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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 201 - 225 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050534 congenital stationary night blindness HGNC:4689 Homo sapiens (human) 3000 GUCY2D inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050534 congenital stationary night blindness HGNC:7146 Homo sapiens (human) 4308 TRPM1 inference by association of genotype from phenotype used in manual assertion
  • PMID:19878917
  • PMID:19896109
  • PMID:19896113
DOID:0050534 congenital stationary night blindness HGNC:1393 Homo sapiens (human) 778 CACNA1F inference by association of genotype from phenotype used in manual assertion
  • PMID:12111638
DOID:0050535 exudative vitreoretinopathy MGI:108520 Mus musculus (house mouse) 14366 Fzd4 author statement supported by traceable reference
  • PMID:20159112
  • PMID:33497368
DOID:0050535 exudative vitreoretinopathy MGI:105057 Mus musculus (house mouse) 12562 Cdh5 author statement supported by traceable reference
  • PMID:33497368
DOID:0050535 exudative vitreoretinopathy MGI:1278315 Mus musculus (house mouse) 16973 Lrp5 author statement supported by traceable reference
  • PMID:18263894
  • PMID:27524797
  • PMID:33497368
DOID:0050535 exudative vitreoretinopathy MGI:88276 Mus musculus (house mouse) 12387 Ctnnb1 author statement supported by traceable reference
  • PMID:33497368
DOID:0050540 Charcot-Marie-Tooth disease type 3 HGNC:7225 Homo sapiens (human) 4359 MPZ inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050540 Charcot-Marie-Tooth disease type 3 MGI:97631 Mus musculus (house mouse) 18858 Pmp22 author statement supported by traceable reference
  • MGI:5515889
DOID:0050540 Charcot-Marie-Tooth disease type 3 MGI:103177 Mus musculus (house mouse) 17528 Mpz author statement supported by traceable reference
  • PMID:16495463
  • PMID:7581451
DOID:0050540 Charcot-Marie-Tooth disease type 3 HGNC:9118 Homo sapiens (human) 5376 PMP22 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050540 Charcot-Marie-Tooth disease type 3 HGNC:3239 Homo sapiens (human) 1959 EGR2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050545 visceral heterotaxy MGI:2664387 Mus musculus (house mouse) 214766 Mmp21 author statement supported by traceable reference
  • MGI:5284969
DOID:0050545 visceral heterotaxy MGI:1100864 Mus musculus (house mouse) 13411 Dnah11 author statement supported by traceable reference
  • MGI:5284969
DOID:0050545 visceral heterotaxy MGI:97515 Mus musculus (house mouse) 18552 Pcsk5 author statement supported by traceable reference
  • MGI:5284969
DOID:0050545 visceral heterotaxy MGI:87912 Mus musculus (house mouse) 11481 Acvr2b author statement supported by traceable reference
  • PMID:9242489
DOID:0050545 visceral heterotaxy MGI:109448 Mus musculus (house mouse) 12627 Cfc1 author statement supported by traceable reference
  • MGI:5284969
DOID:0050545 visceral heterotaxy HGNC:33983 Homo sapiens (human) 653275 CFC1B inference by association of genotype from phenotype used in manual assertion
  • PMID:11062482
  • PMID:25423076
DOID:0050545 visceral heterotaxy HGNC:4214 Homo sapiens (human) 2657 GDF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:174 Homo sapiens (human) 93 ACVR2B inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050545 visceral heterotaxy HGNC:7865 Homo sapiens (human) 4838 NODAL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050545 visceral heterotaxy MGI:107718 Mus musculus (house mouse) 110082 Dnah5 author statement supported by traceable reference
  • MGI:5284969
DOID:0050545 visceral heterotaxy MGI:1916172 Mus musculus (house mouse) 68922 Dnai1 author statement supported by traceable reference
  • MGI:5284969
DOID:0050545 visceral heterotaxy MGI:1923928 Mus musculus (house mouse) 329795 Tmem67 author statement supported by traceable reference
  • MGI:5284969
DOID:0050545 visceral heterotaxy HGNC:18053 Homo sapiens (human) 168507 PKD1L1 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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Last updated: August 4, 2025