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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 11001 - 11025 of 12216 in total
Disease ID Disease Name ▼ Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0080037 Worth syndrome MGI:1278315 Mus musculus (house mouse) 16973 Lrp5
  • MGI:6194238
DOID:0080037 Worth syndrome HGNC:6697 Homo sapiens (human) 4041 LRP5
  • RGD:7240710
DOID:14497 Wolman disease MGI:96789 Mus musculus (house mouse) 16889 Lipa
  • MGI:6194238
  • PMID:9700186
DOID:14497 Wolman disease HGNC:6617 Homo sapiens (human) 3988 LIPA
  • MGI:6194238
  • PMID:6097111
  • PMID:8146180
  • RGD:7240710
DOID:384 Wolff-Parkinson-White syndrome HGNC:9386 Homo sapiens (human) 51422 PRKAG2
  • MGI:6194238
  • PMID:11748095
  • PMID:15611370
  • RGD:7240710
DOID:384 Wolff-Parkinson-White syndrome MGI:1891343 Mus musculus (house mouse) 241113 Prkag3
  • MGI:6194238
DOID:384 Wolff-Parkinson-White syndrome MGI:1336153 Mus musculus (house mouse) 108099 Prkag2
  • MGI:6194238
DOID:384 Wolff-Parkinson-White syndrome HGNC:9387 Homo sapiens (human) 53632 PRKAG3
  • MGI:6194238
DOID:893 Wilson disease WB:WBGene00000213 Caenorhabditis elegans 176879 asm-3
  • MGI:6194238
DOID:893 Wilson disease MGI:98325 Mus musculus (house mouse) 20597 Smpd1
  • MGI:6194238
DOID:893 Wilson disease WB:WBGene00000212 Caenorhabditis elegans 181323 asm-2
  • MGI:6194238
DOID:893 Wilson disease HGNC:543 Homo sapiens (human) 308 ANXA5
  • MGI:6194238
DOID:893 Wilson disease WB:WBGene00000211 Caenorhabditis elegans 174131 asm-1
  • MGI:6194238
DOID:893 Wilson disease HGNC:2606 Homo sapiens (human) 1594 CYP27B1
  • MGI:6194238
DOID:893 Wilson disease HGNC:11120 Homo sapiens (human) 6609 SMPD1
  • MGI:6194238
DOID:0050562 West syndrome HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:2384 Wernicke encephalopathy HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • MGI:6194238
DOID:0050475 Weill-Marchesani syndrome MGI:104798 Mus musculus (house mouse) 21926 Tnf
  • MGI:6194238
DOID:0050475 Weill-Marchesani syndrome HGNC:11892 Homo sapiens (human) 7124 TNF
  • PMID:15223607
DOID:0050475 Weill-Marchesani syndrome RGD:3876 Rattus norvegicus (Norway rat) 24835 Tnf
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-1007367 Xenopus tropicalis (tropical clawed frog) 100170600 b4gat1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-944435 Xenopus tropicalis (tropical clawed frog) 448433 pomt1
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome Xenbase:XB-GENE-1006906 Xenopus tropicalis (tropical clawed frog) 100490100 pomt2
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome RGD:1305852 Rattus norvegicus (Norway rat) 308390 Fkrp
  • MGI:6194238
DOID:0050560 Walker-Warburg syndrome HGNC:15685 Homo sapiens (human) 11041 B4GAT1
  • MGI:6194238

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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