Table Filtering
Other Information
Release Statistics Download
Guidelines
MIRAGE
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 9926 - 9950 of 14279 in total
Disease ID Disease Name ▲ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence References
DOID:0050908 myelodysplastic syndrome HGNC:4396 Homo sapiens (human) 2782 GNB1 inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:0050908 myelodysplastic syndrome MGI:1206586 Mus musculus (house mouse) 104416 Bap1 author statement supported by traceable reference
  • PMID:22878500
DOID:0050908 myelodysplastic syndrome HGNC:7989 Homo sapiens (human) 4893 NRAS inference by association of genotype from phenotype used in manual assertion
  • PMID:23708912
DOID:0050908 myelodysplastic syndrome HGNC:23019 Homo sapiens (human) 8233 ZRSR2 inference by association of genotype from phenotype used in manual assertion
  • PMID:22343920
  • PMID:25586593
  • PMID:28220884
  • PMID:28942350
DOID:0050908 myelodysplastic syndrome HGNC:15917 Homo sapiens (human) 23236 PLCB1 direct assay evidence used in manual assertion
  • PMID:21109771
DOID:0050908 myelodysplastic syndrome HGNC:25941 Homo sapiens (human) 54790 TET2 inference by association of genotype from phenotype used in manual assertion
  • PMID:20693430
  • PMID:23099237
  • RGD:7240710
DOID:0050908 myelodysplastic syndrome HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:12624489
DOID:0050908 myelodysplastic syndrome HGNC:11998 Homo sapiens (human) 7157 TP53 inference by association of genotype from phenotype used in manual assertion
  • PMID:24836762
  • PMID:25573287
DOID:0050908 myelodysplastic syndrome MGI:2684063 Mus musculus (house mouse) 228790 Asxl1 author statement supported by traceable reference
  • PMID:24218140
  • PMID:24255920
  • PMID:29113963
DOID:0050908 myelodysplastic syndrome HGNC:10783 Homo sapiens (human) 6427 SRSF2 inference by association of genotype from phenotype used in manual assertion
  • PMID:23280334
DOID:4972 myelodysplastic/myeloproliferative neoplasm MGI:1344352 Mus musculus (house mouse) 23856 Dido1 author statement supported by traceable reference
  • PMID:16127461
DOID:4971 myelofibrosis MGI:1337080 Mus musculus (house mouse) 20602 Ncor2 author statement supported by traceable reference
  • PMID:24191050
DOID:4971 myelofibrosis HGNC:1455 Homo sapiens (human) 811 CALR inference by association of genotype from phenotype used in manual assertion
  • PMID:24997152
  • PMID:25860380
  • RGD:7240710
DOID:4971 myelofibrosis HGNC:7217 Homo sapiens (human) 4352 MPL inference by association of genotype from phenotype used in manual assertion
  • RGD:7240710
DOID:4971 myelofibrosis HGNC:3527 Homo sapiens (human) 2146 EZH2 inference by association of genotype from phenotype used in manual assertion
  • PMID:21921040
DOID:4971 myelofibrosis MGI:97249 Mus musculus (house mouse) 17863 Myb author statement supported by traceable reference
  • PMID:20610815
DOID:4971 myelofibrosis HGNC:7132 Homo sapiens (human) 4297 KMT2A inference by association of genotype from phenotype used in manual assertion
  • PMID:35731275
DOID:4971 myelofibrosis HGNC:18318 Homo sapiens (human) 171023 ASXL1 inference by association of genotype from phenotype used in manual assertion
  • PMID:21712540
  • PMID:23619563
DOID:4971 myelofibrosis HGNC:4886 Homo sapiens (human) 3077 HFE inference by association of genotype from phenotype used in manual assertion
  • PMID:19258483
DOID:8692 myeloid leukemia HGNC:12767 Homo sapiens (human) 54904 NSD3 inference by association of genotype from phenotype used in manual assertion
  • PMID:11986249
DOID:8692 myeloid leukemia HGNC:12530 Homo sapiens (human) 54658 UGT1A1 inference by association of genotype from phenotype used in manual assertion
  • PMID:23609856
DOID:8692 myeloid leukemia HGNC:3688 Homo sapiens (human) 2260 FGFR1 mutant phenotype evidence used in manual assertion
  • PMID:19506298
DOID:8692 myeloid leukemia HGNC:5438 Homo sapiens (human) 3458 IFNG inference by association of genotype from phenotype used in manual assertion
  • PMID:20959405
DOID:8692 myeloid leukemia HGNC:7180 Homo sapiens (human) 4330 MN1 inference by association of genotype from phenotype used in manual assertion
  • PMID:7731705
DOID:8692 myeloid leukemia HGNC:8803 Homo sapiens (human) 5156 PDGFRA mutant phenotype evidence used in manual assertion
  • PMID:24486648

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.2.1

Last updated: April 7, 2025