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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 71401 - 71425 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:9744 type 1 diabetes mellitus HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2658981
DOID:2377 multiple sclerosis HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:2953866
DOID:9976 heroin dependence HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:31129131
DOID:437 myasthenia gravis HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:17986328
DOID:14330 Parkinson's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:19474411
DOID:10652 Alzheimer's disease HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:16581404
DOID:2297 leptospirosis HGNC:108 Homo sapiens (human) 43 ACHE
  • MGI:6194238
DOID:1849 cannabis dependence HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:31129131
DOID:1826 epilepsy HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:7634486
DOID:9974 drug dependence HGNC:108 Homo sapiens (human) 43 ACHE
  • PMID:31129131
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:16066 Homo sapiens (human) 55331 ACER3
  • PMID:31949129
DOID:10579 leukodystrophy HGNC:16066 Homo sapiens (human) 55331 ACER3
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:16066 Homo sapiens (human) 55331 ACER3
  • PMID:30097213
DOID:6000 congestive heart failure HGNC:13557 Homo sapiens (human) 59272 ACE2
  • MGI:6194238
  • PMID:32227090
DOID:11984 hypertrophic cardiomyopathy HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:32448590
DOID:1273 respiratory syncytial virus infectious disease HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:26813885
DOID:6432 pulmonary hypertension HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:25225206
DOID:4492 avian influenza HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:24800825
DOID:0060903 thrombosis HGNC:13557 Homo sapiens (human) 59272 ACE2
  • MGI:6194238
DOID:0080600 COVID-19 HGNC:13557 Homo sapiens (human) 59272 ACE2
  • MGI:6194238
  • PMID:32220422
  • PMID:32380511
  • PMID:34668775
  • PMID:34668780
DOID:2945 severe acute respiratory syndrome HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:17974127
  • PMID:32553273
DOID:8947 diabetic retinopathy HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:21792177
  • PMID:31380462
DOID:12236 primary biliary cholangitis HGNC:13557 Homo sapiens (human) 59272 ACE2
  • MGI:6194238
DOID:3587 pancreatic ductal carcinoma HGNC:13557 Homo sapiens (human) 59272 ACE2
  • PMID:19212105
DOID:5844 myocardial infarction HGNC:13557 Homo sapiens (human) 59272 ACE2
  • 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