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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 69101 - 69125 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:3071 gliosarcoma HGNC:9604 Homo sapiens (human) 5742 PTGS1
  • MGI:6194238
DOID:1682 congenital heart disease HGNC:16867 Homo sapiens (human) 9810 RNF40
  • MGI:6194238
DOID:1558 angioedema RGD:735225 Rattus norvegicus (Norway rat) 295703 Serping1
  • MGI:6194238
DOID:1793 pancreatic cancer SGD:S000004197 Saccharomyces cerevisiae S288C 850904 HRD3
  • MGI:6194238
DOID:1793 pancreatic cancer HGNC:2593 Homo sapiens (human) 1586 CYP17A1
  • PMID:19642097
DOID:4467 clear cell renal cell carcinoma RGD:3283 Rattus norvegicus (Norway rat) 24628 Pdgfb
  • MGI:6194238
DOID:162 cancer HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • MGI:6194238
DOID:0050745 diffuse large B-cell lymphoma MGI:88336 Mus musculus (house mouse) 21939 Cd40
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:399 Homo sapiens (human) 213 ALB
  • PMID:22158777
DOID:12849 autistic disorder RGD:2650 Rattus norvegicus (Norway rat) 25451 Gabrb2
  • MGI:6194238
DOID:6432 pulmonary hypertension RGD:708528 Rattus norvegicus (Norway rat) 282821 Has1
  • PMID:19915162
DOID:2340 craniosynostosis RGD:2611 Rattus norvegicus (Norway rat) 25022 Fgfr2
  • MGI:6194238
DOID:898 autosomal dominant polycystic kidney disease HGNC:19351 Homo sapiens (human) 80114 BICC1
  • MGI:6194238
DOID:2377 multiple sclerosis MGI:98389 Mus musculus (house mouse) 20750 Spp1
  • MGI:6194238
DOID:1240 leukemia HGNC:24948 Homo sapiens (human) 84444 DOT1L
  • MGI:6194238
DOID:784 chronic kidney disease HGNC:10938 Homo sapiens (human) 10560 SLC19A2
  • MGI:6194238
DOID:0060419 chromosome 3q29 microdeletion syndrome RGD:620131 Rattus norvegicus (Norway rat) 117099 Bdh1
  • MGI:6194238
DOID:0060211 amyotrophic lateral sclerosis type 20 MGI:104820 Mus musculus (house mouse) 15382 Hnrnpa1
  • MGI:6194238
DOID:0050742 nicotine dependence WB:WBGene00022675 Caenorhabditis elegans 191240 gbb-2
  • MGI:6194238
DOID:162 cancer WB:WBGene00006894 Caenorhabditis elegans 175182 ver-1
  • MGI:6194238
DOID:0110389 retinitis pigmentosa 73 MGI:1196297 Mus musculus (house mouse) 52120 Hgsnat
  • MGI:6194238
DOID:5844 myocardial infarction MGI:106915 Mus musculus (house mouse) 22334 Vdac2
  • MGI:6194238
DOID:399 tuberculosis SGD:S000004024 Saccharomyces cerevisiae S288C 850721 SMF3
  • MGI:6194238
DOID:1059 intellectual disability MGI:1916812 Mus musculus (house mouse) 69562 Cdk13
  • MGI:6194238
DOID:0050861 colorectal adenocarcinoma HGNC:6204 Homo sapiens (human) 3725 JUN
  • PMID:8264230

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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