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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 501 - 525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:0050855 renal fibrosis HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • PMID:22260463
DOID:9352 type 2 diabetes mellitus HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22399516
DOID:10283 prostate cancer HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:19851870
DOID:219 colon cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:11054 urinary bladder cancer RGD:2796 Rattus norvegicus (Norway rat) 25058 Hk1
  • PMID:23893687
DOID:0050625 biliary tract benign neoplasm HGNC:7413 Homo sapiens (human) 4507 MTAP
  • PMID:16373701
DOID:418 systemic scleroderma HGNC:543 Homo sapiens (human) 308 ANXA5
  • PMID:21124692
DOID:1168 familial hyperlipidemia RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • PMID:10892340
DOID:332 amyotrophic lateral sclerosis HGNC:4616 Homo sapiens (human) 2931 GSK3A
  • PMID:12675919
DOID:1909 melanoma HGNC:1516 Homo sapiens (human) 847 CAT
  • PMID:9758419
DOID:2349 arteriosclerosis HGNC:405 Homo sapiens (human) 218 ALDH3A1
  • PMID:3949078
DOID:13810 familial hypercholesterolemia RGD:70893 Rattus norvegicus (Norway rat) 79223 Gk
  • PMID:10642898
DOID:5419 schizophrenia HGNC:4093 Homo sapiens (human) 2572 GAD2
  • PMID:21250934
DOID:1793 pancreatic cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:6000 congestive heart failure RGD:619719 Rattus norvegicus (Norway rat) 81829 Mdh2
  • PMID:16786185
DOID:4989 pancreatitis RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • PMID:16183055
DOID:8947 diabetic retinopathy HGNC:6081 Homo sapiens (human) 3630 INS
  • PMID:22046295
DOID:4195 hyperglycemia RGD:61800 Rattus norvegicus (Norway rat) 29595 Htr2a
  • PMID:9128844
DOID:11981 morbid obesity HGNC:18129 Homo sapiens (human) 51738 GHRL
  • PMID:19188925
DOID:1074 kidney failure RGD:620396 Rattus norvegicus (Norway rat) 83504 Kl
  • PMID:10892340
DOID:583 hemolytic anemia HGNC:79 Homo sapiens (human) 28 ABO
  • PMID:3136561
DOID:0080855 Parkinsonism RGD:620103 Rattus norvegicus (Norway rat) 64639 Bad
  • PMID:23251488
DOID:12930 dilated cardiomyopathy RGD:620925 Rattus norvegicus (Norway rat) 83516 Ppargc1a
  • PMID:19242323
DOID:2580 rhizomelic chondrodysplasia punctata HGNC:327 Homo sapiens (human) 8540 AGPS
  • PMID:9553082
DOID:2316 brain ischemia RGD:619719 Rattus norvegicus (Norway rat) 81829 Mdh2
  • PMID:6282622

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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