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 1501 - 1525 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▲ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:1612 breast cancer HGNC:10850 Homo sapiens (human) 6470 SHMT1
  • PMID:17896178
DOID:162 cancer HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:5419 schizophrenia HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:10852 Homo sapiens (human) 6472 SHMT2
  • MGI:6194238
DOID:0060180 colitis HGNC:10856 Homo sapiens (human) 6476 SI
  • MGI:6194238
DOID:0111633 congenital sucrase-isomaltase deficiency HGNC:10856 Homo sapiens (human) 6476 SI
  • RGD:7240710
DOID:3070 high grade glioma HGNC:10860 Homo sapiens (human) 6480 ST6GAL1
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:10860 Homo sapiens (human) 6480 ST6GAL1
  • PMID:17697868
DOID:0081180 autosomal recessive intellectual developmental disorder 12 HGNC:10866 Homo sapiens (human) 6487 ST3GAL3
  • RGD:7240710
DOID:0080414 developmental and epileptic encephalopathy 15 HGNC:10866 Homo sapiens (human) 6487 ST3GAL3
  • RGD:7240710
DOID:0060470 salt and pepper syndrome HGNC:10872 Homo sapiens (human) 8869 ST3GAL5
  • RGD:7240710
DOID:9975 cocaine dependence HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3669 intermittent claudication HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:3070 high grade glioma HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:10886 Homo sapiens (human) 22933 SIRT2
  • MGI:6194238
DOID:0111630 familial erythrocytosis 8 HGNC:1093 Homo sapiens (human) 669 BPGM
  • PMID:1421379
  • RGD:7240710
DOID:3211 lysosomal storage disease HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
DOID:3659 sialuria HGNC:10933 Homo sapiens (human) 26503 SLC17A5
  • MGI:6194238
  • PMID:10581036
  • RGD:7240710
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures HGNC:1094 Homo sapiens (human) 670 BPHL
  • MGI:6194238
DOID:5742 pancreatic acinar cell adenocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:25266736
DOID:1793 pancreatic cancer HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:22871572
DOID:0080550 Noonan syndrome with multiple lentigines 3 HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710
DOID:1909 melanoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
  • PMID:16424035
  • PMID:22319199
  • PMID:25393105
  • PMID:25623140
DOID:3070 high grade glioma HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
DOID:9256 colorectal cancer HGNC:1097 Homo sapiens (human) 673 BRAF
  • RGD:7240710

About Release Notes Help Feedback

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