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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 51 - 75 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:6000 congestive heart failure HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:1824 status epilepticus HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:90 degenerative disc disease HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:4480 achondroplasia HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:7148 rheumatoid arthritis HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:16507130
DOID:0112282 spondyloepiphyseal dysplasia Kimberley type HGNC:319 Homo sapiens (human) 176 ACAN
  • PMID:16080123
  • RGD:7240710
DOID:9970 obesity HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:2978 carbohydrate metabolic disorder HGNC:93 Homo sapiens (human) 38 ACAT1
  • PMID:7617578
DOID:14723 beta-ketothiolase deficiency HGNC:93 Homo sapiens (human) 38 ACAT1
  • RGD:7240710
DOID:2349 arteriosclerosis HGNC:93 Homo sapiens (human) 38 ACAT1
  • PMID:15961705
DOID:783 end stage renal disease HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:1184 nephrotic syndrome HGNC:93 Homo sapiens (human) 38 ACAT1
  • MGI:6194238
DOID:10787 premature menopause HGNC:94 Homo sapiens (human) 39 ACAT2
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:94 Homo sapiens (human) 39 ACAT2
  • PMID:16195894
DOID:2841 asthma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19383228
  • PMID:19484664
DOID:3526 cerebral infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11596779
DOID:576 proteinuria HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:10193250
DOID:3393 coronary artery disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12975417
DOID:12932 endomyocardial fibrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:9970 obesity HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:17164796
DOID:10534 stomach cancer HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17035401
DOID:0050864 non-arteritic anterior ischemic optic neuropathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:21633717
DOID:9538 multiple myeloma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22345095
DOID:1205 allergic disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:10200023
DOID:0080600 COVID-19 HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:32286246
  • PMID:32386188

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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