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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 4451 - 4475 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:8398 osteoarthritis HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:22527881
DOID:1612 breast cancer HGNC:5466 Homo sapiens (human) 3481 IGF2
  • PMID:18719053
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:3910 lung adenocarcinoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • MGI:6194238
DOID:3459 breast carcinoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:29940770
DOID:0060060 non-Hodgkin lymphoma HGNC:5467 Homo sapiens (human) 3482 IGF2R
  • PMID:29940770

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Supported by JST NBDC Grant Number JPMJND2204

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Last updated: August 19, 2024