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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:0050650 familial atrial fibrillation HGNC:7939 Homo sapiens (human) 4878 NPPA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:7939 Homo sapiens (human) 4878 NPPA inference by association of genotype from phenotype used in manual assertion
  • PMID:12514664
  • PMID:22170009
DOID:5844 myocardial infarction HGNC:7939 Homo sapiens (human) 4878 NPPA inference by association of genotype from phenotype used in manual assertion
  • PMID:12514664
DOID:0080663 atrial standstill 2 HGNC:7939 Homo sapiens (human) 4878 NPPA inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:653 purine-pyrimidine metabolic disorder HGNC:794 Homo sapiens (human) 471 ATIC inference by association of genotype from phenotype used in manual assertion
  • PMID:15114530
DOID:1936 atherosclerosis HGNC:7940 Homo sapiens (human) 4879 NPPB inference by association of genotype from phenotype used in manual assertion
  • PMID:19413180
DOID:9970 obesity HGNC:7940 Homo sapiens (human) 4879 NPPB direct assay evidence used in manual assertion
  • PMID:21959345
DOID:9651 systolic heart failure HGNC:7940 Homo sapiens (human) 4879 NPPB direct assay evidence used in manual assertion
  • PMID:23122795
DOID:5844 myocardial infarction HGNC:7940 Homo sapiens (human) 4879 NPPB direct assay evidence used in manual assertion
  • PMID:17639095
DOID:10763 hypertension HGNC:7940 Homo sapiens (human) 4879 NPPB inference by association of genotype from phenotype used in manual assertion
  • PMID:17554401
DOID:1596 depressive disorder HGNC:7941 Homo sapiens (human) 4880 NPPC inference by association of genotype from phenotype used in manual assertion
  • PMID:35642741
DOID:10763 hypertension HGNC:7941 Homo sapiens (human) 4880 NPPC inference by association of genotype from phenotype used in manual assertion
  • PMID:12452325
DOID:5844 myocardial infarction HGNC:7943 Homo sapiens (human) 4881 NPR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:14646971
DOID:0070316 Miura type epiphyseal chondrodysplasia HGNC:7944 Homo sapiens (human) 4882 NPR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080050 acromesomelic dysplasia, Maroteaux type HGNC:7944 Homo sapiens (human) 4882 NPR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:10825 essential hypertension HGNC:7944 Homo sapiens (human) 4882 NPR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10082481
DOID:10763 hypertension HGNC:7945 Homo sapiens (human) 4883 NPR3 inference by association of genotype from phenotype used in manual assertion
  • PMID:12872042
DOID:3908 lung non-small cell carcinoma HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:17582598
DOID:9256 colorectal cancer HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:30814645
DOID:1793 pancreatic cancer HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:16520463
  • PMID:18381943
  • PMID:19147782
DOID:3969 papillary thyroid carcinoma HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:19286843
DOID:9669 senile cataract HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:29156695
DOID:14330 Parkinson's disease HGNC:795 Homo sapiens (human) 472 ATM direct assay evidence used in manual assertion
  • PMID:20502937
DOID:3907 lung squamous cell carcinoma HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:28642860
DOID:0050671 female breast cancer HGNC:795 Homo sapiens (human) 472 ATM inference by association of genotype from phenotype used in manual assertion
  • PMID:30303537

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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