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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 66251 - 66275 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1064 cystinosis WB:WBGene00008052 Caenorhabditis elegans 174308 ctns-1
  • MGI:6194238
  • PMID:22822152
DOID:0111458 galactose epimerase deficiency WB:WBGene00008132 Caenorhabditis elegans 173171 gale-1
  • MGI:6194238
DOID:9870 galactosemia WB:WBGene00008132 Caenorhabditis elegans 173171 gale-1
  • MGI:6194238
  • PMID:25298520
DOID:1588 thrombocytopenia WB:WBGene00008132 Caenorhabditis elegans 173171 gale-1
  • MGI:6194238
DOID:1485 cystic fibrosis WB:WBGene00008148 Caenorhabditis elegans 177857 C47E12.3
  • MGI:6194238
DOID:2747 glycogen storage disease WB:WBGene00008230 Caenorhabditis elegans 179335 pfk-1.2
  • MGI:6194238
DOID:0014667 disease of metabolism WB:WBGene00008230 Caenorhabditis elegans 179335 pfk-1.2
  • MGI:6194238
DOID:11721 glycogen storage disease VII WB:WBGene00008230 Caenorhabditis elegans 179335 pfk-1.2
  • MGI:6194238
DOID:2962 Cockayne syndrome WB:WBGene00008403 Caenorhabditis elegans 174474 csa-1
  • MGI:6194238
  • PMID:25453470
DOID:0060240 UV-sensitive syndrome WB:WBGene00008403 Caenorhabditis elegans 174474 csa-1
  • MGI:6194238
DOID:0080907 Cockayne syndrome A WB:WBGene00008403 Caenorhabditis elegans 174474 csa-1
  • MGI:6194238
DOID:0112315 brain small vessel disease 3 WB:WBGene00008426 Caenorhabditis elegans 3565069 D2045.9
  • MGI:6194238
DOID:0080139 multiple congenital anomalies-hypotonia-seizures syndrome 2 WB:WBGene00008431 Caenorhabditis elegans 174386 piga-1
  • MGI:6194238
DOID:0060284 paroxysmal nocturnal hemoglobinuria WB:WBGene00008431 Caenorhabditis elegans 174386 piga-1
  • MGI:6194238
DOID:0060713 autosomal recessive congenital ichthyosis 4B WB:WBGene00008431 Caenorhabditis elegans 174386 piga-1
  • MGI:6194238
DOID:783 end stage renal disease WB:WBGene00008542 Caenorhabditis elegans 184107 scav-6
  • MGI:6194238
DOID:891 progressive myoclonus epilepsy WB:WBGene00008542 Caenorhabditis elegans 184107 scav-6
  • MGI:6194238
DOID:0111019 cone-rod dystrophy 12 WB:WBGene00008571 Caenorhabditis elegans 181330 prmn-1
  • MGI:6194238
DOID:0070517 retinal macular dystrophy 2 WB:WBGene00008571 Caenorhabditis elegans 181330 prmn-1
  • MGI:6194238
DOID:0110376 retinitis pigmentosa 41 WB:WBGene00008571 Caenorhabditis elegans 181330 prmn-1
  • MGI:6194238
DOID:9351 diabetes mellitus WB:WBGene00008571 Caenorhabditis elegans 181330 prmn-1
  • MGI:6194238
DOID:1681 heart septal defect WB:WBGene00008624 Caenorhabditis elegans 178267 crld-1
  • MGI:6194238
DOID:0050651 atrioventricular septal defect WB:WBGene00008624 Caenorhabditis elegans 178267 crld-1
  • MGI:6194238
DOID:1793 pancreatic cancer WB:WBGene00008656 Caenorhabditis elegans 184307 lron-5
  • MGI:6194238
DOID:11342 arcus senilis WB:WBGene00008656 Caenorhabditis elegans 184307 lron-5
  • 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