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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 2101 - 2125 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:0080887 vitamin D-dependent rickets type 1B HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • MGI:6194238
  • RGD:7240710
DOID:3393 coronary artery disease HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • PMID:25003556
DOID:3454 brain infarction HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • PMID:36762557
DOID:9970 obesity HGNC:20580 Homo sapiens (human) 120227 CYP2R1
  • PMID:34906413
DOID:0110808 hereditary spastic paraplegia 56 HGNC:20582 Homo sapiens (human) 113612 CYP2U1
  • RGD:7240710
DOID:2987 familial mediterranean fever HGNC:2637 Homo sapiens (human) 1576 CYP3A4
  • PMID:23408444
DOID:1612 breast cancer HGNC:2637 Homo sapiens (human) 1576 CYP3A4
  • PMID:15180491
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
DOID:10825 essential hypertension HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • RGD:7240710
DOID:1596 depressive disorder HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • MGI:6194238
DOID:13580 cholestasis HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • MGI:6194238
DOID:783 end stage renal disease HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • MGI:6194238
DOID:8552 chronic myeloid leukemia HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • PMID:19584153
  • PMID:21039054
DOID:2030 anxiety disorder HGNC:2638 Homo sapiens (human) 1577 CYP3A5
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:2641 Homo sapiens (human) 10858 CYP46A1
  • PMID:12232784
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: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:2645 Homo sapiens (human) 8529 CYP4F2
  • 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: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

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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