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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 26 - 50 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0080957 primary hypoalphalipoproteinemia 1 HGNC:29 Homo sapiens (human) 19 ABCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10431236
  • RGD:7240710
DOID:1387 hypolipoproteinemia HGNC:29 Homo sapiens (human) 19 ABCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11086027
DOID:1388 Tangier disease HGNC:29 Homo sapiens (human) 19 ABCA1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10431236
  • PMID:11086027
  • RGD:7240710
DOID:0060656 autosomal recessive congenital ichthyosis 1 HGNC:14637 Homo sapiens (human) 26154 ABCA12 inference by association of genotype from phenotype used in manual assertion
  • PMID:12915478
DOID:0060713 autosomal recessive congenital ichthyosis 4B HGNC:14637 Homo sapiens (human) 26154 ABCA12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0060712 autosomal recessive congenital ichthyosis 4A HGNC:14637 Homo sapiens (human) 26154 ABCA12 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3717 gastric adenocarcinoma HGNC:14638 Homo sapiens (human) 154664 ABCA13 inference by association of genotype from phenotype used in manual assertion
  • PMID:27366209
DOID:12120 pulmonary alveolar proteinosis HGNC:33 Homo sapiens (human) 21 ABCA3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111013 cone-rod dystrophy 3 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110354 retinitis pigmentosa 19 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110015 age related macular degeneration 2 HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:22661473
DOID:8501 fundus dystrophy HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:16546111
DOID:10584 retinitis pigmentosa HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:18024811
  • PMID:9466990
DOID:4448 macular degeneration HGNC:34 Homo sapiens (human) 24 ABCA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:9295268
DOID:0111364 Alzheimer's disease 9 HGNC:37 Homo sapiens (human) 10347 ABCA7 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19470683
DOID:3602 toxic encephalopathy HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17938643
DOID:1826 epilepsy HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12686700
DOID:9952 acute lymphoblastic leukemia HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22674224
DOID:8778 Crohn's disease HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15505619
DOID:1849 cannabis dependence HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19625010
DOID:12365 malaria HGNC:40 Homo sapiens (human) 5243 ABCB1 direct assay evidence used in manual assertion
  • PMID:19331170
DOID:2917 cryoglobulinemia HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:28453396
DOID:13241 Behcet's disease HGNC:40 Homo sapiens (human) 5243 ABCB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:22705826
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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