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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 6051 - 6075 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:4450 renal cell carcinoma MGI:104663 Mus musculus (house mouse) 16846 Lep
  • MGI:6194238
DOID:5016 hepatocellular clear cell carcinoma MGI:104663 Mus musculus (house mouse) 16846 Lep
  • MGI:6194238
DOID:11476 osteoporosis MGI:104663 Mus musculus (house mouse) 16846 Lep
  • MGI:6194238
DOID:11714 gestational diabetes MGI:104663 Mus musculus (house mouse) 16846 Lep
  • MGI:6194238
DOID:1338 congenital dyserythropoietic anemia MGI:104669 Mus musculus (house mouse) 17158 Man2a1
  • PMID:9230311
DOID:9074 systemic lupus erythematosus MGI:104669 Mus musculus (house mouse) 17158 Man2a1
  • PMID:11158608
DOID:13832 patent ductus arteriosus MGI:104672 Mus musculus (house mouse) 21419 Tfap2b
  • MGI:6194238
  • PMID:29804851
DOID:535 sleep disorder MGI:104672 Mus musculus (house mouse) 21419 Tfap2b
  • MGI:6194238
DOID:13550 angle-closure glaucoma MGI:104672 Mus musculus (house mouse) 21419 Tfap2b
  • PMID:27483349
DOID:0060563 Char syndrome MGI:104672 Mus musculus (house mouse) 21419 Tfap2b
  • MGI:6194238
  • PMID:21829553
DOID:14227 azoospermia MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • MGI:6194238
DOID:11198 DiGeorge syndrome MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • MGI:5284969
DOID:0060041 autism spectrum disorder MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • MGI:6194238
DOID:0081210 autosomal recessive intellectual developmental disorder 46 MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • MGI:6194238
DOID:3827 congenital diaphragmatic hernia MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • PMID:24355925
DOID:1059 intellectual disability MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • MGI:6194238
DOID:12716 newborn respiratory distress syndrome MGI:104719 Mus musculus (house mouse) 15531 Ndst1
  • PMID:10664446
  • PMID:10852901
DOID:9427 hypertensive encephalopathy MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • MGI:6194238
DOID:10908 hydrocephalus MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • MGI:6194238
DOID:10763 hypertension MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • MGI:6194238
DOID:1485 cystic fibrosis MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • MGI:6194238
DOID:9970 obesity MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • MGI:6194238
DOID:3393 coronary artery disease MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • MGI:6194238
DOID:10652 Alzheimer's disease MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • MGI:6194238
DOID:5419 schizophrenia MGI:104740 Mus musculus (house mouse) 19013 Ppara
  • PMID:33279456

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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