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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 January 28, 2025
Displaying entries 10051 - 10075 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:13515 tuberous sclerosis HGNC:12362 Homo sapiens (human) 7248 TSC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:16114042
  • PMID:25900779
  • PMID:9242607
DOID:5517 stomach carcinoma HGNC:3689 Homo sapiens (human) 2263 FGFR2 mutant phenotype evidence used in manual assertion
  • PMID:31255687
DOID:9256 colorectal cancer HGNC:9801 Homo sapiens (human) 5879 RAC1 mutant phenotype evidence used in manual assertion
  • PMID:29884911
DOID:0080074 neural tube defect HGNC:1550 Homo sapiens (human) 875 CBS inference by association of genotype from phenotype used in manual assertion
  • PMID:12649066
DOID:11247 disseminated intravascular coagulation HGNC:3541 Homo sapiens (human) 2152 F3 direct assay evidence used in manual assertion
  • PMID:3802033
DOID:874 bacterial pneumonia HGNC:11892 Homo sapiens (human) 7124 TNF direct assay evidence used in manual assertion
  • PMID:7546648
DOID:5082 liver cirrhosis HGNC:3025 Homo sapiens (human) 1815 DRD4 inference by association of genotype from phenotype used in manual assertion
  • PMID:23298155
DOID:0110083 arrhythmogenic right ventricular dysplasia 12 HGNC:6207 Homo sapiens (human) 3728 JUP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4947 cholangiocarcinoma HGNC:11936 Homo sapiens (human) 356 FASLG direct assay evidence used in manual assertion
  • PMID:11029528
DOID:3145 hyperlipoproteinemia type III HGNC:613 Homo sapiens (human) 348 APOE inference by association of genotype from phenotype used in manual assertion
  • PMID:199847
  • PMID:7175379
  • RGD:7240710
DOID:0110195 Charcot-Marie-Tooth disease type 4E HGNC:3239 Homo sapiens (human) 1959 EGR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:2841 asthma HGNC:2438 Homo sapiens (human) 1440 CSF3 direct assay evidence used in manual assertion
  • PMID:21396376
DOID:2349 arteriosclerosis HGNC:3467 Homo sapiens (human) 2099 ESR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17903303
DOID:684 hepatocellular carcinoma MGI:99421 Mus musculus (house mouse) 18023 Nfe2l1 author statement supported by traceable reference
  • PMID:15738389
DOID:0050742 nicotine dependence HGNC:12008 Homo sapiens (human) 7166 TPH1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15635702
DOID:2746 glycogen storage disease V HGNC:9726 Homo sapiens (human) 5837 PYGM inference by association of genotype from phenotype used in manual assertion
  • PMID:9633816
  • RGD:7240710
DOID:10763 hypertension HGNC:1929 Homo sapiens (human) 1113 CHGA inference by association of genotype from phenotype used in manual assertion
  • PMID:21061160
DOID:684 hepatocellular carcinoma MGI:1919815 Mus musculus (house mouse) 72565 Uaca author statement supported by traceable reference
  • PMID:19637241
DOID:384 Wolff-Parkinson-White syndrome MGI:1338938 Mus musculus (house mouse) 12166 Bmpr1a author statement supported by traceable reference
  • PMID:16037571
DOID:9744 type 1 diabetes mellitus HGNC:5472 Homo sapiens (human) 3486 IGFBP3 direct assay evidence used in manual assertion
  • PMID:15356074
DOID:0050700 cardiomyopathy MGI:96828 Mus musculus (house mouse) 16971 Lrp1 author statement supported by traceable reference
  • PMID:24312398
DOID:3490 Noonan syndrome HGNC:9644 Homo sapiens (human) 5781 PTPN11 inference by association of genotype from phenotype used in manual assertion
  • PMID:11992261
DOID:0060887 ossification of the posterior longitudinal ligament of spine HGNC:3356 Homo sapiens (human) 5167 ENPP1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15834329
DOID:9970 obesity HGNC:8156 Homo sapiens (human) 4988 OPRM1 direct assay evidence used in manual assertion
  • PMID:31258545
DOID:0110953 Waardenburg syndrome type 4A HGNC:3180 Homo sapiens (human) 1910 EDNRB inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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Supported by JST NBDC Grant Number JPMJND2204

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