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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 66001 - 66025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References ▲
DOID:8552 chronic myeloid leukemia HGNC:4553 Homo sapiens (human) 2876 GPX1
  • PMID:25436036
DOID:9206 Barrett's esophagus HGNC:3823 Homo sapiens (human) 27086 FOXP1
  • PMID:25447851
DOID:3070 high grade glioma HGNC:18039 Homo sapiens (human) 10765 KDM5B
  • PMID:25450384
DOID:0050933 ovarian serous carcinoma HGNC:7656 Homo sapiens (human) 4684 NCAM1
  • PMID:25455994
DOID:9279 hyperhomocysteinemia RGD:2738 Rattus norvegicus (Norway rat) 24410 Grin2b
  • PMID:25457025
DOID:9279 hyperhomocysteinemia RGD:2737 Rattus norvegicus (Norway rat) 24409 Grin2a
  • PMID:25457025
DOID:9279 hyperhomocysteinemia RGD:621531 Rattus norvegicus (Norway rat) 50592 Gria1
  • PMID:25457025
DOID:1824 status epilepticus RGD:61862 Rattus norvegicus (Norway rat) 29627 Gria2
  • PMID:25457025
DOID:1824 status epilepticus RGD:2736 Rattus norvegicus (Norway rat) 24408 Grin1
  • PMID:25457025
DOID:1824 status epilepticus RGD:2737 Rattus norvegicus (Norway rat) 24409 Grin2a
  • PMID:25457025
DOID:1273 respiratory syncytial virus infectious disease HGNC:8760 Homo sapiens (human) 5133 PDCD1
  • PMID:25465101
DOID:3627 aortic aneurysm HGNC:11255 Homo sapiens (human) 6696 SPP1
  • PMID:25465469
DOID:0060041 autism spectrum disorder HGNC:7176 Homo sapiens (human) 4318 MMP9
  • PMID:25466251
DOID:14261 fragile X syndrome HGNC:7176 Homo sapiens (human) 4318 MMP9
  • PMID:25466251
DOID:0050820 atrioventricular block HGNC:6636 Homo sapiens (human) 4000 LMNA
  • PMID:25469153
DOID:14330 Parkinson's disease WB:WBGene00002048 Caenorhabditis elegans 175807 ida-1
  • PMID:25469508
DOID:9351 diabetes mellitus WB:WBGene00002048 Caenorhabditis elegans 175807 ida-1
  • PMID:25469508
DOID:1324 lung cancer HGNC:6997 Homo sapiens (human) 4209 MEF2D
  • PMID:25472877
DOID:1984 rectal benign neoplasm HGNC:8976 Homo sapiens (human) 5291 PIK3CB
  • PMID:25473181
DOID:684 hepatocellular carcinoma RGD:621871 Rattus norvegicus (Norway rat) 26195 COX1
  • PMID:2548155
DOID:684 hepatocellular carcinoma RGD:621871 Rattus norvegicus (Norway rat) 26195 Mt-co1
  • PMID:2548155
DOID:10534 stomach cancer HGNC:3818 Homo sapiens (human) 2305 FOXM1
  • PMID:25482013
DOID:4448 macular degeneration RGD:2414 Rattus norvegicus (Norway rat) 25420 Cryab
  • PMID:25483086
DOID:13608 biliary atresia HGNC:9588 Homo sapiens (human) 5728 PTEN
  • PMID:25487473
DOID:0050328 congenital hypothyroidism MGI:98824 Mus musculus (house mouse) 22045 Trhr
  • PMID:25490146

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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