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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 4026 - 4050 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References ▲
DOID:0090117 thiamine-responsive megaloblastic anemia syndrome WB:WBGene00018138 Caenorhabditis elegans 178745 folt-2 sequence orthology evidence used in manual assertion
  • PMID:17475669
DOID:3347 osteosarcoma HGNC:8824 Homo sapiens (human) 5176 SERPINF1 mutant phenotype evidence used in manual assertion
  • PMID:17479108
DOID:1612 breast cancer HGNC:8590 Homo sapiens (human) 5058 PAK1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17486065
DOID:2871 endometrial carcinoma HGNC:11219 Homo sapiens (human) 6678 SPARC direct assay evidence used in manual assertion
  • PMID:17487382
DOID:12894 Sjogren's syndrome HGNC:4944 Homo sapiens (human) 3119 HLA-DQB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17489060
  • PMID:21315052
  • PMID:8468491
DOID:12185 otosclerosis HGNC:2197 Homo sapiens (human) 1277 COL1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17489845
DOID:10283 prostate cancer HGNC:12828 Homo sapiens (human) 7515 XRCC1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17491266
DOID:9970 obesity HGNC:8824 Homo sapiens (human) 5176 SERPINF1 direct assay evidence used in manual assertion
  • PMID:17491674
DOID:1909 melanoma HGNC:7794 Homo sapiens (human) 4790 NFKB1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17492467
DOID:3021 acute kidney failure RGD:3371 Rattus norvegicus (Norway rat) 25664 Pparg direct assay evidence used in manual assertion
  • PMID:17494862
DOID:2316 brain ischemia RGD:621861 Rattus norvegicus (Norway rat) 89805 Angpt2 direct assay evidence used in manual assertion
  • PMID:17494864
DOID:9970 obesity HGNC:2228 Homo sapiens (human) 1312 COMT inference by association of genotype from phenotype used in manual assertion
  • PMID:17497175
DOID:1273 respiratory syncytial virus infectious disease HGNC:10801 Homo sapiens (human) 6439 SFTPB inference by association of genotype from phenotype used in manual assertion
  • PMID:17498296
DOID:6000 congestive heart failure MGI:1917258 Mus musculus (house mouse) 70008 Ace2 author statement supported by traceable reference
  • PMID:17499227
DOID:13375 temporal arteritis HGNC:7176 Homo sapiens (human) 4318 MMP9 direct assay evidence used in manual assertion
  • PMID:17502363
DOID:13375 temporal arteritis HGNC:7166 Homo sapiens (human) 4313 MMP2 direct assay evidence used in manual assertion
  • PMID:17502363
DOID:2044 drug-induced hepatitis HGNC:53 Homo sapiens (human) 1244 ABCC2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17502832
DOID:1485 cystic fibrosis HGNC:286 Homo sapiens (human) 154 ADRB2 inference by association of genotype from phenotype used in manual assertion
  • PMID:17502834
DOID:9074 systemic lupus erythematosus HGNC:1324 Homo sapiens (human) 721 C4B inference by association of genotype from phenotype used in manual assertion
  • PMID:17503323
DOID:9074 systemic lupus erythematosus HGNC:1323 Homo sapiens (human) 720 C4A inference by association of genotype from phenotype used in manual assertion
  • PMID:17503323
DOID:0110569 autosomal dominant nonsyndromic deafness 44 HGNC:18111 Homo sapiens (human) 152137 CCDC50 inference by association of genotype from phenotype used in manual assertion
  • PMID:17503326
  • RGD:7240710
DOID:0050753 cerebellar ataxia HGNC:17089 Homo sapiens (human) 23345 SYNE1 inference by association of genotype from phenotype used in manual assertion
  • PMID:17503513
DOID:127 leiomyoma RGD:3852 Rattus norvegicus (Norway rat) 29591 Tgfbr1 mutant phenotype evidence used in manual assertion
  • PMID:17505012
DOID:0050811 congenital adrenal hyperplasia HGNC:9208 Homo sapiens (human) 5447 POR inference by association of genotype from phenotype used in manual assertion
  • PMID:17505056
DOID:2913 acute pancreatitis HGNC:3544 Homo sapiens (human) 2155 F7 direct assay evidence used in manual assertion
  • PMID:17506000

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

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