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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 10051 - 10075 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:9252 amino acid metabolic disorder HGNC:8923 Homo sapiens (human) 26227 PHGDH inference by association of genotype from phenotype used in manual assertion
  • PMID:11055895
DOID:0080076 Neu-Laxova syndrome 1 HGNC:8923 Homo sapiens (human) 26227 PHGDH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050722 PHGDH deficiency HGNC:8923 Homo sapiens (human) 26227 PHGDH inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2747 glycogen storage disease HGNC:8925 Homo sapiens (human) 5255 PHKA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12825073
DOID:0111040 glycogen storage disease IXd HGNC:8925 Homo sapiens (human) 5255 PHKA1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111042 glycogen storage disease IXa HGNC:8926 Homo sapiens (human) 5256 PHKA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:28283841
  • PMID:28627441
  • PMID:8733134
  • RGD:7240710
DOID:2747 glycogen storage disease HGNC:8926 Homo sapiens (human) 5256 PHKA2 inference by association of genotype from phenotype used in manual assertion
  • PMID:7711737
DOID:0111041 glycogen storage disease IXb HGNC:8927 Homo sapiens (human) 5257 PHKB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111043 glycogen storage disease IXc HGNC:8931 Homo sapiens (human) 5261 PHKG2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:5082 liver cirrhosis HGNC:8931 Homo sapiens (human) 5261 PHKG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:9384616
DOID:2747 glycogen storage disease HGNC:8931 Homo sapiens (human) 5261 PHKG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:8896567
DOID:12347 osteogenesis imperfecta HGNC:23697 Homo sapiens (human) 23187 PHLDB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4440 seminoma SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:0080001 bone disease SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:10573 osteomalacia SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:3301 gonadoblastoma SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:182 calcinosis SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:3304 germinoma SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:11383 cryptorchidism SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:2994 germ cell cancer SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:3308 embryonal carcinoma SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:305 carcinoma SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:14213 hypophosphatasia SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:13994 cleidocranial dysplasia SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
DOID:3594 choriocarcinoma SGD:S000002889 Saccharomyces cerevisiae S288C 852092 PHO8 sequence similarity evidence used in manual assertion
  • PMID:25860149
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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