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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 5401 - 5425 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050570 congenital disorder of glycosylation type I RGD:1305468 Rattus norvegicus (Norway rat) 293129 Alg8
  • MGI:6194238
DOID:0080560 congenital disorder of glycosylation Ih RGD:1305468 Rattus norvegicus (Norway rat) 293129 Alg8
  • MGI:6194238
DOID:2871 endometrial carcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:27050373
DOID:11446 sciatic neuropathy HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:219 colon cancer HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:9408 acute myocardial infarction HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:303 substance-related disorder HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:0050866 oral squamous cell carcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21393552
DOID:5844 myocardial infarction HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:90 degenerative disc disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:29393545
DOID:3525 middle cerebral artery infarction HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:332 amyotrophic lateral sclerosis HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:12675919
DOID:8725 vascular dementia HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:1824 status epilepticus HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:3312 bipolar disorder HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:16397405
  • PMID:17357145
DOID:10763 hypertension HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:0050850 diabetic encephalopathy HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
  • PMID:19154537
  • PMID:24101602
DOID:5419 schizophrenia HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
  • PMID:14745448
  • PMID:15254796
  • PMID:16397405
DOID:0050861 colorectal adenocarcinoma HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • PMID:21609933
DOID:14330 Parkinson's disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:114 heart disease HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:1596 depressive disorder HGNC:4617 Homo sapiens (human) 2932 GSK3B
  • MGI:6194238
DOID:3908 lung non-small cell carcinoma RGD:727787 Rattus norvegicus (Norway rat) 293451 Hs3st2
  • 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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Last updated: August 19, 2024