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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 69201 - 69225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence Code Names References
DOID:3498 pancreatic ductal adenocarcinoma HGNC:12705 Homo sapiens (human) 8876 VNN1
  • PMID:32663515
DOID:11612 polycystic ovary syndrome RGD:3853 Rattus norvegicus (Norway rat) 25085 Th
  • PMID:15795180
DOID:8947 diabetic retinopathy RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace
  • MGI:6194238
DOID:11981 morbid obesity MGI:2180756 Mus musculus (house mouse) 207911 Mchr1
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:21899 Homo sapiens (human) 285973 ATG9B
  • MGI:6194238
DOID:0110064 amelogenesis imperfecta type 1H MGI:96615 Mus musculus (house mouse) 16420 Itgb6
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:5021 Homo sapiens (human) 3169 FOXA1
  • PMID:25965836
  • PMID:31400761
DOID:1307 dementia HGNC:9204 Homo sapiens (human) 5444 PON1
  • PMID:15016430
DOID:1312 focal segmental glomerulosclerosis HGNC:333 Homo sapiens (human) 183 AGT
  • MGI:6194238
DOID:784 chronic kidney disease MGI:892021 Mus musculus (house mouse) 16617 Klk1b24
  • MGI:6194238
DOID:783 end stage renal disease HGNC:2201 Homo sapiens (human) 1281 COL3A1
  • PMID:19424605
DOID:1596 depressive disorder MGI:94864 Mus musculus (house mouse) 13166 Dbh
  • MGI:6194238
DOID:9970 obesity HGNC:3020 Homo sapiens (human) 1812 DRD1
  • MGI:6194238
DOID:6364 migraine HGNC:3467 Homo sapiens (human) 2099 ESR1
  • RGD:7240710
DOID:12721 multiple epiphyseal dysplasia HGNC:2227 Homo sapiens (human) 1311 COMP
  • MGI:6194238
DOID:4362 cervical cancer RGD:2886 Rattus norvegicus (Norway rat) 25325 Il10
  • MGI:6194238
DOID:0110229 cataract 6 multiple types MGI:95278 Mus musculus (house mouse) 13836 Epha2
  • MGI:6194238
  • PMID:19649315
DOID:557 kidney disease MGI:107164 Mus musculus (house mouse) 19055 Ppp3ca
  • MGI:6194238
DOID:2913 acute pancreatitis MGI:96677 Mus musculus (house mouse) 16590 Kit
  • MGI:6194238
DOID:0060669 cerebral cavernous malformation WB:WBGene00006897 Caenorhabditis elegans 186632 ver-4
  • MGI:6194238
DOID:7693 abdominal aortic aneurysm HGNC:8583 Homo sapiens (human) 5054 SERPINE1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:7739 Homo sapiens (human) 4747 NEFL
  • PMID:29368621
  • PMID:29391125
DOID:2841 asthma HGNC:6005 Homo sapiens (human) 59067 IL21
  • PMID:18802358
DOID:3620 central nervous system cancer MGI:97364 Mus musculus (house mouse) 18129 Notch2
  • MGI:6194238
DOID:10211 cholelithiasis HGNC:613 Homo sapiens (human) 348 APOE
  • PMID:18296645

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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