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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 10026 - 10050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0081267 graft-versus-host disease HGNC:79 Homo sapiens (human) 28 ABO direct assay evidence used in manual assertion
  • PMID:3289150
DOID:583 hemolytic anemia HGNC:79 Homo sapiens (human) 28 ABO direct assay evidence used in manual assertion
  • PMID:3136561
DOID:1496 echinococcosis HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:2142987
DOID:1793 pancreatic cancer HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:20103627
DOID:4948 gallbladder carcinoma HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:7795450
DOID:2841 asthma HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:16008680
DOID:10763 hypertension HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:32379894
DOID:0080600 COVID-19 HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:32379894
DOID:1240 leukemia HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:18426641
DOID:14067 Plasmodium falciparum malaria HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:18003641
DOID:552 pneumonia HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:4375858
DOID:2237 hepatitis HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:32379894
DOID:13406 pulmonary sarcoidosis HGNC:79 Homo sapiens (human) 28 ABO inference by association of genotype from phenotype used in manual assertion
  • PMID:9036208
DOID:0060259 renal-hepatic-pancreatic dysplasia HGNC:7907 Homo sapiens (human) 27031 NPHP3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0070121 Meckel syndrome 7 HGNC:7907 Homo sapiens (human) 27031 NPHP3 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111114 nephronophthisis 3 HGNC:7907 Homo sapiens (human) 27031 NPHP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:12872122
  • RGD:7240710
DOID:12712 nephronophthisis HGNC:7907 Homo sapiens (human) 27031 NPHP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:17855640
DOID:10763 hypertension HGNC:7907 Homo sapiens (human) 27031 NPHP3 inference by association of genotype from phenotype used in manual assertion
  • PMID:19177160
DOID:0080390 nephrotic syndrome type 1 HGNC:7908 Homo sapiens (human) 4868 NPHS1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110009 achromatopsia 7 HGNC:791 Homo sapiens (human) 22926 ATF6 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:7910 Homo sapiens (human) 4869 NPM1 mutant phenotype evidence used in manual assertion
  • PMID:24184354
DOID:9119 acute myeloid leukemia HGNC:7910 Homo sapiens (human) 4869 NPM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15659725
  • PMID:17957027
  • RGD:7240710
DOID:9119 acute myeloid leukemia HGNC:7910 Homo sapiens (human) 4869 NPM1 direct assay evidence used in manual assertion
  • PMID:25992555
DOID:8283 peritonitis HGNC:7939 Homo sapiens (human) 4878 NPPA direct assay evidence used in manual assertion
  • PMID:23422200
DOID:1073 renal hypertension HGNC:7939 Homo sapiens (human) 4878 NPPA direct assay evidence used in manual assertion
  • PMID:15241786

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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