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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 7951 - 7975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1596 depressive disorder HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:4616 Homo sapiens (human) 2931 GSK3A
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis HGNC:4616 Homo sapiens (human) 2931 GSK3A
  • PMID:12675919
DOID:5082 liver cirrhosis HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
  • PMID:24562544
DOID:9778 irritable bowel syndrome HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
DOID:2048 autoimmune hepatitis HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
  • PMID:20208391
DOID:6432 pulmonary hypertension HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
DOID:2055 post-traumatic stress disorder HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
DOID:11088 asphyxia neonatorum HGNC:4606 Homo sapiens (human) 2923 PDIA3
  • MGI:6194238
DOID:0111671 primary hyperoxaluria type 2 HGNC:4570 Homo sapiens (human) 9380 GRHPR
  • MGI:6194238
  • RGD:7240710
DOID:2977 primary hyperoxaluria HGNC:4570 Homo sapiens (human) 9380 GRHPR
  • PMID:10484776
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:12858 Huntington's disease HGNC:4558 Homo sapiens (human) 257202 GPX6
  • PMID:18588971
DOID:13129 severe pre-eclampsia HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:8476834
DOID:11996 spermatic cord torsion HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:9408 acute myocardial infarction HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:28374671
DOID:0050731 vitamin B12 deficiency HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:11115425
DOID:10763 hypertension HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
  • PMID:21933611
  • PMID:32034489
DOID:9352 type 2 diabetes mellitus HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:18936159
  • PMID:24102912
DOID:4948 gallbladder carcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:24167362
DOID:7941 Barrett's adenocarcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:16229808
  • PMID:18664505
DOID:224 transient cerebral ischemia HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:30098076
DOID:1596 depressive disorder HGNC:4555 Homo sapiens (human) 2878 GPX3
  • MGI:6194238
DOID:0080199 colorectal carcinoma HGNC:4555 Homo sapiens (human) 2878 GPX3
  • PMID:30469315

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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