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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 13376 - 13400 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB ▲ Evidence References
DOID:684 hepatocellular carcinoma HGNC:20456 Homo sapiens (human) 84231 TRAF7 mutant phenotype evidence used in manual assertion
  • PMID:31730901
DOID:0080236 autosomal dominant intellectual developmental disorder 45 HGNC:14214 Homo sapiens (human) 23152 CIC inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:3908 lung non-small cell carcinoma HGNC:24308 Homo sapiens (human) 81037 CLPTM1L inference by association of genotype from phenotype used in manual assertion
  • PMID:24679952
DOID:4448 macular degeneration HGNC:3467 Homo sapiens (human) 2099 ESR1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17325140
DOID:224 transient cerebral ischemia RGD:620598 Rattus norvegicus (Norway rat) 114243 Nox1 mutant phenotype evidence used in manual assertion
  • PMID:25617620
DOID:2841 asthma HGNC:1331 Homo sapiens (human) 727 C5 inference by association of genotype from phenotype used in manual assertion
  • PMID:15278436
DOID:10908 hydrocephalus RGD:619777 Rattus norvegicus (Norway rat) 50687 L1cam mutant phenotype evidence used in manual assertion
  • PMID:30738385
DOID:4483 rhinitis HGNC:6015 Homo sapiens (human) 3566 IL4R inference by association of genotype from phenotype used in manual assertion
  • PMID:15564773
DOID:6000 congestive heart failure RGD:1565646 Rattus norvegicus (Norway rat) 499593 Sox2 mutant phenotype evidence used in manual assertion
  • PMID:34321385
DOID:1852 intrahepatic cholestasis HGNC:42 Homo sapiens (human) 8647 ABCB11 inference by association of genotype from phenotype used in manual assertion
  • PMID:9806540
DOID:13482 Proteus syndrome MGI:87986 Mus musculus (house mouse) 11651 Akt1 author statement supported by traceable reference
  • PMID:31194862
DOID:10652 Alzheimer's disease HGNC:7154 Homo sapiens (human) 4311 MME inference by association of genotype from phenotype used in manual assertion
  • PMID:15860464
  • PMID:17928142
  • PMID:22493749
  • PMID:28294061
DOID:0060256 Dowling-Degos disease HGNC:22954 Homo sapiens (human) 56983 POGLUT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111095 Fanconi anemia complementation group A MGI:1341823 Mus musculus (house mouse) 14087 Fanca author statement supported by traceable reference
  • PMID:10915769
  • PMID:12913077
DOID:14731 Weaver syndrome HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease WB:WBGene00002048 Caenorhabditis elegans 175807 ida-1 mutant phenotype evidence used in manual assertion
  • PMID:25469508
DOID:9352 type 2 diabetes mellitus HGNC:381 Homo sapiens (human) 231 AKR1B1 inference by association of genotype from phenotype used in manual assertion
  • PMID:15569136
DOID:13359 Ehlers-Danlos syndrome HGNC:218 Homo sapiens (human) 9509 ADAMTS2 inference by association of genotype from phenotype used in manual assertion
  • PMID:10417273
DOID:0081450 hyperimmunoglobulinemia D periodic fever syndrome HGNC:7530 Homo sapiens (human) 4598 MVK inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:1788 peritoneal mesothelioma HGNC:20456 Homo sapiens (human) 84231 TRAF7 inference by association of genotype from phenotype used in manual assertion
  • PMID:30171198
DOID:6688 autoimmune lymphoproliferative syndrome MGI:99255 Mus musculus (house mouse) 14103 Fasl author statement supported by traceable reference
  • MGI:77345
  • PMID:6693832
DOID:0111027 hemochromatosis type 2A MGI:1916835 Mus musculus (house mouse) 69585 Hjv author statement supported by traceable reference
  • PMID:16075058
  • PMID:16075059
DOID:8946 severe nonproliferative diabetic retinopathy MGI:97531 Mus musculus (house mouse) 18596 Pdgfrb author statement supported by traceable reference
  • PMID:23633653
DOID:9169 Wiskott-Aldrich syndrome SGD:S000005707 Saccharomyces cerevisiae S288C 854353 LAS17 genetic interaction evidence used in manual assertion
  • PMID:16488394
  • PMID:19817875
DOID:1324 lung cancer HGNC:30635 Homo sapiens (human) 11063 SOX30 mutant phenotype evidence used in manual assertion
  • PMID:25435374
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025