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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 26 - 50 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▼ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:14264 benign neonatal seizures MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:0050635 alternating hemiplegia of childhood MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:1574 alcohol use disorder MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:10763 hypertension MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:1826 epilepsy MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:0111182 familial hemiplegic migraine 2 MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
  • PMID:21731499
  • PMID:26911348
DOID:9279 hyperhomocysteinemia MGI:88106 Mus musculus (house mouse) 98660 Atp1a2
  • MGI:6194238
DOID:0111507 Lenz-Majewski hyperostotic dwarfism HGNC:9587 Homo sapiens (human) 9791 PTDSS1
  • RGD:7240710
DOID:0111230 congenital muscular dystrophy-dystroglycanopathy type A11 MGI:2145517 Mus musculus (house mouse) 97884 B3galnt2
  • MGI:6194238
DOID:1485 cystic fibrosis HGNC:18967 Homo sapiens (human) 9695 EDEM1
  • MGI:6194238
DOID:9970 obesity HGNC:10660 Homo sapiens (human) 9672 SDC3
  • RGD:7240710
DOID:0080108 myoglobinuria HGNC:14450 Homo sapiens (human) 9663 LPIN2
  • MGI:6194238
DOID:3146 lipid metabolism disorder HGNC:14450 Homo sapiens (human) 9663 LPIN2
  • MGI:6194238
DOID:9970 obesity HGNC:14450 Homo sapiens (human) 9663 LPIN2
  • MGI:6194238
DOID:10283 prostate cancer HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:17998819
DOID:3008 invasive ductal carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:17059779
DOID:5138 leiomyomatosis HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:15762960
DOID:0050861 colorectal adenocarcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:16425351
DOID:3007 breast ductal carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:16425351
DOID:3717 gastric adenocarcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:16425351
DOID:5154 borna disease HGNC:1681 Homo sapiens (human) 960 CD44
  • MGI:6194238
DOID:4450 renal cell carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:12833185
  • PMID:17284111
DOID:3910 lung adenocarcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:18091389
  • PMID:29537891
DOID:13580 cholestasis HGNC:1681 Homo sapiens (human) 960 CD44
  • MGI:6194238
DOID:9597 Krukenberg carcinoma HGNC:1681 Homo sapiens (human) 960 CD44
  • PMID:16124061

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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