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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 5926 - 5950 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:824 periodontitis HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:17209781
DOID:10763 hypertension HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:19043252
DOID:2018 hyperinsulinism HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:19375766
DOID:0060901 lymphoplasmacytic lymphoma HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:19573080
DOID:2862 glucosephosphate dehydrogenase deficiency HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:15718915
DOID:8567 Hodgkin's lymphoma HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:19573080
DOID:341 peripheral vascular disease HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:19397692
DOID:0060688 arteriovenous malformations of the brain HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9351 diabetes mellitus HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:18689695
DOID:4677 keratitis HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:22503230
DOID:10763 hypertension HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:12846758
DOID:2377 multiple sclerosis HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:24155968
DOID:9119 acute myeloid leukemia HGNC:6018 Homo sapiens (human) 3569 IL6 mutant phenotype evidence used in manual assertion
  • PMID:8892684
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:28852433
DOID:2043 hepatitis B HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:27268603
DOID:8778 Crohn's disease HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12858 Huntington's disease HGNC:6018 Homo sapiens (human) 3569 IL6 mutant phenotype evidence used in manual assertion
  • PMID:11860469
DOID:9256 colorectal cancer HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:28349833
DOID:8632 Kaposi's sarcoma HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:13141 uveitis HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:1544781
DOID:11716 prediabetes syndrome HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:19442860
DOID:9352 type 2 diabetes mellitus HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:18573122
  • PMID:28303994
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:19127455
  • RGD:7240710
DOID:10941 intracranial aneurysm HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:16648144
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:27730688

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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