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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 8276 - 8300 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:13359 Ehlers-Danlos syndrome RGD:1309214 Rattus norvegicus (Norway rat) 364675 B4galt7
  • MGI:6194238
DOID:0080738 Ehlers-Danlos syndrome spondylodysplastic type 1 RGD:1309214 Rattus norvegicus (Norway rat) 364675 B4galt7
  • MGI:6194238
DOID:0090075 hypogonadotropic hypogonadism 15 with or without anosmia RGD:1309218 Rattus norvegicus (Norway rat) 316325 Hs6st1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome RGD:1309356 Rattus norvegicus (Norway rat) 299841 Rxylt1
  • MGI:6194238
DOID:0111239 congenital muscular dystrophy-dystroglycanopathy type A10 RGD:1309356 Rattus norvegicus (Norway rat) 299841 Rxylt1
  • MGI:6194238
DOID:0070433 hyperphosphatasia with impaired intellectual development syndrome 1 RGD:1309526 Rattus norvegicus (Norway rat) 366478 Pigv
  • MGI:6194238
DOID:0050588 muscular dystrophy-dystroglycanopathy type B1 RGD:1309541 Rattus norvegicus (Norway rat) 293667 B4gat1
  • MGI:6194238
DOID:0111238 congenital muscular dystrophy-dystroglycanopathy type A13 RGD:1309541 Rattus norvegicus (Norway rat) 293667 B4gat1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome RGD:1309541 Rattus norvegicus (Norway rat) 293667 B4gat1
  • MGI:6194238
DOID:0050802 Ehlers-Danlos syndrome spondylodysplastic type 2 RGD:1309558 Rattus norvegicus (Norway rat) 298690 B3galt6
  • MGI:6194238
DOID:13359 Ehlers-Danlos syndrome RGD:1309558 Rattus norvegicus (Norway rat) 298690 B3galt6
  • MGI:6194238
DOID:0112198 spondyloepimetaphyseal dysplasia with joint laxity type 1 RGD:1309558 Rattus norvegicus (Norway rat) 298690 B3galt6
  • MGI:6194238
DOID:206 hereditary multiple exostoses RGD:1309572 Rattus norvegicus (Norway rat) 313610 Extl1
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 RGD:1309940 Rattus norvegicus (Norway rat) 313231 Alg2
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii RGD:1309940 Rattus norvegicus (Norway rat) 313231 Alg2
  • MGI:6194238
DOID:2377 multiple sclerosis RGD:1310062 Rattus norvegicus (Norway rat) 362275 B4galt5
  • 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
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

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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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