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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 101 - 125 of 14279 in total
Disease ID ▲ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:6636 Homo sapiens (human) 4000 LMNA inference by association of genotype from phenotype used in manual assertion
  • PMID:25837155
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:3036 Homo sapiens (human) 1824 DSC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:25497880
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:11769 Homo sapiens (human) 7043 TGFB3 inference by association of genotype from phenotype used in manual assertion
  • PMID:7951245
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:3049 Homo sapiens (human) 1829 DSG2 mutant phenotype evidence used in manual assertion
  • PMID:30304392
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:3049 Homo sapiens (human) 1829 DSG2 inference by association of genotype from phenotype used in manual assertion
  • PMID:30454721
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy ZFIN:ZDB-GENE-031116-55 Danio rerio (zebrafish) 560091 dsc2l author statement supported by traceable reference used in manual assertion
  • PMID:33784018
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:2770 Homo sapiens (human) 1674 DES inference by association of genotype from phenotype used in manual assertion
  • PMID:29212896
DOID:0050431 arrhythmogenic right ventricular cardiomyopathy HGNC:28472 Homo sapiens (human) 79188 TMEM43 inference by association of genotype from phenotype used in manual assertion
  • PMID:10631146
DOID:0050432 Asperger syndrome HGNC:10982 Homo sapiens (human) 8604 SLC25A12 inference by association of genotype from phenotype used in manual assertion
  • PMID:24679184
DOID:0050433 fatal familial insomnia MGI:97769 Mus musculus (house mouse) 19122 Prnp author statement supported by traceable reference
  • PMID:19709627
  • PMID:23959875
DOID:0050433 fatal familial insomnia HGNC:9449 Homo sapiens (human) 5621 PRNP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050436 mulibrey nanism HGNC:7523 Homo sapiens (human) 4591 TRIM37 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050436 mulibrey nanism MGI:2153072 Mus musculus (house mouse) 68729 Trim37 author statement supported by traceable reference
  • PMID:27044324
DOID:0050437 Danon disease HGNC:6501 Homo sapiens (human) 3920 LAMP2 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050437 Danon disease RGD:2990 Rattus norvegicus (Norway rat) 24944 Lamp2 mutant phenotype evidence used in manual assertion
  • PMID:29720683
DOID:0050437 Danon disease MGI:96748 Mus musculus (house mouse) 16784 Lamp2 author statement supported by traceable reference
  • PMID:10972293
  • PMID:28526246
  • PMID:34459252
DOID:0050439 Usher syndrome HGNC:7606 Homo sapiens (human) 4647 MYO7A direct assay evidence used in manual assertion
  • PMID:23991031
DOID:0050439 Usher syndrome HGNC:12601 Homo sapiens (human) 7399 USH2A inference by association of genotype from phenotype used in manual assertion
  • PMID:18452394
DOID:0050439 Usher syndrome HGNC:7606 Homo sapiens (human) 4647 MYO7A inference by association of genotype from phenotype used in manual assertion
  • PMID:12112664
  • PMID:8900236
  • RGD:7240710
DOID:0050439 Usher syndrome HGNC:24102 Homo sapiens (human) 22901 ARSG inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050440 familial partial lipodystrophy HGNC:6636 Homo sapiens (human) 4000 LMNA inference by association of genotype from phenotype used in manual assertion
  • PMID:10655060
DOID:0050440 familial partial lipodystrophy HGNC:281 Homo sapiens (human) 150 ADRA2A inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050440 familial partial lipodystrophy MGI:97747 Mus musculus (house mouse) 19016 Pparg author statement supported by traceable reference
  • PMID:17921248
DOID:0050441 mucosulfatidosis HGNC:20376 Homo sapiens (human) 285362 SUMF1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050441 mucosulfatidosis MGI:1889844 Mus musculus (house mouse) 58911 Sumf1 author statement supported by traceable reference
  • PMID:17360554
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