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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 October 9, 2024
Displaying entries 70351 - 70375 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:11247 disseminated intravascular coagulation WB:WBGene00005647 Caenorhabditis elegans 179125 srp-6
  • MGI:6194238
DOID:6432 pulmonary hypertension WB:WBGene00005647 Caenorhabditis elegans 179125 srp-6
  • MGI:6194238
DOID:0060479 Shwachman-Diamond syndrome WB:WBGene00005647 Caenorhabditis elegans 179125 srp-6
  • MGI:6194238
DOID:2841 asthma WB:WBGene00005647 Caenorhabditis elegans 179125 srp-6
  • MGI:6194238
DOID:8398 osteoarthritis WB:WBGene00005647 Caenorhabditis elegans 179125 srp-6
  • MGI:6194238
DOID:576 proteinuria WB:WBGene00005647 Caenorhabditis elegans 179125 srp-6
  • MGI:6194238
DOID:576 proteinuria WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:10952 nephritis WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:10159 osteonecrosis WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:4989 pancreatitis WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:3021 acute kidney failure WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:14115 toxic shock syndrome WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:13141 uveitis WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:0110536 autosomal recessive nonsyndromic deafness 91 WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:0050831 familial encephalopathy with neuroserpin inclusion bodies WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:3755 antithrombin III deficiency WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:2913 acute pancreatitis WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:446 primary hyperaldosteronism WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:2841 asthma WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:1184 nephrotic syndrome WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:11247 disseminated intravascular coagulation WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:11394 adult respiratory distress syndrome WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:8805 intermediate coronary syndrome WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238
DOID:2986 IgA glomerulonephritis WB:WBGene00005648 Caenorhabditis elegans 179195 srp-7
  • MGI:6194238

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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: December 9, 2024