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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 10151 - 10175 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence References
DOID:0050545 visceral heterotaxy HGNC:18053 Homo sapiens (human) 168507 PKD1L1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0080322 polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2 mutant phenotype evidence used in manual assertion
  • PMID:16943309
DOID:10941 intracranial aneurysm HGNC:9009 Homo sapiens (human) 5311 PKD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12842373
DOID:0110859 polycystic kidney disease 2 HGNC:9009 Homo sapiens (human) 5311 PKD2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:8466 retinal degeneration HGNC:9009 Homo sapiens (human) 5311 PKD2 mutant phenotype evidence used in manual assertion
  • PMID:16943309
DOID:898 autosomal dominant polycystic kidney disease HGNC:9009 Homo sapiens (human) 5311 PKD2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21115670
  • PMID:22863349
DOID:0080212 polycystic kidney disease 4 HGNC:9016 Homo sapiens (human) 5314 PKHD1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:9016 Homo sapiens (human) 5314 PKHD1 inference by association of genotype from phenotype used in manual assertion
  • PMID:11919560
  • PMID:12874454
DOID:0050565 autosomal recessive nonsyndromic deafness HGNC:20313 Homo sapiens (human) 93035 PKHD1L1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0111077 congenital nonspherocytic hemolytic anemia 2 HGNC:9020 Homo sapiens (human) 5313 PKLR inference by association of genotype from phenotype used in manual assertion
  • PMID:16704447
  • RGD:7240710
DOID:12365 malaria HGNC:9020 Homo sapiens (human) 5313 PKLR inference by association of genotype from phenotype used in manual assertion
  • PMID:20377593
DOID:0111077 congenital nonspherocytic hemolytic anemia 2 HGNC:9020 Homo sapiens (human) 5313 PKLR mutant phenotype evidence used in manual assertion
  • PMID:19755962
DOID:9352 type 2 diabetes mellitus HGNC:9020 Homo sapiens (human) 5313 PKLR inference by association of genotype from phenotype used in manual assertion
  • PMID:12196482
DOID:1926 Gaucher's disease HGNC:9020 Homo sapiens (human) 5313 PKLR inference by association of genotype from phenotype used in manual assertion
  • PMID:9677056
DOID:2861 congenital nonspherocytic hemolytic anemia HGNC:9020 Homo sapiens (human) 5313 PKLR inference by association of genotype from phenotype used in manual assertion
  • PMID:11054094
  • PMID:1536957
  • PMID:7949104
  • PMID:8161798
DOID:0110077 arrhythmogenic right ventricular dysplasia 9 HGNC:9024 Homo sapiens (human) 5318 PKP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:9024 Homo sapiens (human) 5318 PKP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15489853
  • PMID:16567567
DOID:9256 colorectal cancer HGNC:9031 Homo sapiens (human) 5320 PLA2G2A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:11151 cholecystolithiasis HGNC:9031 Homo sapiens (human) 5320 PLA2G2A direct assay evidence used in manual assertion
  • PMID:9695991
DOID:8534 gastroesophageal reflux disease HGNC:9031 Homo sapiens (human) 5320 PLA2G2A mutant phenotype evidence used in manual assertion
  • PMID:19672667
DOID:526 human immunodeficiency virus infectious disease HGNC:9031 Homo sapiens (human) 5320 PLA2G2A inference by association of genotype from phenotype used in manual assertion
  • PMID:18096355
DOID:0111677 familial benign fleck retina HGNC:9038 Homo sapiens (human) 5322 PLA2G5 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:20938027
DOID:0110735 neurodegeneration with brain iron accumulation 2a HGNC:9039 Homo sapiens (human) 8398 PLA2G6 inference by association of genotype from phenotype used in manual assertion
  • PMID:22934738
  • RGD:7240710
DOID:0110736 neurodegeneration with brain iron accumulation 2b HGNC:9039 Homo sapiens (human) 8398 PLA2G6 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: April 7, 2025