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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 October 9, 2024
Displaying entries 61401 - 61425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:326 ischemia HGNC:2358 Homo sapiens (human) 1395 CRHR2
  • MGI:6194238
DOID:0060180 colitis HGNC:2358 Homo sapiens (human) 1395 CRHR2
  • MGI:6194238
DOID:9778 irritable bowel syndrome HGNC:2358 Homo sapiens (human) 1395 CRHR2
  • MGI:6194238
DOID:2841 asthma HGNC:2358 Homo sapiens (human) 1395 CRHR2
  • PMID:18408560
DOID:1596 depressive disorder HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • MGI:6194238
DOID:4483 rhinitis HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • PMID:17597629
DOID:9970 obesity HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • PMID:14724656
DOID:0050696 fetal alcohol spectrum disorder HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • MGI:6194238
DOID:3877 functional colonic disease HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • MGI:6194238
DOID:2841 asthma HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • PMID:16113459
  • PMID:19663668
DOID:12918 thromboangiitis obliterans HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • MGI:6194238
DOID:3083 chronic obstructive pulmonary disease HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • PMID:19210659
DOID:9778 irritable bowel syndrome HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • MGI:6194238
DOID:10763 hypertension HGNC:2357 Homo sapiens (human) 1394 CRHR1
  • MGI:6194238
DOID:9970 obesity HGNC:2356 Homo sapiens (human) 1393 CRHBP
  • MGI:6194238
DOID:3328 temporal lobe epilepsy HGNC:2356 Homo sapiens (human) 1393 CRHBP
  • MGI:6194238
DOID:1596 depressive disorder HGNC:2356 Homo sapiens (human) 1393 CRHBP
  • MGI:6194238
  • PMID:14573312
DOID:0050651 atrioventricular septal defect HGNC:14630 Homo sapiens (human) 78987 CRELD1
  • RGD:7240710
DOID:1681 heart septal defect HGNC:14630 Homo sapiens (human) 78987 CRELD1
  • PMID:12632326
DOID:1574 alcohol use disorder HGNC:2348 Homo sapiens (human) 1387 CREBBP
  • MGI:6194238
DOID:9119 acute myeloid leukemia HGNC:2348 Homo sapiens (human) 1387 CREBBP
  • MGI:6194238
  • PMID:12461753
DOID:12858 Huntington's disease HGNC:2348 Homo sapiens (human) 1387 CREBBP
  • PMID:11264541
DOID:0060041 autism spectrum disorder HGNC:2348 Homo sapiens (human) 1387 CREBBP
  • MGI:6194238
DOID:0050908 myelodysplastic syndrome HGNC:2348 Homo sapiens (human) 1387 CREBBP
  • MGI:6194238

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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: December 9, 2024