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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 10726 - 10750 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:2841 asthma HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:15741437
  • PMID:15940135
  • PMID:16387800
  • PMID:18312481
  • PMID:19096003
DOID:4483 rhinitis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:16950285
  • PMID:20109306
DOID:3393 coronary artery disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18157711
DOID:2957 pulmonary tuberculosis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18008256
DOID:3407 carotid artery disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:15640605
  • PMID:16873708
DOID:552 pneumonia HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20302606
DOID:2986 IgA glomerulonephritis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:12566518
DOID:1205 allergic disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:19222419
DOID:13580 cholestasis HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:10608 celiac disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:18728522
DOID:2945 severe acute respiratory syndrome HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:19635508
DOID:11335 sarcoidosis HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20430603
DOID:5844 myocardial infarction HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:10195920
  • PMID:14587643
  • PMID:17436151
DOID:9744 type 1 diabetes mellitus HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:10831941
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320
DOID:10487 Hirschsprung's disease HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:824 periodontitis HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:1628 Homo sapiens (human) 929 CD14
  • PMID:20555320
DOID:13603 obstructive jaundice HGNC:1628 Homo sapiens (human) 929 CD14
  • MGI:6194238
DOID:0070267 congenital disorder of glycosylation type IIo HGNC:28178 Homo sapiens (human) 84317 CCDC115
  • RGD:7240710
DOID:10783 methemoglobinemia SGD:S000001305 Saccharomyces cerevisiae S288C 854768 CBR1
  • MGI:6194238
DOID:0060076 estrogen-receptor negative breast cancer SGD:S000001305 Saccharomyces cerevisiae S288C 854768 CBR1
  • MGI:6194238
DOID:1612 breast cancer SGD:S000001305 Saccharomyces cerevisiae S288C 854768 CBR1
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:1548 Homo sapiens (human) 873 CBR1
  • MGI:6194238
DOID:1459 hypothyroidism HGNC:1516 Homo sapiens (human) 847 CAT
  • MGI:6194238

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Acknowledgements

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