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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 2501 - 2525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:11723 Duchenne muscular dystrophy FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0050453 lissencephaly FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
  • PMID:25232965
DOID:0110278 autosomal recessive limb-girdle muscular dystrophy type 2D FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0111232 congenital muscular dystrophy-dystroglycanopathy type A9 FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • PMID:36634851
DOID:9352 type 2 diabetes mellitus FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:11650 bronchopulmonary dysplasia FB:FBgn0034072 Drosophila melanogaster (fruit fly) 36773 Dg CG18250
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:10787 premature menopause MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:9452 steatotic liver disease RGD:620329 Rattus norvegicus (Norway rat) 252900 Dgat2
  • PMID:17526931
DOID:0080208 metabolic dysfunction-associated steatotic liver disease RGD:620329 Rattus norvegicus (Norway rat) 252900 Dgat2
  • MGI:6194238
  • PMID:24166662
  • PMID:26394137
DOID:9452 steatotic liver disease MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:784 chronic kidney disease RGD:620329 Rattus norvegicus (Norway rat) 252900 Dgat2
  • PMID:23045433
DOID:784 chronic kidney disease MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:10787 premature menopause RGD:620329 Rattus norvegicus (Norway rat) 252900 Dgat2
  • PMID:25263431
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria RGD:1308092 Rattus norvegicus (Norway rat) 361272 Dhtkd1
  • MGI:6194238
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q MGI:2445096 Mus musculus (house mouse) 209692 Dhtkd1
  • MGI:6194238
  • PMID:29661920
  • PMID:32169121
DOID:0111453 2-aminoadipic 2-oxoadipic aciduria MGI:2445096 Mus musculus (house mouse) 209692 Dhtkd1
  • MGI:6194238
  • PMID:28545977
DOID:0110170 Charcot-Marie-Tooth disease axonal type 2Q RGD:1308092 Rattus norvegicus (Norway rat) 361272 Dhtkd1
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency RGD:619859 Rattus norvegicus (Norway rat) 81654 Dlat
  • MGI:6194238
DOID:3650 lactic acidosis MGI:2385311 Mus musculus (house mouse) 235339 Dlat
  • MGI:6194238
DOID:3650 lactic acidosis RGD:619859 Rattus norvegicus (Norway rat) 81654 Dlat
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency MGI:2385311 Mus musculus (house mouse) 235339 Dlat
  • 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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