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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 6701 - 6725 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID ▼ Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names References
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:0110736 neurodegeneration with brain iron accumulation 2b HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • RGD:7240710
DOID:0060900 Parkinson's disease 14 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
  • RGD:7240710
DOID:0110735 neurodegeneration with brain iron accumulation 2a HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
  • PMID:22934738
  • RGD:7240710
DOID:10247 pleurisy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
DOID:2367 neuroaxonal dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:17033970
  • PMID:19138334
DOID:0090056 dystonia 12 HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:19087156
DOID:11723 Duchenne muscular dystrophy HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:22934738
DOID:14330 Parkinson's disease HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • PMID:20938027
  • PMID:21368765
DOID:1289 neurodegenerative disease HGNC:9039 Homo sapiens (human) 8398 PLA2G6
  • MGI:6194238
DOID:0111677 familial benign fleck retina HGNC:9038 Homo sapiens (human) 5322 PLA2G5
  • RGD:7240710
DOID:4195 hyperglycemia HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:2671 transitional cell carcinoma HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:2841 asthma HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:2615 papilloma HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:2316 brain ischemia HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:0080322 polycystic kidney disease HGNC:9035 Homo sapiens (human) 5321 PLA2G4A
  • MGI:6194238
DOID:11204 allergic conjunctivitis HGNC:9031 Homo sapiens (human) 5320 PLA2G2A
  • PMID:21042565

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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