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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 July 29, 2024
Displaying entries 3451 - 3475 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:3526 cerebral infarction HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:17122425
  • PMID:20946167
  • PMID:25126700
DOID:0050860 colorectal adenoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:30469315
DOID:3572 intracranial sinus thrombosis HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:20946167
DOID:12336 male infertility HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:6713 cerebrovascular disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:34869693
DOID:1936 atherosclerosis HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:1287 cardiovascular system disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:18941641
  • PMID:22719980
  • PMID:24819036
  • PMID:27609361
DOID:11446 sciatic neuropathy HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:9206 Barrett's esophagus HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:18664505
DOID:11612 polycystic ovary syndrome HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:25333265
  • PMID:25445749
  • PMID:27570561
DOID:9744 type 1 diabetes mellitus HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:16489975
DOID:3393 coronary artery disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:21679057
DOID:5041 esophageal cancer HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:33292587
DOID:9538 multiple myeloma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:23699600
DOID:3910 lung adenocarcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:23374247
DOID:1682 congenital heart disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:26612412
DOID:4914 esophagus adenocarcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:22715394
DOID:850 lung disease HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:0060901 lymphoplasmacytic lymphoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:32763516
DOID:418 systemic scleroderma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:32630589
DOID:12858 Huntington's disease HGNC:4558 Homo sapiens (human) 257202 GPX6
  • PMID:18588971
DOID:7941 Barrett's adenocarcinoma HGNC:4559 Homo sapiens (human) 2882 GPX7
  • PMID:18664505
DOID:9206 Barrett's esophagus HGNC:4559 Homo sapiens (human) 2882 GPX7
  • PMID:18664505
DOID:0111671 primary hyperoxaluria type 2 HGNC:4570 Homo sapiens (human) 9380 GRHPR
  • MGI:6194238
  • RGD:7240710

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024