DOID:0060409 NFIA-related disorder HGNC:7784 Homo sapiens (human) 4774 NFIA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050858 Marshall-Smith syndrome HGNC:7788 Homo sapiens (human) 4784 NFIX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112102 Sotos syndrome 2 HGNC:7788 Homo sapiens (human) 4784 NFIX inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10283 prostate cancer HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:26068031
  • PMID:26788504
  • PMID:28797847
DOID:3908 lung non-small cell carcinoma HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:26221384
DOID:1612 breast cancer HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28797847
DOID:0081154 common variable immunodeficiency 12 HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19797428
DOID:321 HTLV-1-associated myelopathy/tropical spastic paraparesis HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22170554
DOID:1909 melanoma HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17492467
DOID:0081152 common variable immunodeficiency 10 HGNC:7795 Homo sapiens (human) 4791 NFKB2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5684 spondyloepimetaphyseal dysplasia, Sponastrime type HGNC:7801 Homo sapiens (human) 4796 TONSL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070355 overactive bladder syndrome HGNC:7808 Homo sapiens (human) 4803 NGF direct assay evidence used in manual assertion
  • PMID:17050722
DOID:9976 heroin dependence HGNC:7808 Homo sapiens (human) 4803 NGF inference by association of genotype from phenotype used in manual assertion
  • PMID:21358750
DOID:13949 interstitial cystitis HGNC:7808 Homo sapiens (human) 4803 NGF direct assay evidence used in manual assertion
  • PMID:20227820
DOID:2986 IgA glomerulonephritis HGNC:7808 Homo sapiens (human) 4803 NGF inference by association of genotype from phenotype used in manual assertion
  • PMID:21178826
DOID:3312 bipolar disorder HGNC:7808 Homo sapiens (human) 4803 NGF inference by association of genotype from phenotype used in manual assertion
  • PMID:21294249
DOID:2841 asthma HGNC:7808 Homo sapiens (human) 4803 NGF direct assay evidence used in manual assertion
  • PMID:11737043
DOID:0060001 withdrawal disorder HGNC:7808 Homo sapiens (human) 4803 NGF direct assay evidence used in manual assertion
  • PMID:21392176
DOID:783 end stage renal disease HGNC:7808 Homo sapiens (human) 4803 NGF direct assay evidence used in manual assertion
  • PMID:19169037
DOID:0070145 hereditary sensory and autonomic neuropathy type 5 HGNC:7808 Homo sapiens (human) 4803 NGF inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2559 opiate dependence HGNC:7808 Homo sapiens (human) 4803 NGF direct assay evidence used in manual assertion
  • PMID:29224006

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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