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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 8876 - 8900 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:10283 prostate cancer HGNC:2665 Homo sapiens (human) 1604 CD55
  • PMID:16533428
  • PMID:18288643
DOID:10611 protein-losing enteropathy HGNC:2665 Homo sapiens (human) 1604 CD55
  • RGD:7240710
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:12801 mucopolysaccharidosis III HGNC:26527 Homo sapiens (human) 138050 HGSNAT
  • MGI:6194238
DOID:0110389 retinitis pigmentosa 73 HGNC:26527 Homo sapiens (human) 138050 HGSNAT
  • RGD:7240710
DOID:0111393 mucopolysaccharidosis type IIIC HGNC:26527 Homo sapiens (human) 138050 HGSNAT
  • RGD:7240710
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: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
DOID:10652 Alzheimer's disease HGNC:2641 Homo sapiens (human) 10858 CYP46A1
  • PMID:12232784
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • PMID:21225912
DOID:9952 acute lymphoblastic leukemia HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • PMID:19650988
  • PMID:22215203

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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