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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 3001 - 3025 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10652 Alzheimer's disease HGNC:3350 Homo sapiens (human) 2023 ENO1
  • PMID:17387692
DOID:10763 hypertension HGNC:3350 Homo sapiens (human) 2023 ENO1
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:14115 toxic shock syndrome HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:11054 urinary bladder cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:17951193
DOID:10763 hypertension HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21130083
DOID:3459 breast carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:16608642
DOID:1800 neuroendocrine carcinoma HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15010880
DOID:11832 visual epilepsy HGNC:3353 Homo sapiens (human) 2026 ENO2
  • MGI:6194238
DOID:936 brain disease HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:20847541
DOID:12783 migraine without aura HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:21293918
DOID:10283 prostate cancer HGNC:3353 Homo sapiens (human) 2026 ENO2
  • PMID:15239127
DOID:1712 aortic valve stenosis HGNC:3354 Homo sapiens (human) 2027 ENO3
  • MGI:6194238
DOID:0081376 obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy MGI:98266 Mus musculus (house mouse) 20322 Sord
  • MGI:6194238
DOID:0081427 autosomal recessive distal hereditary motor neuronopathy 8 MGI:98266 Mus musculus (house mouse) 20322 Sord
  • MGI:6194238
DOID:83 cataract MGI:98266 Mus musculus (house mouse) 20322 Sord
  • PMID:18760274
DOID:9743 diabetic neuropathy MGI:98266 Mus musculus (house mouse) 20322 Sord
  • MGI:6194238
DOID:0060718 autosomal recessive congenital ichthyosis 9 HGNC:23752 Homo sapiens (human) 204219 CERS3
  • RGD:7240710
DOID:3070 high grade glioma MGI:108470 Mus musculus (house mouse) 20440 St6gal1
  • MGI:6194238
DOID:1574 alcohol use disorder MGI:108470 Mus musculus (house mouse) 20440 St6gal1
  • MGI:6194238
DOID:0080414 developmental and epileptic encephalopathy 15 MGI:1316659 Mus musculus (house mouse) 20441 St3gal3
  • MGI:6194238
DOID:0081180 autosomal recessive intellectual developmental disorder 12 MGI:1316659 Mus musculus (house mouse) 20441 St3gal3
  • MGI:6194238
DOID:0050589 inflammatory bowel disease MGI:1341826 Mus musculus (house mouse) 20445 St6galnac1
  • PMID:35303419
DOID:0060470 salt and pepper syndrome MGI:1339963 Mus musculus (house mouse) 20454 St3gal5
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:3402 Homo sapiens (human) 2053 EPHX2
  • PMID:14732757

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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