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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 951 - 975 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▲ References
DOID:2741 bilirubin metabolic disorder RGD:3935 Rattus norvegicus (Norway rat) 24861 Ugt1a1
  • MGI:6194238
  • PMID:15753292
DOID:4947 cholangiocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
  • PMID:12692057
DOID:0110853 rhizomelic chondrodysplasia punctata type 3 HGNC:327 Homo sapiens (human) 8540 AGPS
  • MGI:6194238
  • RGD:7240710
DOID:0050560 Walker-Warburg syndrome HGNC:19743 Homo sapiens (human) 29954 POMT2
  • MGI:6194238
  • PMID:15894594
DOID:0110958 Gaucher's disease type II HGNC:4177 Homo sapiens (human) 2629 GBA1
  • MGI:6194238
  • RGD:7240710
DOID:0111027 hemochromatosis type 2A HGNC:4887 Homo sapiens (human) 148738 HJV
  • MGI:6194238
  • RGD:7240710
DOID:0060849 osteoporosis-pseudoglioma syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • MGI:6194238
  • PMID:11719191
  • PMID:16679074
  • RGD:7240710
DOID:10587 Krabbe disease HGNC:4115 Homo sapiens (human) 2581 GALC
  • MGI:6194238
  • RGD:7240710
DOID:4928 intrahepatic cholangiocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
  • PMID:24139215
DOID:684 hepatocellular carcinoma HGNC:9232 Homo sapiens (human) 5465 PPARA
  • MGI:6194238
  • PMID:19119483
DOID:9775 diastolic heart failure HGNC:2707 Homo sapiens (human) 1636 ACE
  • MGI:6194238
  • PMID:19021695
  • PMID:19752885
DOID:10652 Alzheimer's disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
  • PMID:19154537
  • PMID:24101602
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:13628 favism HGNC:4057 Homo sapiens (human) 2539 G6PD
  • MGI:6194238
  • RGD:7240710
DOID:0080124 mitochondrial DNA depletion syndrome 5 HGNC:11448 Homo sapiens (human) 8803 SUCLA2
  • MGI:6194238
  • RGD:7240710
DOID:0111619 combined D-2- and L-2-hydroxyglutaric aciduria HGNC:10979 Homo sapiens (human) 6576 SLC25A1
  • MGI:6194238
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:16750516
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q HGNC:23537 Homo sapiens (human) 55526 DHTKD1
  • MGI:6194238
  • RGD:7240710
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:18590 Homo sapiens (human) 80339 PNPLA3
  • MGI:6194238
  • PMID:24477042
  • PMID:24831885
  • PMID:26740948
DOID:0070238 primary coenzyme Q10 deficiency 1 HGNC:25223 Homo sapiens (human) 27235 COQ2
  • MGI:6194238
  • RGD:7240710
DOID:10763 hypertension HGNC:12518 Homo sapiens (human) 7351 UCP2
  • MGI:6194238
  • PMID:15106800
DOID:206 hereditary multiple exostoses HGNC:3512 Homo sapiens (human) 2131 EXT1
  • MGI:6194238
  • PMID:12490068
  • PMID:17767039
  • PMID:18330718
  • PMID:24297320
  • PMID:25421355
  • PMID:26839764
  • PMID:8981950
DOID:1612 breast cancer HGNC:8975 Homo sapiens (human) 5290 PIK3CA
  • MGI:6194238
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:5993 Homo sapiens (human) 3554 IL1R1
  • MGI:6194238
  • PMID:11197691
  • PMID:8911996
DOID:3070 high grade glioma HGNC:5382 Homo sapiens (human) 3417 IDH1
  • MGI:6194238
  • RGD:7240710

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Last updated: August 19, 2024