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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 4876 - 4900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:9352 type 2 diabetes mellitus HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
  • PMID:17065694
  • PMID:18439701
  • PMID:22215535
DOID:784 chronic kidney disease HGNC:6554 Homo sapiens (human) 3953 LEPR
  • MGI:6194238
DOID:11476 osteoporosis HGNC:6554 Homo sapiens (human) 3953 LEPR
  • PMID:23460508
DOID:0112361 spondylocostal dysostosis 3 HGNC:6560 Homo sapiens (human) 3955 LFNG
  • RGD:7240710
DOID:10966 lipoid nephrosis HGNC:6561 Homo sapiens (human) 3956 LGALS1
  • MGI:6194238
DOID:707 B-cell lymphoma HGNC:6561 Homo sapiens (human) 3956 LGALS1
  • MGI:6194238
DOID:13619 extrahepatic cholestasis HGNC:6561 Homo sapiens (human) 3956 LGALS1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:6562 Homo sapiens (human) 3957 LGALS2
  • PMID:15129282
  • RGD:7240710
DOID:219 colon cancer HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:0080600 COVID-19 HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • PMID:35115644
DOID:3021 acute kidney failure HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:1094 attention deficit hyperactivity disorder HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:1712 aortic valve stenosis HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • PMID:15520318
DOID:9744 type 1 diabetes mellitus HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:2841 asthma HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • PMID:16424226
DOID:5082 liver cirrhosis HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • PMID:16549783
DOID:3070 high grade glioma HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:10763 hypertension HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:2316 brain ischemia HGNC:6563 Homo sapiens (human) 3958 LGALS3
  • MGI:6194238
DOID:14502 cholesterol ester storage disease HGNC:6617 Homo sapiens (human) 3988 LIPA
  • PMID:6097111
  • RGD:7240710
DOID:0080217 lysosomal acid lipase deficiency HGNC:6617 Homo sapiens (human) 3988 LIPA
  • MGI:6194238
DOID:14497 Wolman disease HGNC:6617 Homo sapiens (human) 3988 LIPA
  • MGI:6194238
  • PMID:6097111
  • PMID:8146180
  • RGD:7240710
DOID:2018 hyperinsulinism HGNC:6619 Homo sapiens (human) 3990 LIPC
  • MGI:6194238
  • PMID:11095452
  • PMID:1592086

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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