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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 October 9, 2024
Displaying entries 63201 - 63225 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:8501 fundus dystrophy WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:10976 membranous glomerulonephritis WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:4448 macular degeneration WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:684 hepatocellular carcinoma WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:0050817 Stargardt disease WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:10584 retinitis pigmentosa WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:10787 premature menopause WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:0060712 autosomal recessive congenital ichthyosis 4A WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:0080957 primary hypoalphalipoproteinemia 1 WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00000020 Caenorhabditis elegans 171782 abt-2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:10113 trypanosomiasis WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:543 dystonia WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:9470 bacterial meningitis WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:10763 hypertension WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:0050784 primary progressive multiple sclerosis WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:1826 epilepsy WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:10914 amnestic disorder WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:6088 acute stress disorder WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:10652 Alzheimer's disease WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:4247 coronary restenosis WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238
DOID:437 myasthenia gravis WB:WBGene00000035 Caenorhabditis elegans 181706 ace-1
  • MGI:6194238

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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 9, 2024