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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 8726 - 8750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3525 middle cerebral artery infarction HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:12675919
DOID:8725 vascular dementia HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:1824 status epilepticus HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:3312 bipolar disorder HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:16397405
  • PMID:17357145
DOID:10763 hypertension HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:0050850 diabetic encephalopathy HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
  • PMID:19154537
  • PMID:24101602
DOID:5419 schizophrenia HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
  • PMID:14745448
  • PMID:15254796
  • PMID:16397405
DOID:0050861 colorectal adenocarcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21609933
DOID:14330 Parkinson's disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:114 heart disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
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: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

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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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