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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 70001 - 70025 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:5844 myocardial infarction HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:10428310
  • PMID:20176799
DOID:9282 ocular hypertension HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:684 hepatocellular carcinoma HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:23935864
  • PMID:31211449
DOID:6000 congestive heart failure HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:17517342
DOID:2377 multiple sclerosis HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:20350318
DOID:0050156 idiopathic pulmonary fibrosis HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:20463180
DOID:783 end stage renal disease HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:18079481
  • PMID:22515595
DOID:7998 hyperthyroidism HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:11512 Budd-Chiari syndrome HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:21145806
DOID:1936 atherosclerosis HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:18287885
  • PMID:23078847
DOID:3393 coronary artery disease HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:2128269
DOID:2349 arteriosclerosis HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:0080547 metabolic dysfunction-associated steatohepatitis HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
  • PMID:24793484
DOID:9970 obesity HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:12725089
DOID:0080958 primary hypoalphalipoproteinemia 2 HGNC:600 Homo sapiens (human) 335 APOA1
  • RGD:7240710
DOID:9744 type 1 diabetes mellitus HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:9578960
DOID:4947 cholangiocarcinoma HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:19486127
DOID:687 hepatoblastoma HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:27974108
DOID:5409 lung small cell carcinoma HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:26996551
DOID:5082 liver cirrhosis HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:27106140
DOID:0080348 Alzheimer's disease 1 HGNC:598 Homo sapiens (human) 334 APLP2
  • MGI:6194238
DOID:1289 neurodegenerative disease HGNC:598 Homo sapiens (human) 334 APLP2
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:598 Homo sapiens (human) 334 APLP2
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:597 Homo sapiens (human) 333 APLP1
  • MGI:6194238
DOID:0080348 Alzheimer's disease 1 HGNC:597 Homo sapiens (human) 333 APLP1
  • MGI:6194238

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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: December 9, 2024