Table Filtering
Other Information
Release Statistics Download
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 6201 - 6225 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:8127 Homo sapiens (human) 8473 OGT
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:8133 Homo sapiens (human) 4973 OLR1
  • PMID:12646194
  • RGD:7240710
DOID:783 end stage renal disease HGNC:8133 Homo sapiens (human) 4973 OLR1
  • MGI:6194238
DOID:9246 cerebral amyloid angiopathy HGNC:8133 Homo sapiens (human) 4973 OLR1
  • PMID:16328515
DOID:3393 coronary artery disease HGNC:8133 Homo sapiens (human) 4973 OLR1
  • PMID:12810610
  • PMID:15562935
DOID:10763 hypertension HGNC:8133 Homo sapiens (human) 4973 OLR1
  • MGI:6194238
DOID:2394 ovarian cancer HGNC:8143 Homo sapiens (human) 4978 OPCML
  • RGD:7240710
DOID:2841 asthma HGNC:16036 Homo sapiens (human) 94101 ORMDL1
  • MGI:6194238
DOID:2841 asthma HGNC:16037 Homo sapiens (human) 29095 ORMDL2
  • MGI:6194238
DOID:0081183 autosomal recessive intellectual developmental disorder 7 SGD:S000005611 Saccharomyces cerevisiae S288C 854252 OST3
  • MGI:6194238
DOID:0111839 congenital disorder of glycosylation Icc SGD:S000005611 Saccharomyces cerevisiae S288C 854252 OST3
  • MGI:6194238
DOID:10283 prostate cancer SGD:S000005611 Saccharomyces cerevisiae S288C 854252 OST3
  • MGI:6194238
DOID:0080319 X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia SGD:S000005611 Saccharomyces cerevisiae S288C 854252 OST3
  • MGI:6194238
DOID:612 primary immunodeficiency disease SGD:S000005611 Saccharomyces cerevisiae S288C 854252 OST3
  • MGI:6194238
DOID:104 bacterial infectious disease SGD:S000005611 Saccharomyces cerevisiae S288C 854252 OST3
  • MGI:6194238
DOID:0110480 autosomal recessive nonsyndromic deafness 22 HGNC:16378 Homo sapiens (human) 146183 OTOA
  • MGI:6194238
  • RGD:7240710
DOID:0110474 autosomal recessive nonsyndromic deafness 18B HGNC:8516 Homo sapiens (human) 340990 OTOG
  • MGI:6194238
  • RGD:7240710
DOID:2978 carbohydrate metabolic disorder HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • PMID:8844009
DOID:9352 type 2 diabetes mellitus HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • MGI:6194238
DOID:9970 obesity HGNC:8527 Homo sapiens (human) 5019 OXCT1
  • MGI:6194238
DOID:612 primary immunodeficiency disease RGD:621760 Rattus norvegicus (Norway rat) 192281 Oas1a
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus RGD:621077 Rattus norvegicus (Norway rat) 154968 Oga
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus FB:FBgn0038870 Drosophila melanogaster (fruit fly) 42518 Oga CG5871
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus MGI:1932139 Mus musculus (house mouse) 76055 Oga
  • MGI:6194238
DOID:0081326 oxoglutarate dehydrogenase deficiency RGD:1561359 Rattus norvegicus (Norway rat) 360975 Ogdh
  • MGI:6194238

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024