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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 6126 - 6150 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:3083 chronic obstructive pulmonary disease HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:18579366
DOID:3021 acute kidney failure HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:16259926
  • PMID:16763508
DOID:0060645 chronic recurrent multifocal osteomyelitis HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4450 renal cell carcinoma HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:17031403
DOID:10247 pleurisy HGNC:6000 Homo sapiens (human) 3557 IL1RN direct assay evidence used in manual assertion
  • PMID:8491511
DOID:783 end stage renal disease HGNC:6000 Homo sapiens (human) 3557 IL1RN inference by association of genotype from phenotype used in manual assertion
  • PMID:12837270
  • PMID:16766392
  • PMID:17224277
  • PMID:20551628
DOID:5844 myocardial infarction HGNC:600 Homo sapiens (human) 335 APOA1 direct assay evidence used in manual assertion
  • PMID:20176799
DOID:9074 systemic lupus erythematosus HGNC:600 Homo sapiens (human) 335 APOA1 direct assay evidence used in manual assertion
  • PMID:20131231
DOID:13810 familial hypercholesterolemia HGNC:600 Homo sapiens (human) 335 APOA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9699897
DOID:10652 Alzheimer's disease HGNC:600 Homo sapiens (human) 335 APOA1 mutant phenotype evidence used in manual assertion
  • PMID:20847045
DOID:1387 hypolipoproteinemia HGNC:600 Homo sapiens (human) 335 APOA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:9931341
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:600 Homo sapiens (human) 335 APOA1 mutant phenotype evidence used in manual assertion
  • PMID:24793484
DOID:0080958 primary hypoalphalipoproteinemia 2 HGNC:600 Homo sapiens (human) 335 APOA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1936 atherosclerosis HGNC:600 Homo sapiens (human) 335 APOA1 direct assay evidence used in manual assertion
  • PMID:18287885
DOID:12930 dilated cardiomyopathy HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • PMID:15034580
DOID:0070600 intellectual disability and myopathy syndrome HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110451 dilated cardiomyopathy 1O HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050650 familial atrial fibrillation HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060569 hypertrichotic osteochondrodysplasia Cantu type HGNC:60 Homo sapiens (human) 10060 ABCC9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:5998 Homo sapiens (human) 9173 IL1RL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:20602249
DOID:2841 asthma HGNC:5998 Homo sapiens (human) 9173 IL1RL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19198610
  • PMID:19852851
  • PMID:21150878
  • PMID:21281963
DOID:1059 intellectual disability HGNC:5996 Homo sapiens (human) 11141 IL1RAPL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16470793
DOID:0112022 non-syndromic X-linked intellectual disability 21 HGNC:5996 Homo sapiens (human) 11141 IL1RAPL1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5041 esophageal cancer HGNC:5994 Homo sapiens (human) 7850 IL1R2 inference by association of genotype from phenotype used in manual assertion
  • PMID:31744444
DOID:1474 aggressive periodontitis HGNC:5994 Homo sapiens (human) 7850 IL1R2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24818754
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International Collaboration

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