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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 68801 - 68825 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10763 hypertension RGD:620630 Rattus norvegicus (Norway rat) 85268 Hrh3
  • PMID:9050021
DOID:1508 candidiasis SGD:S000003149 Saccharomyces cerevisiae S288C 852694 GTS1
  • MGI:6194238
DOID:0050561 Lennox-Gastaut syndrome HGNC:2851 Homo sapiens (human) 8527 DGKD
  • MGI:6194238
DOID:10652 Alzheimer's disease SGD:S000003141 Saccharomyces cerevisiae S288C 852702 XRN1
  • MGI:6194238
DOID:10112 sleeping sickness SGD:S000003110 Saccharomyces cerevisiae S288C 852735 GPI10
  • PMID:10954751
DOID:0112216 developmental and epileptic encephalopathy 80 SGD:S000003110 Saccharomyces cerevisiae S288C 852735 GPI10
  • MGI:6194238
DOID:9119 acute myeloid leukemia SGD:S000003060 Saccharomyces cerevisiae S288C 852788 NUP145
  • PMID:29034209
DOID:5603 T-cell acute lymphoblastic leukemia SGD:S000003060 Saccharomyces cerevisiae S288C 852788 NUP145
  • MGI:6194238
DOID:0060644 chondrodysplasia-pseudohermaphroditism syndrome SGD:S000003052 Saccharomyces cerevisiae S288C 852796 GUP1
  • MGI:6194238
DOID:0080980 arthrogryposis multiplex congenita-4 SGD:S000003051 Saccharomyces cerevisiae S288C 852797 SCY1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease SGD:S000003045 Saccharomyces cerevisiae S288C 852803 HNM1
  • MGI:6194238
DOID:0111666 proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome SGD:S000003045 Saccharomyces cerevisiae S288C 852803 HNM1
  • PMID:38302740
DOID:9455 lipid storage disease SGD:S000003045 Saccharomyces cerevisiae S288C 852803 HNM1
  • MGI:6194238
DOID:12858 Huntington's disease SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:11383 cryptorchidism SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:83 cataract SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:10652 Alzheimer's disease SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:0110255 cataract 5 multiple types SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:14330 Parkinson's disease SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:6000 congestive heart failure SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:224 transient cerebral ischemia SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:767 muscular atrophy SGD:S000003041 Saccharomyces cerevisiae S288C 852806 HSF1
  • MGI:6194238
DOID:0112113 combined oxidative phosphorylation deficiency 45 SGD:S000003036 Saccharomyces cerevisiae S288C 852811 MNP1
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii SGD:S000003033 Saccharomyces cerevisiae S288C 852815 ALG2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 SGD:S000003033 Saccharomyces cerevisiae S288C 852815 ALG2
  • 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