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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 3901 - 3925 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10908 hydrocephalus RGD:1310810 Rattus norvegicus (Norway rat) 306549 Pomk
  • MGI:6194238
DOID:0112381 muscular dystrophy-dystroglycanopathy type C12 RGD:1310810 Rattus norvegicus (Norway rat) 306549 Pomk
  • MGI:6194238
DOID:0111235 congenital muscular dystrophy-dystroglycanopathy type A12 RGD:1310810 Rattus norvegicus (Norway rat) 306549 Pomk
  • MGI:6194238
DOID:10652 Alzheimer's disease RGD:1310764 Rattus norvegicus (Norway rat) 309465 Gsto2
  • MGI:6194238
DOID:14330 Parkinson's disease RGD:1310764 Rattus norvegicus (Norway rat) 309465 Gsto2
  • MGI:6194238
DOID:2841 asthma RGD:1310764 Rattus norvegicus (Norway rat) 309465 Gsto2
  • MGI:6194238
DOID:1574 alcohol use disorder RGD:1310764 Rattus norvegicus (Norway rat) 309465 Gsto2
  • MGI:6194238
DOID:0080563 congenital disorder of glycosylation Ik RGD:1310700 Rattus norvegicus (Norway rat) 360475 Alg1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I RGD:1310700 Rattus norvegicus (Norway rat) 360475 Alg1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation RGD:1310700 Rattus norvegicus (Norway rat) 360475 Alg1
  • MGI:6194238
DOID:0050571 congenital disorder of glycosylation type II RGD:1310692 Rattus norvegicus (Norway rat) 292090 Galnt2
  • MGI:6194238
DOID:12858 Huntington's disease RGD:1310309 Rattus norvegicus (Norway rat) 293504 Qprt
  • PMID:2527078
DOID:0080557 congenital disorder of glycosylation Ie RGD:1310120 Rattus norvegicus (Norway rat) 296394 Dpm1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I RGD:1310120 Rattus norvegicus (Norway rat) 296394 Dpm1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:9884 muscular dystrophy RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0050559 Fukuyama congenital muscular dystrophy RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0110444 dilated cardiomyopathy 1X RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0110443 dilated cardiomyopathy 1B RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:1289 neurodegenerative disease RGD:1310078 Rattus norvegicus (Norway rat) 287545 Sarm1
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis RGD:1310078 Rattus norvegicus (Norway rat) 287545 Sarm1
  • 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