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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 7751 - 7775 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:1574 alcohol use disorder HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:30277635
DOID:0080552 congenital disorder of glycosylation Ia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19207313
DOID:12217 Lewy body dementia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19276553
DOID:3594 choriocarcinoma HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:17556377
DOID:635 acquired immunodeficiency syndrome HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:11232005
DOID:11476 osteoporosis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:14330 Parkinson's disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:19276553
DOID:9744 type 1 diabetes mellitus HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:24685003
DOID:14681 Silver-Russell syndrome HGNC:5466 Homo sapiens (human) 3481 IGF2
  • RGD:7240710
DOID:684 hepatocellular carcinoma HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:16750516
DOID:14183 alcoholic neuropathy HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:0050589 inflammatory bowel disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
  • PMID:12548059
DOID:3827 congenital diaphragmatic hernia HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:4752 multiple system atrophy HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:20683839
DOID:9352 type 2 diabetes mellitus HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:77 gastrointestinal system disease HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:16477536
DOID:9471 meningitis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:7521338
DOID:3454 brain infarction HGNC:5466 Homo sapiens (human) 3481 IGF2
  • MGI:6194238
DOID:8577 ulcerative colitis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:16088202
DOID:0081312 T-cell non-Hodgkin lymphoma HGNC:5392 Homo sapiens (human) 8870 IER3
  • PMID:14534530
DOID:12802 mucopolysaccharidosis I HGNC:5391 Homo sapiens (human) 3425 IDUA
  • MGI:6194238
  • PMID:11172140
  • PMID:12948739
  • PMID:1301196
  • PMID:1301941
  • PMID:15126990
  • PMID:15128896
  • PMID:15194053
  • PMID:16435195
  • PMID:16860035
  • PMID:17407189
  • PMID:17606547
  • PMID:18523448
  • PMID:21734815
  • PMID:24100243
  • PMID:25597593
  • PMID:27146977
  • PMID:7951228
  • PMID:8664897
DOID:0111390 mucopolysaccharidosis Ih HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:0111389 mucopolysaccharidosis Ih/s HGNC:5391 Homo sapiens (human) 3425 IDUA
  • RGD:7240710
DOID:10754 otitis media HGNC:5391 Homo sapiens (human) 3425 IDUA
  • 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