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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 151 - 175 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▲ FlyGlycoDB Evidence Code Names References
DOID:10579 leukodystrophy HGNC:16066 Homo sapiens (human) 55331 ACER3
  • MGI:6194238
DOID:437 myasthenia gravis HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:17986328
DOID:12858 Huntington's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2953866
DOID:2377 multiple sclerosis HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2953866
DOID:1826 epilepsy HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:7634486
DOID:2297 leptospirosis HGNC:108 Homo sapiens (human) 43 ACHE
  • MGI:6194238
DOID:6088 acute stress disorder HGNC:108 Homo sapiens (human) 43 ACHE
  • MGI:6194238
DOID:9744 type 1 diabetes mellitus HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2658981
DOID:10652 Alzheimer's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:16581404
DOID:10487 Hirschsprung's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:21991983
DOID:9470 bacterial meningitis HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:21303225
DOID:14330 Parkinson's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:19474411
DOID:331 central nervous system disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • PMID:25351951
DOID:13268 porphyria HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:14330 Parkinson's disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • MGI:6194238
DOID:1289 neurodegenerative disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • PMID:25351951
DOID:0111442 optic atrophy 9 SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • MGI:6194238
  • PMID:33028849
DOID:1891 optic nerve disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • PMID:25351951
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:0050883 infantile cerebellar-retinal degeneration SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • MGI:6194238
DOID:1724 duodenal ulcer HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:331 central nervous system disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:0111442 optic atrophy 9 HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:14330 Parkinson's disease HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:118 Homo sapiens (human) 50 ACO2
  • 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