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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 401 - 425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0111237 congenital muscular dystrophy-dystroglycanopathy type A1 HGNC:9202 Homo sapiens (human) 10585 POMT1
  • MGI:6194238
  • RGD:7240710
DOID:2581 chondrodysplasia punctata HGNC:3133 Homo sapiens (human) 10682 EBP
  • PMID:10391218
DOID:0080352 X-linked chondrodysplasia punctata 2 HGNC:3133 Homo sapiens (human) 10682 EBP
  • RGD:7240710
DOID:0111865 MEND syndrome HGNC:3133 Homo sapiens (human) 10682 EBP
  • RGD:7240710
DOID:0060292 X-linked chondrodysplasia punctata 1 HGNC:3133 Homo sapiens (human) 10682 EBP
  • MGI:6194238
DOID:1508 candidiasis HGNC:4020 Homo sapiens (human) 10690 FUT9
  • MGI:6194238
DOID:0111451 progressive myoclonus epilepsy 8 HGNC:14253 Homo sapiens (human) 10715 CERS1
  • RGD:7240710
DOID:9352 type 2 diabetes mellitus HGNC:7056 Homo sapiens (human) 10724 OGA
  • MGI:6194238
DOID:1936 atherosclerosis HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:14736553
DOID:3181 oligodendroglioma HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:19347995
DOID:1612 breast cancer HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:20847343
DOID:576 proteinuria MGI:894701 Mus musculus (house mouse) 107895 Mgat5
  • MGI:6194238
DOID:0110312 hypertrophic cardiomyopathy 6 MGI:1336153 Mus musculus (house mouse) 108099 Prkag2
  • MGI:6194238
DOID:0090101 lethal congenital glycogen storage disease of heart MGI:1336153 Mus musculus (house mouse) 108099 Prkag2
  • MGI:6194238
DOID:384 Wolff-Parkinson-White syndrome MGI:1336153 Mus musculus (house mouse) 108099 Prkag2
  • MGI:6194238
DOID:2747 glycogen storage disease MGI:1336153 Mus musculus (house mouse) 108099 Prkag2
  • MGI:6194238
DOID:1289 neurodegenerative disease MGI:1336153 Mus musculus (house mouse) 108099 Prkag2
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II MGI:894694 Mus musculus (house mouse) 108148 Galnt2
  • MGI:6194238
DOID:9351 diabetes mellitus MGI:1339639 Mus musculus (house mouse) 108155 Ogt
  • MGI:6194238
DOID:0080240 non-syndromic X-linked intellectual disability 106 MGI:1339639 Mus musculus (house mouse) 108155 Ogt
  • MGI:6194238
DOID:6000 congestive heart failure MGI:1339639 Mus musculus (house mouse) 108155 Ogt
  • MGI:6194238
DOID:1712 aortic valve stenosis MGI:1339639 Mus musculus (house mouse) 108155 Ogt
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus MGI:1339639 Mus musculus (house mouse) 108155 Ogt
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2641 Homo sapiens (human) 10858 CYP46A1
  • PMID:12232784
DOID:2377 multiple sclerosis Xenbase:XB-GENE-17343520 Xenopus laevis (African clawed frog) 108695277 b4galt6.S
  • MGI:6194238

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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