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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 10326 - 10350 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3454 brain infarction HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
DOID:10591 pre-eclampsia HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:15569322
DOID:0050891 adrenal cortical adenoma HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:12457455
DOID:0080626 corticosterone methyloxidase deficiency 1 HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • RGD:7240710
DOID:446 primary hyperaldosteronism HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:1731223
DOID:0050811 congenital adrenal hyperplasia HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:18771471
DOID:9351 diabetes mellitus HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • PMID:11687612
DOID:10763 hypertension HGNC:2592 Homo sapiens (human) 1585 CYP11B2
  • MGI:6194238
  • PMID:10024332
DOID:3454 brain infarction HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:10763 hypertension HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:446 primary hyperaldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • PMID:1731223
DOID:0050891 adrenal cortical adenoma HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • PMID:12457455
DOID:114 heart disease HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:5844 myocardial infarction HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:820 myocarditis HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:0050811 congenital adrenal hyperplasia HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
  • PMID:1430088
  • PMID:8964882
DOID:14080 glucocorticoid-remediable aldosteronism HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • RGD:7240710
DOID:14219 renal tubular acidosis HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:6000 congestive heart failure HGNC:2591 Homo sapiens (human) 1584 CYP11B1
  • MGI:6194238
DOID:1824 status epilepticus HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:1924 hypogonadism HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:10763 hypertension HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • MGI:6194238
DOID:0050546 congenital adrenal insufficiency HGNC:2590 Homo sapiens (human) 1583 CYP11A1
  • RGD:7240710

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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