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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 69976 - 70000 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol ▼ FlyGlycoDB Evidence Code Names References
DOID:0060180 colitis HGNC:602 Homo sapiens (human) 337 APOA4
  • PMID:15254593
DOID:10652 Alzheimer's disease HGNC:602 Homo sapiens (human) 337 APOA4
  • PMID:10559562
  • PMID:16013913
  • PMID:9272683
DOID:1389 polyneuropathy HGNC:602 Homo sapiens (human) 337 APOA4
  • PMID:19589605
DOID:2378 relapsing-remitting multiple sclerosis HGNC:602 Homo sapiens (human) 337 APOA4
  • PMID:19383442
DOID:13809 familial combined hyperlipidemia HGNC:601 Homo sapiens (human) 336 APOA2
  • PMID:12738753
DOID:9352 type 2 diabetes mellitus HGNC:601 Homo sapiens (human) 336 APOA2
  • PMID:19817643
  • PMID:9649952
DOID:9744 type 1 diabetes mellitus HGNC:601 Homo sapiens (human) 336 APOA2
  • PMID:9578960
DOID:684 hepatocellular carcinoma HGNC:601 Homo sapiens (human) 336 APOA2
  • PMID:31211449
DOID:9970 obesity HGNC:601 Homo sapiens (human) 336 APOA2
  • PMID:9002300
DOID:7998 hyperthyroidism HGNC:601 Homo sapiens (human) 336 APOA2
  • MGI:6194238
DOID:3393 coronary artery disease HGNC:601 Homo sapiens (human) 336 APOA2
  • PMID:17923573
DOID:1184 nephrotic syndrome HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:2671 transitional cell carcinoma HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
  • PMID:21496341
DOID:9074 systemic lupus erythematosus HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:20131231
DOID:14330 Parkinson's disease HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:20085559
DOID:1387 hypolipoproteinemia HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:9931341
DOID:1793 pancreatic cancer HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:17312459
  • PMID:17332923
DOID:13810 familial hypercholesterolemia HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:9699897
DOID:11446 sciatic neuropathy HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:9452 steatotic liver disease HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:1883 hepatitis C HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:19818291
DOID:1470 major depressive disorder HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:10652 Alzheimer's disease HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:19863188
  • PMID:20847045
DOID:10763 hypertension HGNC:600 Homo sapiens (human) 335 APOA1
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus HGNC:600 Homo sapiens (human) 335 APOA1
  • PMID:18079481
  • PMID:9649952

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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