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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 July 29, 2024
Displaying entries 11201 - 11225 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0080560 congenital disorder of glycosylation Ih RGD:1305468 Rattus norvegicus (Norway rat) 293129 Alg8
  • MGI:6194238
DOID:0110676 congenital myasthenic syndrome 13 FB:FBgn0032477 Drosophila melanogaster (fruit fly) 34711 Alg7 CG5287
  • MGI:6194238
DOID:0080562 congenital disorder of glycosylation Ij FB:FBgn0032477 Drosophila melanogaster (fruit fly) 34711 Alg7 CG5287
  • MGI:6194238
  • PMID:36166480
DOID:0080555 congenital disorder of glycosylation Ic MGI:2444031 Mus musculus (house mouse) 320438 Alg6
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I RGD:1308815 Rattus norvegicus (Norway rat) 362547 Alg6
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I MGI:2444031 Mus musculus (house mouse) 320438 Alg6
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic RGD:1308815 Rattus norvegicus (Norway rat) 362547 Alg6
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I RGD:1308900 Rattus norvegicus (Norway rat) 295051 Alg5
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I MGI:1913498 Mus musculus (house mouse) 66248 Alg5
  • MGI:6194238
DOID:0080322 polycystic kidney disease RGD:1308900 Rattus norvegicus (Norway rat) 295051 Alg5
  • MGI:6194238
DOID:0080322 polycystic kidney disease MGI:1913498 Mus musculus (house mouse) 66248 Alg5
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation FB:FBgn0011297 Drosophila melanogaster (fruit fly) 37754 Alg3 CG4084
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id RGD:1306004 Rattus norvegicus (Norway rat) 287983 Alg3
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation MGI:1098592 Mus musculus (house mouse) 208624 Alg3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id MGI:1098592 Mus musculus (house mouse) 208624 Alg3
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation RGD:1306004 Rattus norvegicus (Norway rat) 287983 Alg3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id FB:FBgn0011297 Drosophila melanogaster (fruit fly) 37754 Alg3 CG4084
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 MGI:1914731 Mus musculus (house mouse) 56737 Alg2
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii FB:FBgn0035401 Drosophila melanogaster (fruit fly) 38374 Alg2 CG1291
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii MGI:1914731 Mus musculus (house mouse) 56737 Alg2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 RGD:1309940 Rattus norvegicus (Norway rat) 313231 Alg2
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 FB:FBgn0035401 Drosophila melanogaster (fruit fly) 38374 Alg2 CG1291
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii RGD:1309940 Rattus norvegicus (Norway rat) 313231 Alg2
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 FB:FBgn0030645 Drosophila melanogaster (fruit fly) 32479 Alg14 CG6308
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 RGD:1312003 Rattus norvegicus (Norway rat) 362031 Alg14
  • 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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