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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 6576 - 6600 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▼ Evidence Code Names References
DOID:12716 newborn respiratory distress syndrome WB:WBGene00002028 Caenorhabditis elegans 177675 hst-1
  • MGI:6194238
DOID:535 sleep disorder MGI:96572 Mus musculus (house mouse) 16333 Ins1
  • MGI:6194238
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 WB:WBGene00020307 Caenorhabditis elegans 173469 T07D3.4
  • MGI:6194238
DOID:9074 systemic lupus erythematosus RGD:3038 Rattus norvegicus (Norway rat) 25478 Man2a1
  • MGI:6194238
DOID:5844 myocardial infarction SGD:S000006205 Saccharomyces cerevisiae S288C 856107 CIT3
  • MGI:6194238
DOID:12783 migraine without aura MGI:95394 Mus musculus (house mouse) 13807 Eno2
  • MGI:6194238
DOID:9266 cystinuria FB:FBgn0002571 Drosophila melanogaster (fruit fly) 35826 Mal-A3
  • MGI:6194238
DOID:0050697 chorioamnionitis HGNC:6922 Homo sapiens (human) 4153 MBL2
  • PMID:15723707
DOID:12554 hemolytic-uremic syndrome Xenbase:XB-GENE-941235 Xenopus laevis (African clawed frog) 495031 c1galt1c1.L
  • MGI:6194238
DOID:162 cancer FB:FBgn0250906 Drosophila melanogaster (fruit fly) 33461 Pgk
  • MGI:6194238
DOID:1800 neuroendocrine carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15010880
DOID:14723 beta-ketothiolase deficiency HGNC:93 Homo sapiens (human) 38 ACAT1
  • RGD:7240710
DOID:1875 impotence HGNC:936 Homo sapiens (human) 572 BAD
  • MGI:6194238
DOID:0110860 polycystic kidney disease 3 SGD:S000000433 Saccharomyces cerevisiae S288C 852530 ROT2
  • MGI:6194238
DOID:1612 breast cancer HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:22560646
DOID:2349 arteriosclerosis HGNC:11850 Homo sapiens (human) 7099 TLR4
  • PMID:16890863
DOID:3070 high grade glioma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:12540498
DOID:3770 pulmonary fibrosis HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:12030733
DOID:0050855 renal fibrosis HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • PMID:22260463
DOID:3021 acute kidney failure HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
DOID:9975 cocaine dependence HGNC:8846 Homo sapiens (human) 8864 PER2
  • PMID:22832851
DOID:11832 visual epilepsy HGNC:6257 Homo sapiens (human) 3767 KCNJ11
  • MGI:6194238
DOID:9870 galactosemia HGNC:381 Homo sapiens (human) 231 AKR1B1
  • MGI:6194238
DOID:90 degenerative disc disease HGNC:319 Homo sapiens (human) 176 ACAN
  • MGI:6194238
DOID:9120 amyloidosis MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • 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: August 19, 2024