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 9276 - 9300 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:23064 Homo sapiens (human) 119391 GSTO2
  • MGI:6194238
DOID:2841 asthma HGNC:23064 Homo sapiens (human) 119391 GSTO2
  • PMID:20374258
DOID:10584 retinitis pigmentosa HGNC:23059 Homo sapiens (human) 63827 BCAN
  • PMID:29150673
DOID:3525 middle cerebral artery infarction HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
DOID:3070 high grade glioma HGNC:23059 Homo sapiens (human) 63827 BCAN
  • MGI:6194238
  • PMID:16061654
  • PMID:23253190
DOID:5212 congenital disorder of glycosylation HGNC:23056 Homo sapiens (human) 10195 ALG3
  • MGI:6194238
DOID:0080556 congenital disorder of glycosylation Id HGNC:23056 Homo sapiens (human) 10195 ALG3
  • MGI:6194238
  • RGD:7240710
DOID:3343 glycoproteinosis HGNC:23026 Homo sapiens (human) 84572 GNPTG
  • PMID:10712439
DOID:0080678 mucolipidosis III gamma HGNC:23026 Homo sapiens (human) 84572 GNPTG
  • RGD:7240710
DOID:0060174 GABA aminotransferase deficiency HGNC:23 Homo sapiens (human) 18 ABAT
  • RGD:7240710
DOID:10763 hypertension HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:9976 heroin dependence HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:11832 visual epilepsy HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:0080855 Parkinsonism HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:23 Homo sapiens (human) 18 ABAT
  • PMID:1627256
DOID:2548 reflex epilepsy HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:0050562 West syndrome HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:12858 Huntington's disease HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
  • PMID:6237280
DOID:1824 status epilepticus HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:1596 depressive disorder HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:326 ischemia HGNC:23 Homo sapiens (human) 18 ABAT
  • MGI:6194238
DOID:0060256 Dowling-Degos disease HGNC:22954 Homo sapiens (human) 56983 POGLUT1
  • RGD:7240710
DOID:0080762 autosomal recessive limb-girdle muscular dystrophy type 2Z HGNC:22954 Homo sapiens (human) 56983 POGLUT1
  • RGD:7240710
DOID:0110274 autosomal recessive limb-girdle muscular dystrophy HGNC:22954 Homo sapiens (human) 56983 POGLUT1
  • MGI:6194238
DOID:0112374 muscular dystrophy-dystroglycanopathy HGNC:22932 Homo sapiens (human) 29925 GMPPB
  • PMID:26310427

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