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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 10651 - 10675 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:3393 coronary artery disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:15115767
  • PMID:17070179
DOID:9352 type 2 diabetes mellitus HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22399516
DOID:7148 rheumatoid arthritis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:17326817
DOID:12554 hemolytic-uremic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:10873870
DOID:1184 nephrotic syndrome HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • MGI:6194238
  • PMID:15292677
DOID:783 end stage renal disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:16421163
DOID:7693 abdominal aortic aneurysm HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:11807372
DOID:1936 atherosclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:12590019
DOID:13001 carotid stenosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22075154
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22112193
DOID:0050848 obstructive sleep apnea HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:21698055
DOID:2377 multiple sclerosis HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22246459
DOID:2841 asthma HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:10733466
DOID:3407 carotid artery disease HGNC:9040 Homo sapiens (human) 7941 PLA2G7
  • PMID:22499993
DOID:891 progressive myoclonus epilepsy HGNC:3413 Homo sapiens (human) 7957 EPM2A
  • PMID:9771710
DOID:3534 Lafora disease HGNC:3413 Homo sapiens (human) 7957 EPM2A
  • MGI:6194238
DOID:1508 candidiasis ZFIN:ZDB-GENE-080723-75 Danio rerio (zebrafish) 796410 fut9a
  • MGI:6194238
DOID:0080568 congenital disorder of glycosylation Iq HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • RGD:7240710
DOID:0050570 congenital disorder of glycosylation type I HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • MGI:6194238
DOID:0050807 Kahrizi syndrome HGNC:25812 Homo sapiens (human) 79644 SRD5A3
  • RGD:7240710
DOID:0070352 stress-induced childhood-onset neurodegeneration with variable ataxia and seizures ZFIN:ZDB-GENE-040912-85 Danio rerio (zebrafish) 796446 adprs
  • MGI:6194238
DOID:1574 alcohol use disorder HGNC:14942 Homo sapiens (human) 79660 PPP1R3B
  • MGI:6194238
DOID:9970 obesity HGNC:18448 Homo sapiens (human) 79661 NEIL1
  • MGI:6194238
DOID:0060611 abdominal obesity-metabolic syndrome HGNC:18448 Homo sapiens (human) 79661 NEIL1
  • MGI:6194238
DOID:594 panic disorder HGNC:21072 Homo sapiens (human) 79694 MANEA
  • PMID:24473444

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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