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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 8776 - 8800 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8805 intermediate coronary syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:11451295
  • PMID:15131005
DOID:7147 ankylosing spondylitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:22876137
DOID:10652 Alzheimer's disease HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:841 extrinsic allergic alveolitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:19218674
DOID:2799 bronchiolitis obliterans HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:8970 subacute sclerosing panencephalitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:16741935
DOID:7693 abdominal aortic aneurysm HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:25208933
DOID:3021 acute kidney failure HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:2527 nephrosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:12986 leukostasis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:12549 hepatitis A HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:12458570
DOID:3525 middle cerebral artery infarction HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:9775 diastolic heart failure HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19021695
  • PMID:19752885
DOID:14115 toxic shock syndrome HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:28336767
DOID:5082 liver cirrhosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19456900
  • PMID:26681055
  • PMID:29085215
DOID:11984 hypertrophic cardiomyopathy HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:9270088
DOID:6000 congestive heart failure HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:0050851 glomerulosclerosis HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:790 ocular hypotension HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:988 mitral valve prolapse HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:17379330
DOID:4481 allergic rhinitis HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15112973
DOID:3827 congenital diaphragmatic hernia HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:0111128 focal segmental glomerulosclerosis 1 HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
DOID:11123 Henoch-Schoenlein purpura HGNC:2707 Homo sapiens (human) 1636 ACE
  • PMID:15315169

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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