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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 71376 - 71400 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:3571 liver cancer HGNC:24436 Homo sapiens (human) 134526 ACOT12
  • MGI:6194238
DOID:1891 optic nerve disease HGNC:118 Homo sapiens (human) 50 ACO2
  • 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
DOID:0050883 infantile cerebellar-retinal degeneration HGNC:118 Homo sapiens (human) 50 ACO2
  • MGI:6194238
  • RGD:7240710
DOID:14330 Parkinson's disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • MGI:6194238
DOID:0050883 infantile cerebellar-retinal degeneration SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • MGI:6194238
DOID:0111442 optic atrophy 9 SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • MGI:6194238
  • PMID:33028849
DOID:1724 duodenal ulcer HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:331 central nervous system disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • PMID:25351951
DOID:1289 neurodegenerative disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • PMID:25351951
DOID:1891 optic nerve disease SGD:S000004295 Saccharomyces cerevisiae S288C 851013 ACO1
  • PMID:25351951
DOID:13268 porphyria HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease HGNC:117 Homo sapiens (human) 48 ACO1
  • MGI:6194238
DOID:2600 laryngeal carcinoma HGNC:23692 Homo sapiens (human) 57007 ACKR3
  • PMID:16494043
DOID:4467 clear cell renal cell carcinoma HGNC:23692 Homo sapiens (human) 57007 ACKR3
  • PMID:29218250
DOID:12978 Plasmodium vivax malaria HGNC:4035 Homo sapiens (human) 2532 ACKR1
  • RGD:7240710
DOID:12365 malaria HGNC:4035 Homo sapiens (human) 2532 ACKR1
  • RGD:7240710
DOID:9470 bacterial meningitis HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:21303225
DOID:12858 Huntington's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2953866
DOID:10487 Hirschsprung's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:21991983
DOID:8645 subacute delirium HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:8043620
DOID:6088 acute stress disorder HGNC:108 Homo sapiens (human) 43 ACHE
  • 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: December 9, 2024