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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 October 9, 2024
Displaying entries 70776 - 70800 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:1485 cystic fibrosis HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:21993476
  • PMID:24127697
DOID:3083 chronic obstructive pulmonary disease HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:20133931
DOID:6432 pulmonary hypertension HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:21041689
DOID:0080162 lupus nephritis HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:22513366
DOID:224 transient cerebral ischemia HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:9540 vascular skin disease HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:11457670
DOID:7148 rheumatoid arthritis HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:20541603
DOID:10283 prostate cancer HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:15666359
DOID:5082 liver cirrhosis HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:22669512
DOID:8398 osteoarthritis HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:783 end stage renal disease HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:21822023
DOID:0050589 inflammatory bowel disease HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:21939913
DOID:5844 myocardial infarction HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:16728681
DOID:0060224 atrial fibrillation HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:21652096
DOID:3021 acute kidney failure HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:21811803
DOID:10652 Alzheimer's disease HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:22415896
  • PMID:8751438
DOID:5419 schizophrenia HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:22146151
DOID:3407 carotid artery disease HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:21906738
DOID:2316 brain ischemia HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:13564 aspergillosis HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:22114731
DOID:3770 pulmonary fibrosis HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
  • PMID:22669512
DOID:77 gastrointestinal system disease HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:1875 impotence HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:20668462
  • PMID:22337222
DOID:4676 uremia HGNC:320 Homo sapiens (human) 177 AGER
  • MGI:6194238

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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: December 9, 2024