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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 5651 - 5675 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:10652 Alzheimer's disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:23348713
  • PMID:9631454
DOID:12716 newborn respiratory distress syndrome HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:25879044
DOID:409 liver disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19467940
DOID:0050073 invasive aspergillosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17311505
DOID:10754 otitis media HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:16750996
DOID:5082 liver cirrhosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:20570631
  • PMID:26857650
DOID:13375 temporal arteritis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:12375325
DOID:14115 toxic shock syndrome HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17202308
DOID:8566 herpes simplex HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15498041
  • PMID:19480845
DOID:552 pneumonia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15249448
  • PMID:18988662
DOID:11394 adult respiratory distress syndrome HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:17133182
DOID:2799 bronchiolitis obliterans HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19104434
DOID:13378 Kawasaki disease HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15144709
DOID:853 polymyalgia rheumatica HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:12375325
DOID:13450 coccidioidomycosis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:19083122
DOID:2394 ovarian cancer HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:25038892
DOID:11650 bronchopulmonary dysplasia HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:22882323
DOID:0081219 autosomal recessive intellectual developmental disorder 57 HGNC:15505 Homo sapiens (human) 79143 MBOAT7
  • RGD:7240710
DOID:10908 hydrocephalus HGNC:15505 Homo sapiens (human) 79143 MBOAT7
  • MGI:6194238
DOID:5723 optic atrophy HGNC:29622 Homo sapiens (human) 27349 MCAT
  • RGD:7240710
DOID:14749 methylmalonic acidemia HGNC:16732 Homo sapiens (human) 84693 MCEE
  • MGI:6194238
DOID:224 transient cerebral ischemia HGNC:18451 Homo sapiens (human) 90411 MCFD2
  • MGI:6194238
DOID:6000 congestive heart failure SGD:S000001568 Saccharomyces cerevisiae S288C 853777 MDH1
  • MGI:6194238
DOID:5844 myocardial infarction SGD:S000001568 Saccharomyces cerevisiae S288C 853777 MDH1
  • MGI:6194238
DOID:0080433 developmental and epileptic encephalopathy 51 SGD:S000001568 Saccharomyces cerevisiae S288C 853777 MDH1
  • MGI:6194238
  • PMID:27989324

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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