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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 1626 - 1650 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:552 pneumonia HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:15928955
DOID:0050866 oral squamous cell carcinoma HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • PMID:22954124
DOID:3525 middle cerebral artery infarction HGNC:2631 Homo sapiens (human) 1571 CYP2E1
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
  • PMID:23155181
DOID:0050855 renal fibrosis HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • PMID:22260463
DOID:10952 nephritis HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • PMID:17126841
DOID:5199 ureteral obstruction HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
DOID:6432 pulmonary hypertension HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • PMID:20118222
DOID:1073 renal hypertension HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
  • PMID:20495177
DOID:874 bacterial pneumonia HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • MGI:6194238
DOID:10763 hypertension HGNC:2634 Homo sapiens (human) 1573 CYP2J2
  • PMID:17286575
  • PMID:20501636
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: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:13619 extrahepatic cholestasis HGNC:2651 Homo sapiens (human) 1581 CYP7A1
  • 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