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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 5001 - 5025 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
  • PMID:29392078
DOID:0050156 idiopathic pulmonary fibrosis WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:1074 kidney failure WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:12858 Huntington's disease WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:10534 stomach cancer WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:3525 middle cerebral artery infarction WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:10952 nephritis WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:127 leiomyoma WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:417 autoimmune disease WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:8677 perinatal necrotizing enterocolitis WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:5154 borna disease WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:224 transient cerebral ischemia WB:WBGene00004049 Caenorhabditis elegans 266823 parp-1
  • MGI:6194238
DOID:1168 familial hyperlipidemia HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • MGI:6194238
DOID:9970 obesity HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • PMID:11118009
DOID:9352 type 2 diabetes mellitus HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • PMID:17574229
DOID:0110660 congenital myasthenic syndrome 12 HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • MGI:6194238
  • RGD:7240710
DOID:1440 Machado-Joseph disease HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • MGI:6194238
DOID:2018 hyperinsulinism HGNC:4241 Homo sapiens (human) 2673 GFPT1
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • MGI:6194238
DOID:3049 Churg-Strauss syndrome HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • PMID:9853108
DOID:2316 brain ischemia HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • MGI:6194238
DOID:11446 sciatic neuropathy HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • MGI:6194238
DOID:10487 Hirschsprung's disease HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • MGI:6194238
DOID:9810 polyarteritis nodosa HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • PMID:9853108
DOID:14766 renal agenesis HGNC:4243 Homo sapiens (human) 2674 GFRA1
  • RGD:7240710

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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