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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 9876 - 9900 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence References
DOID:1793 pancreatic cancer HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:19250218
DOID:1417 choroid disease HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:21357402
DOID:686 liver carcinoma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:28763918
DOID:2841 asthma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:12938145
DOID:2862 glucosephosphate dehydrogenase deficiency HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:15718915
DOID:2349 arteriosclerosis HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:16523426
DOID:3070 high grade glioma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:20406895
DOID:8893 psoriasis HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:11298547
DOID:5844 myocardial infarction HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:15466015
DOID:2043 hepatitis B HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:27644568
DOID:3234 central nervous system lymphoma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:22628023
DOID:12894 Sjogren's syndrome HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:12233881
DOID:0060901 lymphoplasmacytic lymphoma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:19573080
DOID:1474 aggressive periodontitis HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:28662328
DOID:11265 trachoma HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:11023480
  • PMID:15789056
  • PMID:17947295
DOID:1470 major depressive disorder HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:30734130
DOID:12030 panuveitis HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:21357402
DOID:9663 aphthous stomatitis HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:27266194
DOID:5082 liver cirrhosis HGNC:5962 Homo sapiens (human) 3586 IL10 inference by association of genotype from phenotype used in manual assertion
  • PMID:26909998
  • PMID:27660094
DOID:2986 IgA glomerulonephritis HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21214373
DOID:783 end stage renal disease HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23615182
DOID:0060973 WHIM syndrome 2 HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11054 urinary bladder cancer HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19252927
DOID:559 acute pyelonephritis HGNC:6027 Homo sapiens (human) 3579 CXCR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22325052
DOID:1273 respiratory syncytial virus infectious disease HGNC:6029 Homo sapiens (human) 3578 IL9 inference by association of genotype from phenotype used in manual assertion
  • PMID:20503287
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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

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

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Last updated: April 7, 2025