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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 7076 - 7100 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14330 Parkinson's disease MGI:1915464 Mus musculus (house mouse) 68214 Gsto2
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency MGI:1915513 Mus musculus (house mouse) 68263 Pdhb
  • MGI:6194238
DOID:0110292 autosomal recessive limb-girdle muscular dystrophy type 2O MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
DOID:0050453 lissencephaly MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
  • PMID:16458488
  • PMID:19114101
  • PMID:23454088
DOID:0111236 congenital muscular dystrophy-dystroglycanopathy type A3 MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
DOID:0112378 muscular dystrophy-dystroglycanopathy type B3 MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • PMID:26306834
DOID:10584 retinitis pigmentosa MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
DOID:9884 muscular dystrophy MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
DOID:0080572 congenital disorder of glycosylation Iw MGI:1915542 Mus musculus (house mouse) 68292 Stt3b
  • MGI:6194238
DOID:0080573 congenital disorder of glycosylation Ix MGI:1915542 Mus musculus (house mouse) 68292 Stt3b
  • MGI:6194238
DOID:0112136 severe congenital neutropenia 4 MGI:1915651 Mus musculus (house mouse) 68401 G6pc3
  • MGI:6194238
DOID:5082 liver cirrhosis MGI:1916211 Mus musculus (house mouse) 68961 Phkg2
  • MGI:6194238
DOID:2747 glycogen storage disease MGI:1916211 Mus musculus (house mouse) 68961 Phkg2
  • MGI:6194238
DOID:0111043 glycogen storage disease IXc MGI:1916211 Mus musculus (house mouse) 68961 Phkg2
  • MGI:6194238
DOID:14250 Down syndrome MGI:1916863 Mus musculus (house mouse) 80294 Pofut2
  • MGI:6194238
DOID:0050424 familial adenomatous polyposis MGI:1917853 Mus musculus (house mouse) 70603 Mutyh
  • MGI:6194238
DOID:0080410 familial adenomatous polyposis 2 MGI:1917853 Mus musculus (house mouse) 70603 Mutyh
  • MGI:6194238
DOID:5517 stomach carcinoma MGI:1917853 Mus musculus (house mouse) 70603 Mutyh
  • MGI:6194238
DOID:10534 stomach cancer MGI:1917853 Mus musculus (house mouse) 70603 Mutyh
  • MGI:6194238
DOID:0070238 primary coenzyme Q10 deficiency 1 MGI:1919133 Mus musculus (house mouse) 71883 Coq2
  • MGI:6194238
DOID:0050730 coenzyme Q10 deficiency disease MGI:1919133 Mus musculus (house mouse) 71883 Coq2
  • MGI:6194238
DOID:4752 multiple system atrophy MGI:1919133 Mus musculus (house mouse) 71883 Coq2
  • MGI:6194238
DOID:10603 glucose intolerance MGI:1919133 Mus musculus (house mouse) 71883 Coq2
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024