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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 13151 - 13175 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence ▲ References
DOID:8584 Burkitt lymphoma HGNC:11919 Homo sapiens (human) 958 CD40 mutant phenotype evidence used in manual assertion
  • PMID:9192773
DOID:0110299 autosomal recessive limb-girdle muscular dystrophy type 2I HGNC:17997 Homo sapiens (human) 79147 FKRP mutant phenotype evidence used in manual assertion
  • PMID:25048216
DOID:2476 hereditary spastic paraplegia SGD:S000005691 Saccharomyces cerevisiae S288C 854336 SEY1 mutant phenotype evidence used in manual assertion
  • PMID:19665976
DOID:8283 peritonitis HGNC:3823 Homo sapiens (human) 27086 FOXP1 mutant phenotype evidence used in manual assertion
  • PMID:18799727
DOID:10230 aortic atherosclerosis RGD:2998 Rattus norvegicus (Norway rat) 300438 Ldlr mutant phenotype evidence used in manual assertion
  • PMID:29459263
DOID:0111446 progressive myoclonus epilepsy 3 SGD:S000005569 Saccharomyces cerevisiae S288C 854208 WHI2 mutant phenotype evidence used in manual assertion
  • PMID:30295347
DOID:14330 Parkinson's disease HGNC:4851 Homo sapiens (human) 3064 HTT mutant phenotype evidence used in manual assertion
  • PMID:26192120
DOID:397 restrictive cardiomyopathy HGNC:6846 Homo sapiens (human) 5608 MAP2K6 mutant phenotype evidence used in manual assertion
  • PMID:11593045
DOID:9976 heroin dependence RGD:68946 Rattus norvegicus (Norway rat) 29237 Penk mutant phenotype evidence used in manual assertion
  • PMID:22683090
DOID:783 end stage renal disease RGD:2493 Rattus norvegicus (Norway rat) 24310 Ace mutant phenotype evidence used in manual assertion
  • PMID:14586729
DOID:12134 factor VIII deficiency HGNC:11760 Homo sapiens (human) 7035 TFPI mutant phenotype evidence used in manual assertion
  • PMID:24263002
DOID:1561 cognitive disorder HGNC:620 Homo sapiens (human) 351 APP mutant phenotype evidence used in manual assertion
  • PMID:19101630
DOID:1168 familial hyperlipidemia RGD:3560 Rattus norvegicus (Norway rat) 25106 Rgn mutant phenotype evidence used in manual assertion
  • PMID:15375596
DOID:1074 kidney failure RGD:3825 Rattus norvegicus (Norway rat) 24816 Tbxa2r mutant phenotype evidence used in manual assertion
  • PMID:9893136
DOID:10247 pleurisy RGD:61897 Rattus norvegicus (Norway rat) 58949 Ptafr mutant phenotype evidence used in manual assertion
  • PMID:8395390
DOID:3347 osteosarcoma HGNC:2730 Homo sapiens (human) 780 DDR1 mutant phenotype evidence used in manual assertion
  • PMID:29039472
DOID:0080556 congenital disorder of glycosylation Id SGD:S000000178 Saccharomyces cerevisiae S288C 852196 ALG3 mutant phenotype evidence used in manual assertion
  • PMID:23038983
DOID:10286 prostate carcinoma HGNC:11364 Homo sapiens (human) 6774 STAT3 mutant phenotype evidence used in manual assertion
  • PMID:18210874
DOID:684 hepatocellular carcinoma HGNC:11063 Homo sapiens (human) 8140 SLC7A5 mutant phenotype evidence used in manual assertion
  • PMID:26389641
DOID:552 pneumonia RGD:3644 Rattus norvegicus (Norway rat) 29397 Ccl11 mutant phenotype evidence used in manual assertion
  • PMID:10595930
DOID:1793 pancreatic cancer HGNC:5973 Homo sapiens (human) 3596 IL13 mutant phenotype evidence used in manual assertion
  • PMID:12808442
DOID:0080195 Marinesco-Sjogren syndrome SGD:S000005391 Saccharomyces cerevisiae S288C 854126 SIL1 mutant phenotype evidence used in manual assertion
  • PMID:28257000
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:16940 Homo sapiens (human) 84649 DGAT2 mutant phenotype evidence used in manual assertion
  • PMID:17618857
DOID:3021 acute kidney failure HGNC:11784 Homo sapiens (human) 7056 THBD mutant phenotype evidence used in manual assertion
  • PMID:17804460
DOID:13139 crescentic glomerulonephritis RGD:620195 Rattus norvegicus (Norway rat) 117033 Mmp12 mutant phenotype evidence used in manual assertion
  • PMID:12626598
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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: December 8, 2025