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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 9976 - 10000 of 14279 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence References
DOID:9256 colorectal cancer HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21926398
DOID:0080188 chronic myelomonocytic leukemia HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21339759
DOID:1324 lung cancer HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:19901851
DOID:3347 osteosarcoma HGNC:3527 Homo sapiens (human) 2146 EZH2 mutant phenotype evidence used in manual assertion
  • PMID:26265454
DOID:9119 acute myeloid leukemia HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23099237
DOID:4971 myelofibrosis HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21921040
DOID:0050861 colorectal adenocarcinoma HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21926398
DOID:0050866 oral squamous cell carcinoma HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:26807327
DOID:684 hepatocellular carcinoma HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24040354
DOID:0050908 myelodysplastic syndrome HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22869879
DOID:5176 renal Wilms' tumor HGNC:3527 Homo sapiens (human) 2146 EZH2 mutant phenotype evidence used in manual assertion
  • PMID:18467665
DOID:10534 stomach cancer HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22228224
DOID:6000 congestive heart failure HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:33779075
DOID:707 B-cell lymphoma HGNC:3527 Homo sapiens (human) 2146 EZH2 mutant phenotype evidence used in manual assertion
  • PMID:29456795
DOID:8761 acute megakaryocytic leukemia HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24056718
DOID:4947 cholangiocarcinoma HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:24179546
DOID:0110384 retinitis pigmentosa 25 HGNC:21555 Homo sapiens (human) 346007 EYS inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110440 dilated cardiomyopathy 1J HGNC:3522 Homo sapiens (human) 2070 EYA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0110542 autosomal dominant nonsyndromic deafness 10 HGNC:3522 Homo sapiens (human) 2070 EYA4 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:6000 congestive heart failure HGNC:3522 Homo sapiens (human) 2070 EYA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15735644
DOID:12930 dilated cardiomyopathy HGNC:3522 Homo sapiens (human) 2070 EYA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15735644
DOID:10003 sensorineural hearing loss HGNC:3522 Homo sapiens (human) 2070 EYA4 inference by association of genotype from phenotype used in manual assertion
  • PMID:15735644
DOID:206 hereditary multiple exostoses HGNC:3512 Homo sapiens (human) 2131 EXT1 inference by association of genotype from phenotype used in manual assertion
  • PMID:12490068
  • PMID:17767039
  • PMID:18330718
  • PMID:24297320
  • PMID:25421355
  • PMID:26839764
  • PMID:8981950
DOID:3371 chondrosarcoma HGNC:3512 Homo sapiens (human) 2131 EXT1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0112334 pontocerebellar hypoplasia type 1C HGNC:17035 Homo sapiens (human) 11340 EXOSC8 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: April 7, 2025