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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 10751 - 10775 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0080560 congenital disorder of glycosylation Ih Xenbase:XB-GENE-967053 Xenopus laevis (African clawed frog) 431849 alg8.S
  • MGI:6194238
DOID:0050770 polycystic liver disease Xenbase:XB-GENE-967053 Xenopus laevis (African clawed frog) 431849 alg8.S
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I Xenbase:XB-GENE-6036140 Xenopus tropicalis (tropical clawed frog) 100497477 alg9
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I ZFIN:ZDB-GENE-040426-1270 Danio rerio (zebrafish) 393598 alg9
  • MGI:6194238
DOID:0080564 congenital disorder of glycosylation Il Xenbase:XB-GENE-6036140 Xenopus tropicalis (tropical clawed frog) 100497477 alg9
  • MGI:6194238
DOID:0080564 congenital disorder of glycosylation Il ZFIN:ZDB-GENE-040426-1270 Danio rerio (zebrafish) 393598 alg9
  • MGI:6194238
DOID:0080564 congenital disorder of glycosylation Il Xenbase:XB-GENE-6486179 Xenopus laevis (African clawed frog) 108696484 alg9.L
  • MGI:6194238
DOID:0080563 congenital disorder of glycosylation Ik WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00020820 Caenorhabditis elegans 175920 algn-1
  • MGI:6194238
DOID:0110645 long QT syndrome 2 WB:WBGene00007043 Caenorhabditis elegans 172855 algn-10
  • MGI:6194238
DOID:0050563 nonsyndromic deafness WB:WBGene00007043 Caenorhabditis elegans 172855 algn-10
  • MGI:6194238
DOID:0080567 congenital disorder of glycosylation Ip WB:WBGene00015162 Caenorhabditis elegans 176032 algn-11
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00022629 Caenorhabditis elegans 179185 algn-12
  • MGI:6194238
DOID:0080559 congenital disorder of glycosylation Ig WB:WBGene00022629 Caenorhabditis elegans 179185 algn-12
  • MGI:6194238
DOID:0080470 developmental and epileptic encephalopathy 36 WB:WBGene00011193 Caenorhabditis elegans 179890 algn-13
  • MGI:6194238
DOID:0110658 congenital myasthenic syndrome 15 WB:WBGene00019725 Caenorhabditis elegans 187398 algn-14
  • MGI:6194238
DOID:0110669 congenital myasthenic syndrome 14 WB:WBGene00017282 Caenorhabditis elegans 173912 algn-2
  • MGI:6194238
DOID:0080561 congenital disorder of glycosylation Ii WB:WBGene00017282 Caenorhabditis elegans 173912 algn-2
  • MGI:6194238
DOID:5212 congenital disorder of glycosylation WB:WBGene00010720 Caenorhabditis elegans 175065 algn-3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id WB:WBGene00010720 Caenorhabditis elegans 175065 algn-3
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00019276 Caenorhabditis elegans 178822 algn-5
  • MGI:6194238
DOID:0080322 polycystic kidney disease WB:WBGene00019276 Caenorhabditis elegans 178822 algn-5
  • MGI:6194238
DOID:0050570 congenital disorder of glycosylation type I WB:WBGene00007435 Caenorhabditis elegans 182392 algn-6
  • MGI:6194238
DOID:0080555 congenital disorder of glycosylation Ic WB:WBGene00007435 Caenorhabditis elegans 182392 algn-6
  • 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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Last updated: August 19, 2024