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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 10001 - 10025 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0110013 advanced sleep phase syndrome 3 HGNC:8847 Homo sapiens (human) 8863 PER3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081274 peroxisome biogenesis disorder 14B HGNC:8853 Homo sapiens (human) 8799 PEX11B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080487 peroxisome biogenesis disorder 13A HGNC:8856 Homo sapiens (human) 5195 PEX14 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080486 peroxisome biogenesis disorder 12A HGNC:9713 Homo sapiens (human) 5824 PEX19 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0081440 Peroxisome biogenesis disorder 10B HGNC:8858 Homo sapiens (human) 8504 PEX3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080484 peroxisome biogenesis disorder 10A HGNC:8858 Homo sapiens (human) 8504 PEX3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2747 glycogen storage disease SGD:S000003472 Saccharomyces cerevisiae S288C 853155 PFK1 sequence similarity evidence used in manual assertion
  • PMID:7825568
DOID:2747 glycogen storage disease SGD:S000003472 Saccharomyces cerevisiae S288C 853155 PFK1 genetic interaction evidence used in manual assertion
  • PMID:7825568
DOID:2747 glycogen storage disease SGD:S000004818 Saccharomyces cerevisiae S288C 855245 PFK2 genetic interaction evidence used in manual assertion
  • PMID:7825568
DOID:2747 glycogen storage disease SGD:S000004818 Saccharomyces cerevisiae S288C 855245 PFK2 sequence similarity evidence used in manual assertion
  • PMID:7825568
DOID:11721 glycogen storage disease VII HGNC:8877 Homo sapiens (human) 5213 PFKM inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11721 glycogen storage disease VII HGNC:8877 Homo sapiens (human) 5213 PFKM direct assay evidence used in manual assertion
  • PMID:1533013
DOID:0060209 amyotrophic lateral sclerosis type 18 HGNC:8881 Homo sapiens (human) 5216 PFN1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080108 myoglobinuria HGNC:8889 Homo sapiens (human) 5224 PGAM2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8447317
DOID:0070435 hyperphosphatasia with impaired intellectual development syndrome 3 HGNC:17893 Homo sapiens (human) 27315 PGAP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070436 hyperphosphatasia with impaired intellectual development syndrome 4 HGNC:23719 Homo sapiens (human) 93210 PGAP3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2841 asthma HGNC:8893 Homo sapiens (human) 5228 PGF direct assay evidence used in manual assertion
  • PMID:22268141
DOID:9743 diabetic neuropathy HGNC:8893 Homo sapiens (human) 5228 PGF mutant phenotype evidence used in manual assertion
  • PMID:21056561
DOID:5844 myocardial infarction HGNC:8893 Homo sapiens (human) 5228 PGF direct assay evidence used in manual assertion
  • PMID:22114497
DOID:2316 brain ischemia HGNC:8893 Homo sapiens (human) 5228 PGF mutant phenotype evidence used in manual assertion
  • PMID:16901914
DOID:3068 glioblastoma HGNC:8893 Homo sapiens (human) 5228 PGF direct assay evidence used in manual assertion
  • PMID:20458050
DOID:1798 pancreatic endocrine carcinoma HGNC:8893 Homo sapiens (human) 5228 PGF mutant phenotype evidence used in manual assertion
  • PMID:26861455
DOID:162 cancer SGD:S000000605 Saccharomyces cerevisiae S288C 850370 PGK1 genetic interaction evidence used in manual assertion
  • PMID:26354769
DOID:0111933 phosphoglycerate kinase 1 deficiency HGNC:8896 Homo sapiens (human) 5230 PGK1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:583 hemolytic anemia HGNC:8896 Homo sapiens (human) 5230 PGK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16740138
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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