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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:2841 asthma HGNC:6029 Homo sapiens (human) 3578 IL9 mutant phenotype evidence used in manual assertion
  • PMID:21356110
DOID:11400 pyelonephritis HGNC:6026 Homo sapiens (human) 3577 CXCR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17786197
  • PMID:22325052
DOID:526 human immunodeficiency virus infectious disease HGNC:6026 Homo sapiens (human) 3577 CXCR1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080784 urinary tract infection HGNC:6026 Homo sapiens (human) 3577 CXCR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21151974
DOID:219 colon cancer HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • PMID:29755661
DOID:10534 stomach cancer HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • PMID:18687755
DOID:612 primary immunodeficiency disease HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • PMID:19505916
DOID:627 severe combined immunodeficiency HGNC:6024 Homo sapiens (human) 3575 IL7R inference by association of genotype from phenotype used in manual assertion
  • PMID:9843216
DOID:13777 epidermodysplasia verruciformis HGNC:6023 Homo sapiens (human) 3574 IL7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:6021 Homo sapiens (human) 3572 IL6ST inference by association of genotype from phenotype used in manual assertion
  • PMID:17664290
DOID:612 primary immunodeficiency disease HGNC:6021 Homo sapiens (human) 3572 IL6ST inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080596 hyper IgE recurrent infection syndrome 4 HGNC:6021 Homo sapiens (human) 3572 IL6ST inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11613 hyperandrogenism HGNC:6021 Homo sapiens (human) 3572 IL6ST inference by association of genotype from phenotype used in manual assertion
  • PMID:12917504
DOID:10652 Alzheimer's disease HGNC:6019 Homo sapiens (human) 3570 IL6R inference by association of genotype from phenotype used in manual assertion
  • PMID:20197062
DOID:10534 stomach cancer HGNC:6019 Homo sapiens (human) 3570 IL6R inference by association of genotype from phenotype used in manual assertion
  • PMID:28442395
DOID:9970 obesity HGNC:6019 Homo sapiens (human) 3570 IL6R inference by association of genotype from phenotype used in manual assertion
  • PMID:12917504
  • PMID:16817825
  • PMID:17984249
DOID:0080545 hyper IgE syndrome HGNC:6019 Homo sapiens (human) 3570 IL6R inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12858 Huntington's disease HGNC:6019 Homo sapiens (human) 3570 IL6R mutant phenotype evidence used in manual assertion
  • PMID:11860469
DOID:10140 dry eye syndrome HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:18419107
DOID:12894 Sjogren's syndrome HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:11426023
DOID:1474 aggressive periodontitis HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:28662328
DOID:8947 diabetic retinopathy HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:19140096
  • PMID:19542902
DOID:9744 type 1 diabetes mellitus HGNC:6018 Homo sapiens (human) 3569 IL6 direct assay evidence used in manual assertion
  • PMID:19382103
DOID:1883 hepatitis C HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:28340949
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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