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 10076 - 10100 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3498 pancreatic ductal adenocarcinoma FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:684 hepatocellular carcinoma FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:10534 stomach cancer FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:8584 Burkitt lymphoma FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:169 neuroendocrine tumor FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:1520 colon carcinoma FB:FBgn0005585 Drosophila melanogaster (fruit fly) 41166 Calr CG9429
  • MGI:6194238
DOID:13619 extrahepatic cholestasis HGNC:2653 Homo sapiens (human) 1582 CYP8B1
  • MGI:6194238
DOID:10787 premature menopause HGNC:2653 Homo sapiens (human) 1582 CYP8B1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:2653 Homo sapiens (human) 1582 CYP8B1
  • MGI:6194238
DOID:0111070 congenital bile acid synthesis defect 3 HGNC:2652 Homo sapiens (human) 9420 CYP7B1
  • RGD:7240710
DOID:0110810 hereditary spastic paraplegia 5A HGNC:2652 Homo sapiens (human) 9420 CYP7B1
  • RGD:7240710
DOID:13619 extrahepatic cholestasis HGNC:2651 Homo sapiens (human) 1581 CYP7A1
  • MGI:6194238
DOID:13580 cholestasis HGNC:2651 Homo sapiens (human) 1581 CYP7A1
  • MGI:6194238
DOID:12351 alcoholic hepatitis HGNC:2651 Homo sapiens (human) 1581 CYP7A1
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:2651 Homo sapiens (human) 1581 CYP7A1
  • MGI:6194238
  • PMID:28774887
DOID:10283 prostate cancer HGNC:2649 Homo sapiens (human) 1595 CYP51A1
  • MGI:6194238
DOID:9351 diabetes mellitus HGNC:2649 Homo sapiens (human) 1595 CYP51A1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2649 Homo sapiens (human) 1595 CYP51A1
  • MGI:6194238
DOID:10763 hypertension HGNC:2648 Homo sapiens (human) 11283 CYP4F8
  • MGI:6194238
DOID:0050861 colorectal adenocarcinoma HGNC:2648 Homo sapiens (human) 11283 CYP4F8
  • PMID:27354594
DOID:10763 hypertension HGNC:2645 Homo sapiens (human) 8529 CYP4F2
  • MGI:6194238
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:20575 Homo sapiens (human) 284541 CYP4A22
  • MGI:6194238
DOID:10763 hypertension HGNC:20575 Homo sapiens (human) 284541 CYP4A22
  • MGI:6194238
DOID:10763 hypertension HGNC:2642 Homo sapiens (human) 1579 CYP4A11
  • MGI:6194238
  • PMID:16144986
DOID:0110861 autosomal recessive polycystic kidney disease HGNC:2642 Homo sapiens (human) 1579 CYP4A11
  • 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