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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 4326 - 4350 of 12216 in total
Disease ID ▼ Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:326 ischemia HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:3213 demyelinating disease HGNC:9605 Homo sapiens (human) 5743 PTGS2
  • PMID:14694045
DOID:3213 demyelinating disease MGI:97250 Mus musculus (house mouse) 17869 Myc
  • MGI:6194238
DOID:3213 demyelinating disease RGD:3130 Rattus norvegicus (Norway rat) 24577 Myc
  • MGI:6194238
DOID:3211 lysosomal storage disease FB:FBgn0041630 Drosophila melanogaster (fruit fly) 38528 Hexo1 CG1318
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:318 Homo sapiens (human) 175 AGA
  • PMID:1703489
DOID:3211 lysosomal storage disease FB:FBgn0045063 Drosophila melanogaster (fruit fly) 250735 fdl CG8824
  • MGI:6194238
DOID:3211 lysosomal storage disease WB:WBGene00020509 Caenorhabditis elegans 180533 hex-1
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:9498 Homo sapiens (human) 5660 PSAP
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:4296 Homo sapiens (human) 2717 GLA
  • MGI:6194238
DOID:3211 lysosomal storage disease RGD:1307607 Rattus norvegicus (Norway rat) 294673 Hexb
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:9251 Homo sapiens (human) 5476 CTSA
  • PMID:8514852
DOID:3211 lysosomal storage disease MGI:96074 Mus musculus (house mouse) 15212 Hexb
  • MGI:6194238
DOID:3211 lysosomal storage disease FB:FBgn0041629 Drosophila melanogaster (fruit fly) 31808 Hexo2 CG1787
  • MGI:6194238
DOID:3211 lysosomal storage disease HGNC:4879 Homo sapiens (human) 3074 HEXB
  • MGI:6194238
DOID:321 tropical spastic paraparesis HGNC:18788 Homo sapiens (human) 22914 KLRK1
  • PMID:22170554
DOID:3181 oligodendroglioma RGD:1561913 Rattus norvegicus (Norway rat) 362809 Ptges3
  • MGI:6194238
DOID:3181 oligodendroglioma HGNC:16049 Homo sapiens (human) 10728 PTGES3
  • PMID:19347995
DOID:3181 oligodendroglioma MGI:1929282 Mus musculus (house mouse) 56351 Ptges3
  • MGI:6194238
DOID:3178 skin papilloma HGNC:11848 Homo sapiens (human) 7097 TLR2
  • PMID:24617037
DOID:3178 skin papilloma MGI:1346060 Mus musculus (house mouse) 24088 Tlr2
  • MGI:6194238
DOID:3153 lipomatosis HGNC:1848 Homo sapiens (human) 1056 CEL
  • PMID:17259390
DOID:3146 lipid metabolism disorder HGNC:2859 Homo sapiens (human) 1718 DHCR24
  • PMID:11519011
DOID:3146 lipid metabolism disorder HGNC:5213 Homo sapiens (human) 3295 HSD17B4
  • 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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