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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 13051 - 13075 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:784 chronic kidney disease RGD:2072 Rattus norvegicus (Norway rat) 24182 Agtr2 mutant phenotype evidence used in manual assertion
  • PMID:12089373
DOID:2841 asthma HGNC:11527 Homo sapiens (human) 6865 TACR2 mutant phenotype evidence used in manual assertion
  • PMID:19880429
DOID:1793 pancreatic cancer HGNC:5975 Homo sapiens (human) 3598 IL13RA2 mutant phenotype evidence used in manual assertion
  • PMID:11748276
DOID:10652 Alzheimer's disease RGD:620349 Rattus norvegicus (Norway rat) 29527 Ptgs2 mutant phenotype evidence used in manual assertion
  • PMID:21701788
DOID:0111862 congenital bilateral absence of vas deferens RGD:2332 Rattus norvegicus (Norway rat) 24255 Cftr mutant phenotype evidence used in manual assertion
  • PMID:24608905
DOID:5844 myocardial infarction RGD:3233 Rattus norvegicus (Norway rat) 24613 Oprd1 mutant phenotype evidence used in manual assertion
  • PMID:15076225
DOID:670 amphetamine abuse RGD:3729 Rattus norvegicus (Norway rat) 29219 Snca mutant phenotype evidence used in manual assertion
  • PMID:20551914
DOID:1059 intellectual disability WB:WBGene00003182 Caenorhabditis elegans 172732 mef-2 mutant phenotype evidence used in manual assertion
  • PMID:22859820
DOID:2921 glomerulonephritis RGD:2311 Rattus norvegicus (Norway rat) 25407 Cd59b mutant phenotype evidence used in manual assertion
  • PMID:7523753
DOID:3459 breast carcinoma HGNC:2705 Homo sapiens (human) 1634 DCN mutant phenotype evidence used in manual assertion
  • PMID:18688028
DOID:2256 osteochondrodysplasia HGNC:2200 Homo sapiens (human) 1280 COL2A1 mutant phenotype evidence used in manual assertion
  • PMID:15476249
DOID:11723 Duchenne muscular dystrophy HGNC:6143 Homo sapiens (human) 3679 ITGA7 mutant phenotype evidence used in manual assertion
  • PMID:23319059
DOID:14330 Parkinson's disease RGD:620598 Rattus norvegicus (Norway rat) 114243 Nox1 mutant phenotype evidence used in manual assertion
  • PMID:23077033
DOID:9743 diabetic neuropathy RGD:2202 Rattus norvegicus (Norway rat) 24225 Bdnf mutant phenotype evidence used in manual assertion
  • PMID:20557422
DOID:10652 Alzheimer's disease HGNC:7782 Homo sapiens (human) 4780 NFE2L2 mutant phenotype evidence used in manual assertion
  • PMID:19805328
DOID:2723 dermatitis HGNC:5960 Homo sapiens (human) 3551 IKBKB mutant phenotype evidence used in manual assertion
  • PMID:20200541
DOID:0070355 overactive bladder syndrome RGD:1303284 Rattus norvegicus (Norway rat) 312896 Trpa1 mutant phenotype evidence used in manual assertion
  • PMID:21367919
DOID:3803 Crigler-Najjar syndrome HGNC:12530 Homo sapiens (human) 54658 UGT1A1 mutant phenotype evidence used in manual assertion
  • PMID:16019265
  • PMID:16337205
  • PMID:22094718
  • PMID:24285217
DOID:0080301 atypical hemolytic-uremic syndrome HGNC:4883 Homo sapiens (human) 3075 CFH mutant phenotype evidence used in manual assertion
  • PMID:17517971
DOID:5223 infertility RGD:2581 Rattus norvegicus (Norway rat) 24890 Esr1 mutant phenotype evidence used in manual assertion
  • PMID:24506075
DOID:615 leukopenia HGNC:2561 Homo sapiens (human) 7852 CXCR4 mutant phenotype evidence used in manual assertion
  • PMID:21890643
DOID:552 pneumonia HGNC:10803 Homo sapiens (human) 6441 SFTPD mutant phenotype evidence used in manual assertion
  • PMID:17925426
DOID:219 colon cancer HGNC:1455 Homo sapiens (human) 811 CALR mutant phenotype evidence used in manual assertion
  • PMID:19256344
DOID:557 kidney disease WB:WBGene00016848 Caenorhabditis elegans 177557 klo-1 mutant phenotype evidence used in manual assertion
  • PMID:21177529
DOID:11394 adult respiratory distress syndrome RGD:70553 Rattus norvegicus (Norway rat) 113959 C5ar1 mutant phenotype evidence used in manual assertion
  • PMID:16782534
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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: December 8, 2025