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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 11051 - 11075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0050908 myelodysplastic syndrome HGNC:5382 Homo sapiens (human) 3417 IDH1
  • PMID:24936872
DOID:0050866 oral squamous cell carcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21393552
DOID:10763 hypertension HGNC:404 Homo sapiens (human) 217 ALDH2
  • PMID:11510748
  • PMID:12484509
DOID:9744 type 1 diabetes mellitus HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • PMID:17223345
  • PMID:17606874
DOID:1067 open-angle glaucoma HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:20357201
DOID:2349 arteriosclerosis HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:16458279
DOID:9352 type 2 diabetes mellitus HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:16868148
DOID:1574 alcohol use disorder HGNC:90 Homo sapiens (human) 35 ACADS
  • PMID:20554694
DOID:0110429 dilated cardiomyopathy 1H HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:20123316
DOID:9351 diabetes mellitus HGNC:4195 Homo sapiens (human) 2645 GCK
  • PMID:11372010
DOID:10783 methemoglobinemia HGNC:2873 Homo sapiens (human) 1727 CYB5R3
  • PMID:11295830
DOID:446 primary hyperaldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • PMID:1731223
DOID:8947 diabetic retinopathy HGNC:288 Homo sapiens (human) 155 ADRB3
  • PMID:9313761
DOID:12804 mucopolysaccharidosis IV HGNC:4298 Homo sapiens (human) 2720 GLB1
  • PMID:11511921
  • PMID:19091613
DOID:3211 lysosomal storage disease HGNC:318 Homo sapiens (human) 175 AGA
  • PMID:1703489
DOID:0070112 Niemann-Pick disease type B HGNC:11120 Homo sapiens (human) 6609 SMPD1
  • RGD:7240710
DOID:11713 diabetic angiopathy HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:18575614
DOID:4483 rhinitis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:16950285
  • PMID:20109306
DOID:0112303 spondylometaphyseal dysplasia with corneal dystrophy HGNC:9056 Homo sapiens (human) 5331 PLCB3
  • RGD:7240710
DOID:2394 ovarian cancer HGNC:8125 Homo sapiens (human) 4968 OGG1
  • PMID:24698998
DOID:0050860 colorectal adenoma HGNC:9603 Homo sapiens (human) 5740 PTGIS
  • PMID:16537708
DOID:552 pneumonia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:4375858
DOID:0050589 inflammatory bowel disease HGNC:5344 Homo sapiens (human) 3383 ICAM1
  • PMID:15638228
DOID:848 arthritis HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:16461442
DOID:5844 myocardial infarction HGNC:6562 Homo sapiens (human) 3957 LGALS2
  • PMID:15129282
  • RGD:7240710

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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