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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 9326 - 9350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
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:0050559 Fukuyama congenital muscular dystrophy MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
  • PMID:15837576
  • PMID:19017726
  • PMID:22922256
DOID:0112379 muscular dystrophy-dystroglycanopathy type B4 RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
DOID:0110443 dilated cardiomyopathy 1B MGI:2179507 Mus musculus (house mouse) 246179 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:0050588 muscular dystrophy-dystroglycanopathy type B1 MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • PMID:19017726
  • PMID:23562821
DOID:9884 muscular dystrophy MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
DOID:0110284 autosomal recessive limb-girdle muscular dystrophy type 2L MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
DOID:0110444 dilated cardiomyopathy 1X RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0110296 autosomal recessive limb-girdle muscular dystrophy type 2M MGI:2179507 Mus musculus (house mouse) 246179 Fktn
  • MGI:6194238
DOID:0110443 dilated cardiomyopathy 1B RGD:1310087 Rattus norvegicus (Norway rat) 362520 Fktn
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:9884 muscular dystrophy RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:0110635 muscular dystrophy-dystroglycanopathy type B5 RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:11724 limb-girdle muscular dystrophy MGI:2447586 Mus musculus (house mouse) 243853 Fkrp
  • MGI:6194238
DOID:11724 limb-girdle muscular dystrophy RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:0110299 autosomal recessive limb-girdle muscular dystrophy type 2I RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:0111241 congenital muscular dystrophy-dystroglycanopathy type A5 RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:0111241 congenital muscular dystrophy-dystroglycanopathy type A5 MGI:2447586 Mus musculus (house mouse) 243853 Fkrp
  • MGI:6194238
DOID:0110635 muscular dystrophy-dystroglycanopathy type B5 MGI:2447586 Mus musculus (house mouse) 243853 Fkrp
  • MGI:6194238
  • PMID:20675713

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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: August 19, 2024