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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:0050905 inflammatory myofibroblastic tumor HGNC:9848 Homo sapiens (human) 5903 RANBP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:12661011
DOID:1024 leprosy HGNC:10907 Homo sapiens (human) 6556 SLC11A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10608779
  • PMID:15755200
DOID:0110861 autosomal recessive polycystic kidney disease RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:20229187
DOID:437 myasthenia gravis HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10593018
  • PMID:19561379
DOID:1793 pancreatic cancer HGNC:1511 Homo sapiens (human) 842 CASP9 inference by association of genotype from phenotype used in manual assertion
  • PMID:20357690
DOID:8466 retinal degeneration FB:FBgn0031414 Drosophila melanogaster (fruit fly) 3771890 eys combinatorial experimental and author inference evidence used in manual assertion
  • PMID:24705015
DOID:8398 osteoarthritis HGNC:7673 Homo sapiens (human) 9612 NCOR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15334463
DOID:9452 steatotic liver disease MGI:96765 Mus musculus (house mouse) 16835 Ldlr author statement supported by traceable reference
  • PMID:21690266
DOID:980 choroidal sclerosis HGNC:4689 Homo sapiens (human) 3000 GUCY2D inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:12930 dilated cardiomyopathy HGNC:17997 Homo sapiens (human) 79147 FKRP inference by association of genotype from phenotype used in manual assertion
  • PMID:15833432
DOID:0112374 muscular dystrophy-dystroglycanopathy HGNC:22932 Homo sapiens (human) 29925 GMPPB inference by association of genotype from phenotype used in manual assertion
  • PMID:26310427
DOID:0060201 amyotrophic lateral sclerosis type 10 HGNC:11571 Homo sapiens (human) 23435 TARDBP inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110131 Bardet-Biedl syndrome 9 HGNC:30000 Homo sapiens (human) 27241 BBS9 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:9256 colorectal cancer HGNC:2602 Homo sapiens (human) 1591 CYP24A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:24562971
  • PMID:28821819
  • PMID:31802707
  • PMID:33504116
DOID:12849 autistic disorder HGNC:13875 Homo sapiens (human) 93986 FOXP2 inference by association of genotype from phenotype used in manual assertion
  • PMID:15108192
  • PMID:15737702
DOID:2569 retinal drusen HGNC:4883 Homo sapiens (human) 3075 CFH inference by association of genotype from phenotype used in manual assertion
  • PMID:18936151
  • PMID:22491393
DOID:1205 allergic disease HGNC:4948 Homo sapiens (human) 3123 HLA-DRB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:10689122
  • PMID:15853900
  • PMID:16112029
DOID:1612 breast cancer HGNC:2529 Homo sapiens (human) 1509 CTSD mutant phenotype evidence used in manual assertion
  • PMID:12140763
DOID:0060170 generalized epilepsy with febrile seizures plus MGI:98247 Mus musculus (house mouse) 20266 Scn1b author statement supported by traceable reference
  • PMID:20628201
DOID:397 restrictive cardiomyopathy MGI:98783 Mus musculus (house mouse) 21954 Tnni3 author statement supported by traceable reference
  • PMID:17027633
  • PMID:22683325
DOID:9252 amino acid metabolic disorder HGNC:8923 Homo sapiens (human) 26227 PHGDH inference by association of genotype from phenotype used in manual assertion
  • PMID:11055895
DOID:10534 stomach cancer HGNC:6018 Homo sapiens (human) 3569 IL6 inference by association of genotype from phenotype used in manual assertion
  • PMID:27049718
  • PMID:28442395
DOID:0080855 Parkinsonism HGNC:16369 Homo sapiens (human) 11315 PARK7 mutant phenotype evidence used in manual assertion
  • PMID:16860563
DOID:1214 tympanosclerosis HGNC:11850 Homo sapiens (human) 7099 TLR4 inference by association of genotype from phenotype used in manual assertion
  • PMID:19398177
DOID:13963 nuclear senile cataract HGNC:24678 Homo sapiens (human) 79068 FTO inference by association of genotype from phenotype used in manual assertion
  • PMID:19329528
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Supported by JST NBDC Grant Number JPMJND2204

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