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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 68601 - 68625 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:3908 lung non-small cell carcinoma HGNC:9865 Homo sapiens (human) 5915 RARB
  • PMID:18349282
  • PMID:23599765
DOID:9970 obesity RGD:70553 Rattus norvegicus (Norway rat) 113959 C5ar1
  • PMID:23118029
DOID:3454 brain infarction RGD:2794 Rattus norvegicus (Norway rat) 24446 Hgf
  • PMID:16421510
DOID:4247 coronary restenosis HGNC:11255 Homo sapiens (human) 6696 SPP1
  • PMID:16373617
DOID:8466 retinal degeneration HGNC:4893 Homo sapiens (human) 3082 HGF
  • PMID:15505072
DOID:850 lung disease RGD:2049 Rattus norvegicus (Norway rat) 25369 Adora2a
  • PMID:16484904
  • PMID:19487932
DOID:11476 osteoporosis HGNC:2561 Homo sapiens (human) 7852 CXCR4
  • PMID:29882473
DOID:2378 relapsing-remitting multiple sclerosis HGNC:2466 Homo sapiens (human) 1464 CSPG4
  • PMID:10976643
DOID:0080322 polycystic kidney disease RGD:2069 Rattus norvegicus (Norway rat) 24179 Agt
  • PMID:20798958
DOID:10763 hypertension RGD:1310740 Rattus norvegicus (Norway rat) 291437 Lipg
  • PMID:15914124
DOID:3525 middle cerebral artery infarction RGD:3285 Rattus norvegicus (Norway rat) 24629 Pdgfrb
  • PMID:16917016
DOID:3407 carotid artery disease HGNC:11290 Homo sapiens (human) 6721 SREBF2
  • PMID:12801623
DOID:2841 asthma HGNC:270 Homo sapiens (human) 142 PARP1
  • PMID:26205779
DOID:3963 thyroid gland carcinoma HGNC:855 Homo sapiens (human) 527 ATP6V0C
  • PMID:30884810
DOID:13141 uveitis HGNC:5973 Homo sapiens (human) 3596 IL13
  • PMID:11481267
  • PMID:17392164
DOID:11450 allergic cutaneous vasculitis HGNC:2438 Homo sapiens (human) 1440 CSF3
  • PMID:20100783
DOID:7442 monoclonal gammopathy of uncertain significance HGNC:7737 Homo sapiens (human) 4744 NEFH
  • PMID:12536221
DOID:14115 toxic shock syndrome HGNC:775 Homo sapiens (human) 462 SERPINC1
  • PMID:16732381
DOID:3021 acute kidney failure HGNC:320 Homo sapiens (human) 177 AGER
  • PMID:21811803
DOID:9778 irritable bowel syndrome RGD:3186 Rattus norvegicus (Norway rat) 24600 Nos3
  • PMID:23691109
DOID:5295 intestinal disease RGD:3732 Rattus norvegicus (Norway rat) 24787 Sod2
  • PMID:26301045
DOID:3500 gallbladder adenocarcinoma HGNC:2731 Homo sapiens (human) 4921 DDR2
  • PMID:29043607
DOID:1679 cystitis RGD:628641 Rattus norvegicus (Norway rat) 84023 Ptger4
  • PMID:20860016
DOID:6432 pulmonary hypertension HGNC:12726 Homo sapiens (human) 7450 VWF
  • PMID:14507115
DOID:219 colon cancer HGNC:393 Homo sapiens (human) 10000 AKT3
  • PMID:20811704

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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